About Chapter 1: Acids and Bases Notes – Class 10 Chemistry
Acids and bases form the foundation of Chemistry at the Class 10 level, as they are used in everyday life, industries, laboratories, and nature. Acids are substances that produce hydrogen ions in aqueous solution, while bases release hydroxide ions. The study of their properties, reactions, and uses makes this chapter highly significant for board exams and competitive preparation. Acids are categorised as strong acids like hydrochloric acid and sulphuric acid, and weak acids like acetic acid and carbonic acid. Their strength depends on the extent of ionisation in water. Bases are also classified into strong bases, such as sodium hydroxide and potassium hydroxide, and weak bases like ammonium hydroxide. Indicators such as litmus, phenolphthalein, and methyl orange are commonly used to distinguish between acids and bases. One must go through the NCERT textbook for class 10 and solve the questions with the help of the NCERT solutions for class 10 science.
The chemical properties of acids include their reaction with metals producing hydrogen gas, with bases forming salt and water neutralisation, and with carbonates releasing carbon dioxide. Bases, on the other hand, react with oils and fats to form soap in a process called saponification. Neutralisation reaction between acid and base is an essential concept, as it helps explain the maintenance of pH balance in the human body, soil, and environment. The pH scale ranges from 0 to 14, where values less than 7 indicate acidic solutions, greater than 7 indicate basic solutions, and 7 represents neutral substances. The importance of pH can be seen in agriculture (soil treatment with lime to reduce acidity), medicine (antacids to relieve acidity), and daily life (shampoos and detergents designed for suitable pH levels). Natural indicators such as turmeric and red cabbage juice change colour depending on acidity or basicity, making them effective alternatives to chemical indicators. Industrial uses of acids include the manufacture of fertilisers, explosives, and dyes, while bases are used in soap, detergent, and paper industries.
Environmental concerns also connect to this topic, with acid rain caused by oxides of sulphur and nitrogen lowering the pH of soil and water bodies, affecting aquatic life and vegetation. Proper control of industrial emissions is necessary to reduce their harmful effects. In summary, the chapter Acids and Bases develops conceptual clarity about chemical behaviour, reactions, pH significance, industrial applications, and environmental impact, making it a vital topic for board preparation.
What Are Acids?
Acids are substances that release hydrogen ions (H⁺) when dissolved in aqueous solution. The sour taste of lemon juice, vinegar, and spoiled milk results from their acidic nature. According to the modern definition, an acid is characterized by its ability to donate protons (H⁺ ions) in water.
Acids are classified into two main categories based on their source:
Mineral Acids are derived from rocks and minerals. Examples include hydrochloric acid (HCl), sulfuric acid (H₂SO₄), and nitric acid (HNO₃). These acids find extensive use in industrial applications, from manufacturing fertilizers to petroleum refining.
Organic Acids occur naturally in plants and animals. Acetic acid in vinegar, citric acid in citrus fruits, and lactic acid in curd are common examples. These acids typically have weaker acidic properties compared to mineral acids.
Physical and Chemical Properties of Acids
Acids exhibit distinctive physical properties: they turn blue litmus paper red, change methyl orange to pink, and keep phenolphthalein colorless. Their aqueous solutions conduct electricity due to the presence of ions, and most possess corrosive properties that can damage skin and other materials.
The chemical behavior of acids becomes evident through several characteristic reactions. When acids react with metals, they produce salts and hydrogen gas a displacement reaction where more active metals displace hydrogen from the acid. For instance, zinc reacting with dilute sulfuric acid produces zinc sulfate and hydrogen gas, which burns with a characteristic "pop" sound.
Understanding Bases and Their Properties
Bases are substances that release hydroxide ions (OH⁻) in aqueous solution. They typically have a bitter taste and slippery, soapy feel. Water-soluble bases are specifically called alkalies, such as sodium hydroxide (NaOH) and potassium hydroxide (KOH).
Bases demonstrate opposite indicator behaviors to acids: they turn red litmus paper blue, change methyl orange to yellow, and turn phenolphthalein pink. Like acids, base solutions conduct electricity due to ionic dissociation.
Acid Strength and Ionization
The strength of an acid depends on its degree of ionization in water.
- Strong acids like HCl, HNO₃, and H₂SO₄ ionize completely, producing large concentrations of H⁺ ions.
- Weak acids such as acetic acid (CH₃COOH) and carbonic acid (H₂CO₃) only partially ionize, resulting in lower H⁺ concentrations.
This distinction is crucial: higher H⁺ concentration corresponds to greater acidic strength. Diluting an acid decreases its H⁺ concentration and reduces its strength—a principle important for safe laboratory practices.
The pH Scale: Measuring Acidity and Basicity
The pH scale provides a quantitative measure of hydrogen ion concentration in solutions. Developed by S.P.L. Sorensen, pH stands for "power of hydrogen" and ranges from 0 to 14.
The mathematical definition of pH is:
pH = -log[H⁺] or pH = -log[H₃O⁺]
This logarithmic scale means:
- pH < 7: Acidic solution
- pH = 7: Neutral solution (pure water)
- pH 7: Basic/alkaline solution
Each pH unit represents a tenfold change in hydrogen ion concentration. A solution with pH 3 is 1,000 times more acidic than one with pH 6. This logarithmic relationship makes the pH scale particularly useful for expressing the wide range of acidity and basicity found in everyday substances.
pH in Daily Life
The pH concept has practical significance across multiple domains. Human blood maintains a narrow pH range of 7.36-7.42, regulated by bicarbonates and carbonic acid acting as buffers. Gastric juice in the stomach has pH 1.0-3.0, enabling food digestion while potentially causing discomfort when produced in excess.
Tooth enamel, composed of calcium phosphate, remains stable at normal pH but corrodes when mouth pH drops below 5.5 typically due to bacterial acid production from sugar. This explains why dentists recommend limiting sugary foods and using basic toothpastes to neutralize acid.
Neutralization Reactions
Neutralization occurs when an acid reacts with a base to produce salt and water:
Acid + Base → Salt + Water
At the ionic level, this represents the combination of hydrogen ions from the acid with hydroxide ions from the base:
H⁺(aq) + OH⁻(aq) → H₂O(l)
These reactions are exothermic, releasing approximately 57.1 kJ of energy when strong acids react with strong bases. Neutralization has practical applications from treating acid indigestion with antacids to neutralizing insect stings.
Important Chemical Compounds
Sodium Chloride (Common Salt)
Sodium chloride (NaCl) serves as a fundamental compound beyond its culinary uses. Extracted from seawater through evaporation or mined as rock salt from underground deposits, it functions as the starting material for numerous chemicals including sodium hydroxide, washing soda, and baking soda.
Sodium Carbonate (Washing Soda)
Washing soda (Na₂CO₃·10H₂O) is manufactured through the Solvay process, starting with sodium chloride. The decahydrate form contains ten water molecules of crystallization. Upon air exposure, it effloresces, losing nine water molecules to form the monohydrate (Na₂CO₃ H₂O).
This compound finds use in glass manufacturing, water softening, and as a cleaning agent due to its basic properties.
Sodium Hydrogen Carbonate (Baking Soda)
Baking soda (NaHCO₃) is produced in the Solvay process by reacting sodium chloride with ammonia and carbon dioxide. When heated, it decomposes to form sodium carbonate, water, and carbon dioxide:
2NaHCO₃→ Na₂CO₃ + H₂O + CO₂
This carbon dioxide release makes baking soda essential in baking powder, where it causes dough to rise. It also serves as an antacid, neutralizing excess stomach acid.
Calcium Oxychloride (Bleaching Powder)
Bleaching powder (CaOCl₂) is prepared by passing chlorine gas over slaked lime at 313 K. Its bleaching action results from chlorine release. Applications include textile and paper bleaching, water disinfection, and chloroform manufacture.
Calcium Sulfate (Gypsum and Plaster of Paris)
Gypsum (CaSO₄ 2H₂O) contains two water molecules of crystallization. When heated to 373 K, it loses 1.5 water molecules to form Plaster of Paris (CaSO₄ 1/2 H₂O):
CaSO₄·2H₂O → CaSO₄ ½ H₂O + 1½H₂O
Plaster of Paris, when mixed with water, sets into a hard mass by rehydrating back to gypsum. This property makes it invaluable for medical casts, sculptural molds, and construction applications.
Formulas Reference Table
| Formula Name | Mathematical Expression | Explanation |
| pH Definition | pH = -log [H+] | Measures hydrogen ion concentration on logarithmic scale |
| Alternate pH | pH = -log[H3O+] | Equivalent expression using hydronium ion |
| Water Ionization | [H+][OH-] =10-4 at 298K | Ion product of water at standard temperature |
| Neutralization (Ionic) | H+(aq) + OH-(aq) → H2O(l) | Essential reaction between acid and base |
| Acid-Metal Reaction | Metal + Acid → Salt + H2 | General displacement reaction pattern |
| Acid-Carbonate Reaction | Carbonate + Acid → Salt + H2O + CO2 | Produces characteristic carbon dioxide gas |
| Gypsum Dehydration | CaSO4 . 2H2O → CaSO4 1/2 H2O + 1 1/2 H2O | Converts gypsum to Plaster of Paris |
| Baking Soda Decomposition | 2NaHCO3 → Na2CO3 + H2O + CO2 | Thermal decomposition releasing CO2 |
Indicators: Detecting Acids and Bases
Chemical indicators change color in response to pH changes, making them essential tools for identifying acidic or basic solutions.
- Litmus (extracted from lichens) turns red in acids and blue in bases.
- Phenolphthalein remains colorless in acids but turns pink in bases.
- Methyl orange appears pink in acids and yellow in bases.
- Universal indicators contain multiple dyes that produce different colors across the entire pH range (0-14), allowing quantitative pH determination through color comparison.
- Olfactory indicators represent an interesting category that distinguishes acids from bases through smell changes. Onion and vanilla extracts maintain their odor in acidic solutions but lose it in basic solutions, demonstrating the chemical interaction between bases and aromatic compounds.
Safe Handling and Dilution
Acid dilution requires careful technique due to the highly exothermic nature of the process. The cardinal rule: always add acid to water, never water to acid. Adding water to concentrated acid can cause violent boiling and splashing due to rapid heat generation, potentially causing severe burns.
When properly diluted by adding acid slowly to water with stirring, the heat dissipates safely into the larger water volume, preventing dangerous temperature spikes.
This comprehensive understanding of acids, bases, and salts forms the foundation for advanced chemistry studies and practical applications in industry, medicine, and everyday life. The concepts presented here from pH measurement to neutralization reactions demonstrate the systematic, predictable nature of chemical behavior governed by well-established principles.
Acids
Substances with sour taste are regarded as acids. Lemon juice, vinegar, grape fruit juice and spoilt milk etc. taste sour since they are acidic. Many substances can be identified as acids based on their taste but some of the acids like Sulphuric acid have very strong action on the skin which means that they are corrosive in nature. In such cases it would be according to modern definition
An acid may be defined as a substance which releases one or more H+ ions in aqueous solution.
Acids are mostly obtained from natural sources. On the basis of their source acids are of two types
(a) Mineral acids
(b) Organic acids
Mineral Acids:
Acids which are obtained from rocks and minerals are called mineral acids.
Organic Acids:
Acids which are present in animals and plants are known as organic acids. A list of commonly used acids along with their chemical formula and typical uses, is given below

| Name | Type | Chemical Formula | Where found or used |
| Carbonic acid | Mineral acid | H2CO3 | In soft drinks and lends fizz, In stomach as gastric juice, used in tanning industry |
| Nitric acid | Mineral acid | HNO3 | Used in the manufacture of explosives (TNT, Nitroglycerine) and fertilizers (Ammonium nitrate, Calcium nitrate, Purification of Au, Ag. |
| Hydrochloric acid | Mineral acid | HCl | In purification of common salt, in textile industry as bleaching agent, to make aqua regia. |
| Sulphuric acid | Mineral acid | H2SO4 | Commonly used in car batteries, in the manufacture of fertilizers (Ammonium sulphate, super phosphate) detergents etc, in paints, plastics, drugs, in manufacture of artificial silk, in petroleum refining. |
| Phosphoric acid | Mineral acid | H3PO4 | Used in antirust paints and in fertilizers. |
| Formic acid | Organic acid | HCOOH(CH2O2) | Found in the stings of ants and bees, used in tanning leather, in medicines for treating gout. |
| Acetic acid | Organic acid | CH3COOH(C2H4O2) | Found in vinegar, used as solvent in the manufacture of dyes and perfumes. |
| Lactic acid | Organic acid | CH3CH(OH)COOH(C3H6O3) | Responsible for souring of milk in curd. |
| Benzoic acid | Organic acid | C6H5COOH | Used as a food preservative. |
| Citric acid | Organic acid | C7H6O2 | Present in lemons, oranges and citrus fruits. |
Physical Propeties of Acids
(i) Sour taste: Almost all acidic substances have a sour taste.
(ii) Action on litmus solution: Acids turn blue litmus solution red.
(iii) Action on methyl orange: Acids turn methyl orange pink.
(iv) Action on phenolphthalein: Phenolphthalein remains colourless in acid.
(v) Conduction of electricity: The aqueous solution of acid conducts electricity.
(vi) Corrosive nature: Most acids are corrosive in nature. They produce a burning sensation on the skin and make holes on surfaces on which they fall.
Chemical Properties of Acids
Reaction of Acids with Metals:
When acid reacts with a metal, then a salt and hydrogen gas are formed.
i.e. Metal + Acid → Salt + Hydrogen gas
⇒ Reaction of dil with zinc metal.
Experiment: Take about 5 ml of dil H2SO4 in a test tube and add a few pieces of zinc granules in it. Pass the gas evolved through soap solution. The soap bubbles filled with gas rise.
Test for gas: Bring a burning candle near the gas filled soap bubble.
Observation: The gas present in soap bubble burns with pop sound which shows the gas evolved during reaction is hydrogen gas.

In this reaction more active metal zinc displaces less active hydrogen from H2SO4 and this hydrogen is evolved as gas.
Thus it is an example of displacement reaction. Some more examples of reaction of different metals with a particular acid:
Ex.:
Mg(s) + 2HCl(aq) → MgCl2(aq) + H2(g)
Magnesium + hydrochloric acid → magnesium chloride + hydrogen
(a metal) + (dil) → (a salt) + gas
Ex.:
Zn(s) + 2HCl(aq) → ZnCl2(aq) + H2(g)
zinc + hydrochloric acid → zinc chloride + hydrogen
(a metal) + (dil)→ (a salt) + gas
Ex.:
Fe(s) + 2HCl(aq) → FeCl2(aq) + H2(g)
iron + hydrochloric acid → iron(II) chloride + hydrogen
(a metal) + (dil) → (a salt) + gas
Ex.:
Cu + 2HCl(aq)→ no reaction
copper + hydrochloric acid
(a metal) + (dil)
The order of reactivities of above metals with same acid (dil HCl) is Mg > Zn > Fe > Cu i.e. these metals do not react with same acid with same vigour.
It is observed that at room temperature
(i) Mg reacts most vigorously
(ii) Zn reacts less vigorously than Mg
(iii) Fe reacts slowly
(iv) Cu does not react at all
Conclusion: From above reactions we reach to a conclusion that all metals do not react with same acid with same vigour.
The reason is the different reactivities or activities of metals towards acid.
In the above reactions we observe that metals like Mg, Fe, Zn being more active than hydrogen, displaces hydrogen from acid HCl and release H2 gas. Thus above reactions are displacement reactions, Cu being less reactive than hydrogen, cannot displace hydrogen from dil HCl. Thus no reaction takes place.
REACTION OF ACID WITH METAL CARBONATES AND METAL HYDROGEN CARBONATE (OR METAL BICARBONATES):
When an acid reacts with a metal carbonate or metal hydrogen carbonate (metal bicarbonate), then a salt, CO2 gas and H2O are formed.
i.e. Metal carbonate + Acid → Metal Salt + CO2 + H2O
Metal hydrogen carbonate (or metal bicarbonate) + Acid → Metal Salt + CO2 + H2O
⇒ Reaction of sodium carbonate (Na2CO3) or sodium hydrogen carbonate (NaHCO3) with dil HCl.
Experiment: Take about 0.5g of Na2CO3 or NaHCO3 in a test tube and add about 2 ml of dil HCl acid to it. Pass the gas evolved through lime water (taken in another test tube).
Observation: The lime water turns milky, showing that the gas evolved is CO2 gas.

Figure-Carbon dioxide gas (formed by the action of dil. HCl and Na2CO3) being passed through lime water
The reactions taking place are
Na2CO3(s) + 2HCl(aq) → 2NaCl(aq) + H2O(l) + CO2(g)
sodium carbonate hydrochloric acid sodium chloride water carbondioxide
(dil) (a salt)
Ca(OH2) (aq) + CO2(g) → CaCO3(s) + H2O(l)
lime water carbondioxide calcium carbonate water
(white ppt) (milky suspension)
Note:
(i) The lime water on passing CO2 gas turns milky due to formation of white ppt. of CaCO3 (insoluble in water) having milky appearance.
(ii) On passing excess of CO2 gas through lime water, milkiness disappears due to dissolution of white ppt of CaCO3 and clear solution is formed due to formation of soluble calcium bicarbonate [Ca(HCO3)2]
CaCO3(s) + H2O(l) + CO2(g) → Ca(HCO3)2(aq)
calcium carbonte water carbondioxide calcium bicarbonate
(white ppt)
(soluble in water) (insoluble in water) colourless
Ex.: MgCO3 (s) + 2HCl (aq) → MgCl2 (aq) + H2O (l) + CO2
(dil)
Mg(HCO3)2 (aq) + 2HCl (aq) → MgCl2 (aq) + 2H2O (l) + 2CO2
(dil)
Ex.: CaCO3 (s) + H2SO4(aq) → CaSO4(aq) + H2O (l) + CO2(g)
(dil)
Ca(HCO3)2(aq) + H2SO4(aq) → CaSO4(aq) + 2 H2O (l) + 2CO2(g)
(dil)
Ex.: ZnCO3 (s) + 2HCl (aq) → ZnCl2(aq) + H2O (l) + CO2(g)
(dil)
Zn(HCO3)2 (aq) + 2HCl(aq)→ ZnCl2(aq) + 2H2O (l) + 2CO2(g)
(dil)
REACTION OF ACIDS WITH BASES (NEUTRALIZATION REACTION)
When an acid reacts with a base then a salt and water are formed, i.e
Acid + Base → Salt + water
This reaction is called neutralization reaction, because when acid and base react with each other, they neutralize each other’s effect (i.e base destroys the acidic property of acid and acid destroys the basic property of base).
⇒ Reaction of hydrochloric acid (HCl) with sodium hydroxide (NaOH).
Experiment: Take about 10 ml of dil NaOH solution in a conical flask and add 2-3 drops of phenolphthalein indicator to it. The solution will turn pink (showing that it is basic in nature). Now add dil HCl solution from burette into flask slowly till the pink colour in the solution disappears.
Observation: This point (at which pink colour disappear) is called end point.
At end point:
(i) The dil NaOH solution in flask has been completely neutralised by dil HCl solution added from burette, dil NaOH has completely reacted with dil HCl.
(ii) [H+] = [OH–] (in case of NaOH & HCl)
(from acid) (from base)
The chemical reaction can be written as
NaOH (aq) + HCl (aq) → NaCl(aq) + H2O(l)
sodium hydroxide hydrochloric acid sodium chloride water
(base) (acid) (salt)
This reaction of acid and base to form salt and water is called neutralization reaction or neutralization of base by an acid

Figure-Neutralization of NaOH solution by HCl solution using phenolphthalein indicator
In the solution, NaOH, HCl and NaCl ionize completely into ions, so the above reaction can be written as:
Here's the text conversion with all mathematical symbols and expressions:
Na+ + OH- + H+ + Cl- → Na+ + Cl- + H2O
Canceling out the common ions on both sides, we get:
OH- + H+ →(neutralisation/Reaction)→ H2O
hydroxide ion hydrogen ion water (from base) (from acid)
Hence, neutralization may also be defined as the reaction between H+ ions given by acid with the OH- ions given by base to form water.
REACTION OF ACIDS WITH METALLIC OXIDES:
Acid react with metal oxide to form salt and water.
i.e. Metal oxide + Acid → Salt + Water
This reaction is similar to the neutralization reaction between acid and a base to form salt and water. Thus, the reaction between acids and metal oxides is a kind of neutralization reaction and shows that metallic oxides are basic oxides.
⇒ Reaction of copper (II) oxide with dilute hydrochloric acid:
Experiment: Take about 1- 2g of copper (II) oxide (black in colour) in a beaker. Add dil HCl slowly with constant stirring.
Observation: Black CuO dissolves in dil HCl and a bluish green solution is formed due to formation of copper (II) chloride (CuCl2) as salt.
The reaction taking place is:
Here is the text conversion of the chemical equation from the image:
CuO(s) + 2HCl(aq) → CuCl2(aq) + H2O
copper (II) oxide + hydrochloric acid → copper (II)chloride + water (black) (salt)
This represents a chemical reaction where solid copper (II) oxide reacts with aqueous hydrochloric acid to produce aqueous copper (II) chloride and water.
Note: In general Mineral Acids are Strong Acids while Organic Acids are Weak acids.
WHAT DO ALL ACIDS HAVE IN COMMON OR CHEMICAL NATURE OF ACIDS
⇒ To see what is common in all acids, let us perform the following experiment with different acids:
Experiment to illustrate chemical nature of acids or what do all acids have in common:
Take four test tubes and label them as A, B, C and D. Place them in a test tube stand. Take about 2 ml of each dil HCl, dil , dil and dil CH3COOH in test tubes A, B, C and D respectively. Now add few pieces of zinc granules in each test tube.

Observation: There is evolution of hydrogen gas (H2) in each test tube which burns with a pop sound on bringing a burning candle near the mouth of tubes.
Conclusion: Hydrogen is common in all acids i.e. all acids contain hydrogen which they liberate when they react with active metals.
Thus we can say that acids are the substances which contain hydrogen ion, which they liberate when they react with active metals.
All acids contain hydrogen but all hydrogen containing compounds are not acids, for example, glucose (C6H12O6) and alcohol (C2H5OH) contain hydrogen but they are not acids.
It can be explained more clearly by following experiment.
Experimentto show that all compounds containing hydrogen are not acids: The experiment is based on the fact that acids conduct electricity through their aqueous solutions.
(i) Take aqueous solutions of hydrogen containing compounds like hydrochloric acid (HCl), sulphuric acid , glucose and alcohol in 4 beakers respectively.
(ii) Fix two iron nails on the rubber cork and place the cork in each beaker
(iii) Connect the nails to the two terminals of a 6 volt battery through a switch and a bulb in each beaker as shown in the following figures.
(iv) Switch on the current in each case


Observation:
(i) Bulb starts glowing in arrangements (a) and (c) containing aqueous solutions of HCl and acids respectively.
It shows aqueous solutions of hydrochloric acid (HCl) and sulphuric acid (H2SO4) conduct electricity.
(ii) Aqueous solutions of glucose (C6H12O6) and alcohol (C2H5OH) do not conduct electricity (i.e. they do not allow electricity to pass through them) as bulb does not glow in arrangements b and d containing aqueous solutions of glucose and alcohol.
Explanation: Conduction of electricity through the aqueous solutions of acids (HCl and H2SO4) is due to the ions present in them. For example, aqueous solution of H2SO4 contains H+ and SO2-4 ions. These ions can carry electric current and thus are responsible for conduction of electricity through HCl and H2SO4 solutions. On the other hand aqueous solutions of glucose and alcohol (hydrogen containing compounds) do not contain H+ ions or any other ions. Due to absence of ions, aqueous solutions of glucose and alcohol do not conduct electricity.
Conclusion: From the above experiment, we lead to a conclusion that only those hydrogen containing compounds are acidic which when dissolved in water give H+ ions in the solution. Thus the definition of acid is modified as:
Acids are the substances which contain hydrogen and which when dissolved in water give H+ ions in the solution. This is called Arrhenius definition of acids given by Arrhenius in 1884.
WHAT HAPPENS TO AN ACID IN WATER SOLUTION?
It is observed that acidic behaviour of acids is due to the presence of H+ ions in them, which they give only in presence of water. So in the absence of water, a substance will not form ions and hence will not show its acidic behavior. It can be explained more clearly by following experiments:
Experiment: Take about 1–2 g of NaCl in a dry test tube. Add some concentrated into the test tube. Following reaction takes place producing hydrogen chloride (HCl) gas

Now bring a dry blue litmus paper and a wet (or moist) blue litmus paper near the mouth of test tube (which contains HCl gas)
Observation:
(i) The dry litmus paper does not turn red. It shows that HCl gas does not behave as an acid in absence of water (since there is no water in dry litmus paper).
(ii) The wet (or moist) litmus paper turns red. It shows that HCl gas acts as an acid only in presence of water (which is present in moist or wet litmus paper).
Explanation:
(i) When HCl gas come in contact with dry litmus paper, then HCl does not dissociate into ions (i.e H+ and Cl⁻ ions) due to absence of water in dry litmus paper.
Since H+ ions are responsible for acidic behaviour of acids, HCl gas does not show acidic behaviour with dry litmus paper and thus it does not turn the blue litmus red (due to absence of H+ ion in dry HCl gas).
HCl(g) in absence of water → Dissociation does not occur. (acts as gas)
(ii) When HCl gas comes in contact with wet litmus paper, then HCl dissociates into H⁺ and Cl⁻ ions due to dissociation of HCl in water present in wet litmus paper.
Since H+ ions are responsible for acidic behaviour of acids, HCl gas shows acidic behaviour with wet litmus paper and thus it turns it into red (due to presence of H+ ions in wet HCl gas) i.e.
HCl(g) in presence of water→ H+(aq) + Cl-(aq)
(acts as acid) (dissociation occurs)
Such dissociation of a covalent molecule like HCl into ions in the presence of water is called ionization. The ionization of HCl is shown more clearly as follows:

It is clear from the figure that, after dissociation of HCl, a number of water molecules remain attached to H+ and Cl-. Hence they are represented as H+(aq) and Cl-(aq) (aq indicating water molecules)
Alternatively, H+ ions combine with water molecule to form an ion called hydronium ion.
H+ + H2O → H3O+
hydrogen ion water molecule hydronium ion
Thus H+ does not exist freely in water, but exist in combination with water molecules. Hence, we represent it as H+(aq) or H3O+.
Conclusion: The properties of an acid is due to H+(aq) ions or hydronium ions (H3O+) which it gives in the aqueous solution.
or
Acidic properties of acids are due to presence of H+(aq) ions or H3O+ ions which they produce only in presence of water.
or
In absence of water, a substance will not form H+(aq) ions or H3O+ ions and hence will not show its acidic behaviour.
Classification of Acids on the Basis of Degree of Ionization or Strenght of Acids on the basis of degree of ionization
The acids are classified into two categories on the basis of the degree of ionization as follows:
- Strong acids
- Weak acids
STRONG ACID:
An acid which is completely ionized in water and thus produces a large amount of H+(aq) ions is called a strong acid e.g. acids like hydrochloric acid (HCl), nitric acid (HNO3) and sulphuric acid (H2SO4) are completely ionized in water and thus produce large amounts of H⁺(aq)ions in the solution. So these are called strong acids. The ionization of these acids are represented as follows:
(i) HCl + water→ H+(aq) + Cl-(aq) hydrochloric acid hydrogen ion chloride ion
or
HCl (aq) → H+ (aq) + Cl- (aq)
(ii) HNO3 + water → H+ (aq) + NO-3 (aq) nitric acid hydrogen ion nitrate ion
or
HNO3 (aq) → H+ (aq) + No3- (aq)
(iii) H2SO4 + water → 2H+(aq) + SO2-4 (aq) sulphuric acid hydrogen ion sulphate ion
or
H2SO4 (aq) → 2H+ (aq) + SO42- (aq)
Characteristics of strong acids:
Due to large amounts of H+(aq) ions in the solutions of strong acids,
(i) They react rapidly with other substances (such as metals, metal carbonates and metal hydrogen carbonates or metal bicarbonates).
(ii) They have a high electrical conductivity.
(iii) They are strong electrolytes.
Weak Acids:
An acid which is partially ionized in water and thus produces small amount of H+(aq) ions is called a weak acid. e.g. Acids like Acetic acid (CH3COOH) Formic acid (HCOOH), Carbonic acid (H2CO3) and Phosphoric acid (H3PO4) etc, are partially ionised in water and thus produce small amounts of H⁺(aq) ions in the solution, so these are called weak acids. The ionization of these acids are represented as follows:
(i) CH3COOH + water ⇌ CH3COO-(aq) + H+(aq)
Acetic acid Acetate ion Hydrogen ion
or
CH3COOH(aq) ⇌ CH3COO⁻(aq) + H+(aq)
(ii) H2CO3 + water ⇌ 2H+(aq) + CO32-(aq)
Carbonic acid Hydrogen ion Carbonate ion
or
H2CO3 (aq) ⇌ 2H+(aq) + CO32-(aq)
(iii) H3PO4 + water ⇌ 3H+(aq) + PO43-(aq)
phosphoric acid hydrogen ion phosphate ion
or
H3PO4 (aq) ⇌ 3H+(aq) + PO43-(aq)
(iv) HCOOH + water ⇌ HCOO⁻(aq) + H+(aq)
formic acid formate ion hydrogen ion
or
HCOOH(aq) ⇌ HCOO⁻(aq) + H+(aq)
Characteristics of weak acids:
Due to small amounts of H+ (aq) ions in the solutions of weak acids,
(i) They react quite slowly with other substances (such as metals, metal carbonates and metal bicarbonates etc).
(ii) They have low electrical conductivity.
(iii) They are weak electrolytes.
Conclusion:
Greater the degree of ionization, greater is the amount of H+ (aq) ions produced in solution and stronger is the acid (or greater is strength of acid).
Smaller the degree of ionization, smaller is the amount of H+ (aq) ions produced in the solution and weaker is the acid (or lesser is the strength of acid).
Thus, strength of an acid is directly proportional to the degree of ionization.
Dilution of Concentrated Acids an Exothermic Reaction
Concentrated acid:
Pure acid is generally known as the concentrated acid.
Dilute acid:
A concentrated acid mixed with water is called a dilute acid and this process of mixing of water to a concentrated acid is called dilution.
Note: The dilution of an acid with water is an exothermic reaction i.e. on mixing water to an acid, heat is produced.
Experiment to verify that dilution of a concentrated acid is exothermic
Take a small amount of water in a beaker. Note its temperature. Now put a few drops of conc. H2SO4 or conc. HNO3 acid into it and note the temperature of beaker again.
Observation:
There is rise in temperature in each case.
Thus dilution of conc. acid is an exothermic reaction and is accompanied by ionization of acid as follows:
Chemical reactions:
Reaction 1:
H2SO4(l) + 2H2O → 2H3O+(aq) + SO42-(aq) + Heat
sulphuric acid (conc) water hydronium ion sulphate ion released
Reaction 2:
HNO3(l) + H2O(l) → H3O+(aq) + NO3-(aq) + Heat
nitric acid (conc.) water hydronium ion nitrate ion released
Conclusion:
From the above experiment we lead to a conclusion that dilution of concentrated acid in water is an exothermic (or heat releasing) reaction.
How to dilute a concentrated acid?
Since dilution of a concentrated acid is highly exothermic reaction, the heat produced is so large that the solution may splash out or glass beaker may break in which dilution is carried out due to excessive heating. Hence to slow down the exothermic process, dilution of a concentrated acid is always done by adding acid into water and not water into acid as shown in figure.

Conclusion:
We should dilute an acid by mixing acid into water and not water into acid.
Effect of dilution on [H+] of an acid:
On dilution, the [H+] in the solution decreases and the solution become less acidic (or strength of acid decreases). This can be verified by the following experiment
Experiment to verify that strength of an acid decreases on dilution
Take about 5 ml of dilute HCl acid in test tube A. In another test tube B, take 5 ml of more diluted HCl (10 times more dilute than HCl in test tube A). Similarly take about 5 ml of more diluted HCl (10 times more dilute than HCl in test tube B) in test tube C.
Now add few pieces of zinc granules in each of the test tubes.

Observation:
There is evolution of hydrogen (H2) gas in each case. According to the reaction:
Zn + 2HCl → ZnCl2 + H2(g)
zinc hydrochloric acid zinc chloride hydrogen
It is observed that the rate of evolution of H2 gas is fastest in test tube A (having small dilution) and lowest in test tube C (having large dilution) and moderate in test tube B.
Conclusion:
From the above experiment we lead to a conclusion that on dilution, [H+] in solution decreases. Thus acidic strength of an acid decreases on dilution (since strength of an acid is due to the presence of [H+] in solution).
Important Note: Acidic strength of an acid is affected by two factors:
(i) Degree of ionization of an acid:
i.e. strength of an acid ∝ degree of ionization
Greater the degree of ionization, greater will be [H+] in the solution and thus greater will be the strength of an acid (or stronger will be an acid). Similarly, smaller the degree of ionization smaller will be [H+] in solution and thus lesser will be the strength of an acid (or weaker will be the acid).
(ii) Dilution of an acid:
Strength of an acid is inversely proportional to the dilution of an acid, greater the dilution of an acid, greater the dilution of an acid, lesser will be [H+] in the solution and thus lesser will be the strength of an acid (or weaker will be the acid)
i.e strength of an acid ∝ 1/(dilution of an acid)
Similarly smaller the dilution of an acid, greater will be [H+] in solution and thus greater will be the strength of an acid (or stronger will be the acid).
MORE ABOUT ACIDS:
(i) Some naturally occurring acids: A few naturally occurring sources of acids and the acids present in them are given in table below:
| S. No. | Natural source | Acid Present |
| 1. | Oranges, lemons | Citric acid |
| 2. | Apples | Malic acid |
| 3. | Tomatoes | Oxalic acid |
| 4. | Tamarind (Imli) | Tartaric acid |
| 5. | Sour milk or curd | Lactic acid |
| 6. | Vinegar | Acetic acid |
| 7. | Proteins | Amino acids |
(ii) Handling acidic food stuff in the household : In traditional kitchens, copper and brass vessels are used even today. Hence, if curd or other sour substances which are acidic in nature are kept in these vessels, they react to form toxic compounds(since acids react with metals) and make the food stuff unfit for consumption.
Therefore, to protect them from such a reaction, these vessels have to be coated with a thin layer of tin(kalai) from time to time.
USEFULNESS OF CERTAIN ACIDS:
(i) Hydrochloric acid (HCl) produced in the stomach kills the harmful bacteria that may enter into the stomach along with the food we eat.
(ii) Vinegar (acetic acid) is used in the pickling of food as a method of preservation of food.
Base
Substances with bitter taste and soapy touch are regarded as bases. Since many bases like sodium hydroxide and potassium hydroxide have corrosive action on the skin and can even harm the body, so according to the modern definition a base may be defined as a substance capable of releasing one or more OH- ions in aqueous solution.
Alkalies:
Some bases like sodium hydroxide and potassium hydroxide are water soluble. These are known as alkalies. Therefore water soluble bases are known as alkalies eg. KOH, NaOH. A list of a few typical bases along with their chemical formulae and uses is given below:
| Name | Commercial Name | Chemical Formula | Uses |
| Sodium hydroxide | Caustic Soda | NaOH | In manufacture of soap, paper, pulp, rayon, refining of petroleum etc. |
| Potassium hydroxide | Caustic Sba | KHO | In alkaline storage batteries, manufacture of soap, absorbing CO2 gas etc. |
| Calcium hydroxide | Slaked lime | Ca(OH)2 | In manufacture of bleaching powder softening of hard water etc. |
| Magnesium hydroxide | Milk of Magnesia | Mg(OH)2 | As an antacid to remove acidity from stomach |
| Aluminum hydroxide | – | Al(OH)3 | As foaming agent in fire extinguishers. |
| Ammonium hydroxide | – | NH4OH | In removing greases stains from cloths and in cleaning window panes. |
PHYSICAL PROPERTIES OF BASES
(i) Bitter taste: Almost all basic substances have a bitter taste.
(ii) Action on litmus solution: Bases turn red litmus solution into blue.
(iii) Action on methyl orange: Bases turn methyl orange into yellow.
(iv) Action on phenolphthalein: Bases turn phenolphthalein into pink.
(v) Conduction of electricity: Like acid, the aqueous solution of a base also conducts electricity.
CHEMICAL PROPERTIES OF BASES
REACTION OF BASES WITH METALS:
Metals like zinc, tin and aluminum react with strong alkalies like NaOH (caustic soda), KOH (caustic potash) to evolve hydrogen gas.
Zn(s) + 2NaOH(aq) → Na2ZnO2 (aq) + H2 (g)
Sodium zincate
Sn(s) + 2NaOH(aq) → Na2SnO2 (aq) + H2 (g)
Sodium stannite
2Al(s) + 2NaOH + 2H2O → 2NaAlO2 (aq) + 3H2 (g)
Sodium meta aluminate
Experiment: Take 2-3 pieces of zinc granules in a test tube and add about 2-3 ml of conc. NaOH solution in to it and warm the contents.
Observation: There is evolution of H2 gas which burns with a pop sound (on bringing a burning candle near the mouth of tube).
The reaction involved is:

REACTION OF BASES WITH ACIDS (NEUTRALIZATION REACTION)
When a base reacts with an acid then salt and water are formed
i.e. Base + Acid → Salt + Water
This reaction is called neutralization reaction, because when base and acid react with each other, they neutralize each other's effect (i.e. acid destroys the basic property of a base and a base destroys the acidic property of an acid)
(i) NaOH(aq) + HCl(aq)→ NaCl(aq) + H2O(l) sodium hydroxide hydrochloric acid sodium chloride water (base) (acid) (salt)
(ii) 2NaOH(aq) + H2SO4(aq) → Na2SO4(aq) + 2H2O(l) sodium hydroxide sulphuric acid sodium sulphate water (base) (acid) (salt)
Conclusion: Reaction of a base with an acid is a neutralization of an acid by base
REACTION OF BASE WITH NON-METAL OXIDE:
Bases react with non-metal oxide to form salt and water
i.e. Non-metal oxide + Base Salt + water
This reaction is similar to the neutralization reaction between acid and base to form salt and water. Thus, the reaction between bases and non-metal oxides is a kind of neutralization reaction and shows that non-metal oxides are acidic oxides.
Reaction of calcium hydroxide (lime water) with carbon dioxide.
Calcium hydroxide (lime water) is a base and carbon dioxide (CO2) is a non-metal oxide, so when they react with each other, salt and water are produced according to the reaction:
Ca(OH)2 (aq) + CO2(g) → CaCO3(g) + H2O(l)
calcium hydroxide carbondioxide calcium water (lime water) (non-metal oxide) carbonate (base) (salt)
2NaOH(aq) + CO2(g) → Na2 CO3(aq) + H2O(l)
Ca(OH)2 (s) + SO2(g) → CaSO3(aq) + H2O(l)
Conclusion: Reactions of bases with non-metal oxides are neutralization reactions which show the acidic nature of non-metal oxide.
CLASSIFICATION OF BASES ON THE BASIS OF DEGREE OF IONIZATION
The bases are classified into two categories on the basis of degree of ionization as follows:
(i) Strong bases
(ii) Weak bases
Strong base: A base contains one or more hydroxyl (OH) groups which it releases in aqueous solution upon ionisation. Bases which are almost completely ionised in water, are known as strong bases.
e.g. Sodium hydroxide (NaOH), potassium hydroxide (OH) groups which it releases in aqueous solution upon ionisation. Bases which are almost completely ionised in water, are known as strong bases.
NaOH(s) + Water → Na+(aq) + OH-(aq)
KOH(s) + Water → K+(aq) + OH-(aq)
Both NaOH and KOH are deliquescent in nature which means that they absorb moisture from air and get liquefied.
Weak bases:
Bases that are feebly ionised on dissolving in water and reduce a low concentration of hydroxyl ions are called weak bases.
eg. Ca(OH)2, NH4OH
(i) NH4OH + H2O ⇌ NH4+ (aq) + OH⁻(aq) Ammonium hydroxide Water Ammonium ion hydroxide ion
or
NH4OH (aq) ⇌ NH4+ (aq) + OH-(aq)
(ii) Ca(OH)2 + H2O ⇌ Ca2+(aq) + 2OH-(aq) calcium hydroxide Water calcium ion hydroxide ion (lime water)
or
Ca(OH)2(aq) ⇌ Ca2+(aq) + 2OH-(aq)
(iii) Mg(OH)2 + H2O ⇌ Mg2+(aq) + 2OH⁻(aq) magnesium hydroxide Water magnesium ion hydroxide ion
or
Mg(OH)2(aq) ⇌ Mg2+(aq) + 2OH-(aq)
Conclusion:
Greater the degree of ionization, greater is the amount of OH-(aq) ions produced in the solution and thus stronger is the base (or greater is the strength of base).
Smaller the degree of ionization, smaller is the amount ofOH- (aq) ions produced in the solution and thus weaker is the base (or lesser is the strength of base). Thus, strength of base is directly proportional to the degree of ionization.
Strength of base μ Degree of ionization.
Dilution of base: an exothermic reaction
Like acids, dilution of bases with water or mixing of bases with water is an exothermic process e.g. if we dissolve bases like NaOH, KOH in water, the solution is found to be hotter. This shows that dissolution of bases in water is an exothermic process.
Effect of dilution on strength of a base:
Like acids, on dilution of base with water, [OH-] in the solution decrease and thus, solution becomes less basic (or strength of base decrease)
Important Note: Basic strength of a base is affected by two factors:
(i) Degree of ionization of a base i.e. strength of base ∝ degree of ionization. Greater the degree of ionization, greater will be [OH-] in the solution and thus greater will be the strength of a base (or stronger will be a base).
Similarly, smaller the degree of ionization, smaller will be [OH-] in the solution and thus, lesser will be the strength of the base (or weaker will be the base).
(ii) Dilution of a base: Strength of a base ∝ 1/(dilution of a base). Greater the dilution of a base, lesser will be [OH-] in the solution and thus, lesser will be the strength of the base (or weaker will be the base).
Similarly, smaller the dilution of a base, greater will [OH-] in the solution and thus, greater will be the strength of the base (or stronger will be the base).
Comparison Between properties of acids and bases:
| Acids | Bases |
| 1. Sour in taste. | 1. Bitterness in taste. |
| 2. Change colours of indicators e.g. Litmus turns from blue to red, phenolphthalein remains colourless. | 2. Change colours of indicators e.g., litmus turns from red to blue, phenolphthalein turns from colourless to pink. |
| 3. Shows electrolytic conductivity in aqueous solution. | 3. Shows electrolytic conductivity in aqueous solutions. |
| 4. Acidic properties disappear when reacts with bases (Neutralisation). | 4. Basic properties disappear when reacts with acids (Neutralisation). |
| 5. Acids decompose carbonate salts. | 5. No decomposition of carbonate salts by bases. |
INDICATORS
Indicator indicates the nature of particular solution whether acidic, basic or neutral. Apart from this, indicator also represents the change in nature of the solution from acidic to basic and vice versa. Indicators are basically coloured organic substances extracted from different plants.
INDICATORS SHOWING DIFFERENT COLOURS IN ACIDIC AND BASIC MEDIUM
LITMUS SOLUTION:
Litmus solution is a purple coloured dye extracted from the lichen plant. It is very interesting to note that litmus solution (purple colour) itself is neither acidic nor basic. To use it as an indicator, it is made acidic or alkaline.
The alkaline form of litmus solution is blue in colour and called blue litmus solution.
The acidic form of litmus solution is red in colour and called red litmus solution.
Blue litmus solution (blue in colour): It is obtained by making the purple litmus extract alkaline. Thus, it is basic in nature and acts as an acid-indicator by giving a characteristic change in its colour in acids.
Red litmus solution (red in colour): It is obtained by making the purple litmus extract acidic. Thus it is acidic in nature and acts as a base-indicator by giving a characteristic change in its colour in bases.
Now questions arise:
(i) How do they (litmus solutions) act as acid –base indicators?
(ii) How do they change their colours in acids and bases?
(iii) How do they test whether the given substance is acidic or basic?
Experiment to test: Take about 2 - 4 ml of distilled water in two test tubes and add 1-2 drops of blue litmus solution in one test tube and red litmus in another test tube. Now add the sample solution of the substance to be tested in both test tubes (fig.)

Observation:
(i) Blue litmus solution turns red in acidic medium i.e. blue litmus solution changes into red if the sample solution (to be tested) is acidic.
(ii) Red litmus solution turns blue in basic medium i.e red litmus solution changes into blue
if the sample solution (to be tested) is basic.
The above observation can be shown more clearly by taking examples of some commonly used substance as follows.
Table 2
| Acidic substance turning blue litmus solution into red | Basic substance turning red litmus solution into blue |
|
Vinegar Lemon Juice Tamarind (imli) Sour milk or curd Proteins Tomatoes Apples Oranges Juice of unripe mangoes |
Baking soda solution Washing soda solution Bitter gourd (karela) extract Cucumber (kheera) extract |
It is clear from the above that blue litmus solution acts as acid indicator by giving red colour in acidic medium and red litmus solution acts as base indicator by giving blue colour in basic medium.
Thus litmus solution acts as an acid-base indicator.
TURMERIC (HALDI):
Turmeric used in kitchen can also be used to test a basic solution i.e. it act as base indicator by giving brown colour in basic medium. In other words yellow colour of haldi turns into brown in basic substances (due to base present in them) and thus distinguishes between acids and bases.
e.g. While eating food, if curry falls on the white clothes, a yellow stain is produced in the clothes. When we apply soap solution (basic in nature) on the cloth, the yellow stain becomes brown due to base present in soap solution.
This example shows that turmeric (haldi) act as base indicator by giving brown colour in basic substances.
SYNTHETIC INDICATORS:
The synthetic chemical substances which change their colour in acids and bases and thus distinguish between them are called synthetic indicators. Since they distinguish between acids and bases, so they are also called synthetic acid base indicators. The two most common synthetic indicators are
(a) Phenolphthalein and
(b) Methyl orange.
Now questions arise
(i) How do they (synthetic indicators) act as acid-base indicators?
(ii) How do they change their colour in acids and bases?
(iii) How do they test whether the given substance is acidic or basic?
Experiment to test: Take about 2 ml of sample solution (substance to be tested) in two test tubes and add 2-3 drops of phenolphthalein and methyl orange (synthetic acid-base indicators) to then as shown in figure.

Observation:
(a) Colour changes which take place in phenolphthalein are
(i) Phenolphthalein (whose natural colour is colourless) is colourless in acidic medium.
(ii) Phenolphthalein gives pink colour in basic medium or solution.
(b) Colour changes which take place in methyl orange are
(i) Methyl orange (whose natural colour is orange) gives pink colour in acidic medium or solution.
(ii) Methyl orange gives yellow colour in basic medium or solution.
The above observation can be shown clearly by taking examples of some commonly used substances as follows:
Table - 3
| Acidic substances turning methyl orange into pink and phenolphthalein remaining colourless | Basic substances turning methyl orange into yellow and phenolphthalein into pink |
|
Vinegar Lemon Juice Tamarind (imli) Sour milk or curd Proteins Tomatoes Oranges Juice of unripe mangoes |
Baking soda solution Washing soda solution Bitter gourd (karela) extract Cucumber (kheera) extract |
Now, if we see table 2 and table 3 observations, then we conclude that acid – base indicators like (litmus solution i.e. blue litmus solution and red litmus solution), phenolphthalein and methyl orange distinguishes between acids and bases by giving different colours (table 4)
Table – 4
| Sample solution | Red litmussolution | Blue litmussolution | Phenolphthalein indicator | Methyl orange indicator |
|
Vinegar |
No colour change |
Red |
Colourless |
Pink |
|
Lemon juice |
No colour change |
Red |
Colourless |
Pink |
|
Washing soda solution |
Blue |
No colour change |
Pink |
Yellow |
|
Baking soda solution |
Blue |
No colour change |
Pink |
Yellow |
|
Tamarind (imli) |
No colour change |
Red |
Colourless |
Pink |
|
Sour milk or curd |
No colour change |
Red |
Colourless |
Pink |
|
Proteins |
No colour change |
Red |
Colourless |
Pink |
|
Bitter gourd (karela) extract |
Blue |
No colour change |
Pink |
Yellow |
|
Oranges |
No colour change |
Red |
Colourless |
Pink |
|
Cucumber (kheera) Extract |
Blue |
No colour change |
Pink |
Yellow |
|
Tomatoes |
No colour change |
Red |
Colourless |
Pink |
|
Juice of unripe mangoes |
No colour change |
Red |
Colourless |
Pink |
The above observation can be shown more clearly as follows
Table – 5
| Indicator | Colour in acidic solution | Colour in basic solution |
|
Blue litmus solution Red litmus solution Phenolphthalein Methyl orange |
Red No colour change Colourless Pink |
No colour change Blue Pink Yellow |
It is clear from the above table that to test whether a substance is acidic or basic we can use any one of the above indicators. The change in colour with these indicators for the substance taken, shows its acidic or basic nature.
INDICATORS GIVING DIFFERENT ODOURS IN ACIDIC AND BASIC MEDIUM
(Olfactory Indicators)
There is another type of acid-base indicator which distinguishes between acids and base by giving different odour or smell in acidic and basic medium i.e. they give one type of odour or smell in acidic medium and a different odour or smell in basic medium and thus it can distinguish between acids and bases.
These indicators which give different odours or smells in acidic and basic medium are called olfactory indicators.
A few of these are given below:
(a) onion odoured cloth strip
(b) vanilla extract
(c) clove oil
Test with onion odoured cloth strip:
Take 1-2 ml of dil HCl in a test tube and add 1-2 ml of a basic solution like dil NaOH solution in another test tube. Add a small cloth strip treated with onion extract in each test tube and shake well.
Observation:
(i) acidic solution like dil HCl does not destroy the smell of onion.
(ii) basic solution like dil NaOH destroy the smell of onion.
Thus onion odoured cloth strip can be used as a test for acids and bases.
Test with vanilla extract:
Take 1-2 ml of acidic solution like dil HCl in one test tube and 1-2 ml of dil NaOH (basic solution) in another test tube. Add a few drops of vanilla extract (having characteristic pleasant smell) in each test tube and shake well.
Observation:
(i) Acidic solution like dil HCl does not destroy the characteristic smell of vanilla extract.
(ii) Basic solution like dilute NaOH destroy the smell of vanilla extract.
Thus vanilla extract can be used to test for acids and bases.
Test with clove oil:
Take about 1-2 ml of dil HCl in one test tube and 1-2 ml of dil NaOH in another test tube. Add a few drops of clove oil extract (having a characteristic smell or odour) in each test tube and shake well.
Observation:
(i) Acidic solution like dil HCl does not destroy the characteristic smell or odour of clove oil.
(ii) Basic solution like dil NaOH destroy the odour or smell of clove oil.
Thus clove oil can be used to test for acids and bases.
The above observations can be shown more clearly as follows:
Table - 6
|
Indicator |
Odour or smell in acidic solution |
Odour or smell in basic solution |
|
Onion Odoured cloth strip Clove oil Vanilla extract |
No change No change No change |
Cannot be detected Cannot be detected Cannot be detected |
It is clear from the above table that the olfactory indicators like clove oil, vanilla extract, onion odoured cloth strip, etc. can distinguish between acids and bases by giving different odours or smells in acidic and basic medium.
NEUTRALISATION:
It may be defined as a reaction between acid and base present in aqueous solution to form salt and water.
HCl (aq) + NaOH (aq) → NaCl (aq) + H2O (l)
Basically neutralisation is the combination between H+ ions of the acid with OH- ions of the base to form H2O.
For e.g. H+(aq) + Cl-(aq) + Na+(aq) + OH-(aq) → Na+(aq) + Cl-(aq) + H2O(l)
H+(aq) + OH-(aq) → H2O(l)
Neutralisation reaction involving an acid and base is of exothermic nature. Heat is evolved in all neutralisation reactions. If both acid and base are strong, the value of heat energy evolved remains same irrespective of their nature.
For e.g.
HCl(aq)+ NaOH(aq) → NaCl(aq) + H2O(l) + 57.1kJ Strong acid Strong Base
HNO3(aq)+ KOH(aq) → KNO3(aq) + H2O(l) + 57.1kJ Strong acid Strong Base
Strong acids and strong bases are completely ionised of their own in the solution, No energy is needed for their ionisation. Since the cation of base and anion of acid on both sides of the equation cancels out completely, the heat evolved is given by the following reaction
H+(aq) + OH-(aq) → H2O(l) + 57.1 kJ
Reaction of strong acid and strong base evolves 57.14 J.
APPLICATIONS OF NEUTRALISATION:
(i) People particularly of old age suffer from acidity problems in the stomach which is caused mainly due to release of excessive gastric juices containing HCI. The acidity is neutralised by antacid tablets which contain sodium hydrogen carbonate (baking soda), magnesium hydroxide etc.
(ii) The stings of bees and ants contain formic acid. Its corrosive and poisonous effect can be neutralised by rubbing soap which contains NaOH (an alkali).
(iii) The stings of wasps contain an alkali and its poisonous effect can be neutralised by an acid like acetic acid (present in vinegar).
(iv) Farmers generally neutralise the effect of acidity in the soil caused by acid rain by adding slaked lime (Calcium hydroxide) to the soil.
Strength of Acid and Base Solution: pH Scale
pH scale: A scale developing for measuring hydrogen ion concentration in a solution called pH scale, has been developed by S.P.L. sorrensen. The P in pH stands for 'potenz' in German power. On the pH scale we can measure pH from O (very acidic) to 14(very alkaline). pH should be thought of simply as a number which indicates the acidic or basic nature of solution. Higher the hydrogen ion concentration, Lower is the pH scale.
(i) For acidic solution, pH < 7
(ii) For alkaline solution, pH > 7
(iii) For neutral solution, pH = 7
Strength of Acid and Base Solution: pH Scale
pH scale: A scale developing for measuring hydrogen ion concentration in a solution called pH scale, has been developed by S.P.L. sorrensen. The P in pH stands for 'potenz' in German power. On the pH scale we can measure pH from O (very acidic) to 14(very alkaline). pH should be thought of simply as a number which indicates the acidic or basic nature of solution. Higher the hydrogen ion concentration, Lower is the pH scale.
(i) For acidic solution, pH < 7
(ii) For alkaline solution, pH > 7
(iii) For neutral solution, pH = 7

pH is defined as negative logarithm of [H+] or [H3O+]
i.e. pH = −log[H+] or pH = −log[H3O+]
e.g. if [H+] = 10-1 mol L-1, then pH = −log(10-1) = log10 = 1
if [H+] = 10-2 mol L-1, then pH = −log(10-2) = 2log10 = 2
It is clear from the above expression that pH of a solution is the magnitude of the negative power to which 10 must be raised to express the [H+] of the solution in mol L-1.
In other words, pH stands for power of hydrogen ions (p stands for power and H stands for hydrogen)
e.g.
If [H+] = 10⁻¹ mol L-1, then pH = 1
If [H+] = 10-2 mol L-1, then pH = 2
If [H+] = 10-6 mol L-1, then pH = 6 and so on
and If [OH-] = 10-6 mol L-1, then [H+] = 10-8 mol L-1 and pH = 8
[∵ [H+][OH-] = 10-14 mol L-1 at 298K ⇒ 10-6 × 10-8 = 10-14 mol L-1]
similarly if [OH⁻] = 10-14 mol L-1 then [H+] = 100 ∵[H+][OH-] = 10-14
so that [100 × 10⁻-14 = 10-14]
and pH = 0
if [OH-] = 100 mol L-1, [H⁺] = 10-14 [so that 10-14 × 100 = 10-14] and pH = 14 and so on
pH values for acidic or basic or neutral solution in terms of [H+] can be expressed as follows:
FOR A NEUTRAL SOLUTION (OR WATER)
[H⁺] = [OH⁻] = 10⁻⁷ mol L⁻¹
⇒ its pH = 7 (magnitude of negative power to which 10 must be raised to express [H⁺])
FOR AN ACIDIC SOLUTION
[H⁺] > [OH⁻]
or [H⁺] > 10⁻⁷ mol L⁻¹ (i.e. 10⁻⁶, 10⁻⁵, 10⁻⁴ etc.)
⇒ its pH < 7 (i.e. 6, 5, 4, ....0)
FOR A BASIC SOLUTION
[OH⁻] > [H⁺]
or [OH⁻] > 10⁻⁷ mol L⁻¹ (i.e. 10⁻⁶, 10⁻⁵, 10⁻⁴ etc.)
or [H⁺] < 10⁻⁷ mol L⁻¹ (i.e. 10⁻⁸, 10⁻⁹, 10⁻¹⁰ etc so that [H⁺][OH⁻] = 10⁻¹⁴)
⇒ its pH > 7 (i.e. 8, 9, 10, ....14)
Hence, acidic or basic strength or neutral nature of solution may be expressed on the pH scale from 0 to 14 as follows:

Conclusion: From the above figure, we lead to a conclusion that
(i) for a neutral solution, pH = 7
(ii) for a basic solution, pH > 7
(iii) for an acidic solution, pH < 7
Universal indicator papers for pH values:
Indicators like litmus, phenolphthalein and methyl orange are used in predicting the acidic and basic characters of the solutions. However universal indicator papers have been developed to predict the pH of different solutions. Such papers represent specific colours for different concentrations in terms of pH values.
The exact pH of the solution can be measured with the help of pH meter which gives instant reading and it can be relied upon.
pH values of a few common solutions are given below :
| Solution | Approximate pH | Solution |
Approximate pH |
|
Gastric Juices |
1.0 - 3.0 |
Pure water |
7.0 |
|
Lemon juices |
2.2-2.4 |
Blood |
7.36-7.42 |
|
Vinegar |
3.0 |
Baking soda solution |
8.4 |
|
Beer |
4.0-5.0 |
Sea water |
9.0 |
|
Tomato juice |
4.1 |
Washing soda solution |
10.5 |
|
Coffee |
4.5-5.5 |
Lime water |
12.0 |
|
Acid rain |
5.6 |
House hold ammonia |
11.9 |
|
Milk |
6.5 |
Sodium hydroxide |
14.0 |
|
Saliva |
6.5-7.5 |
(b) Significance of pH in daily life:
(i) pH in our digestive system: Dilute hydrochloric acid produced in our stomach helps in the digestion of food. However, excess of acid causes indigestion and leads to pain as well as irritation. The pH of the digestive system in the stomach will decrease. The excessive acid can be neutralised with the help of antacid which are recommended by the doctors. Actually, these are group of compounds (basic in nature) and have hardly any side effects. A very popular antacid is 'Milk of Magnesia' which is insoluble magnesium hydroxide. Aluminium hydroxide and sodium hydrogen carbonate can also be used for the same purpose. These antacids will bring the pH of the system back to its normal value. The pH of human blood varies from 7.36 to 7.42. It is maintained by the soluble bicarbonates and carbonic acid present in the blood. These are known as buffers.
(ii) pH change leads to tooth decay: The white enamel coating on our teeth is of insoluble calcium phosphate which is quite hard. It is not affected by water. However, when the pH in the mouth falls below 5.5 the enamel gets corroded. Water will have a direct access to the roots and decay of teeth will occur. The bacteria present in the mouth break down the sugar that we eat in one form or the other to acids; Lactic acid is one of these. The formation of these acids causes decrease in pH. It is therefore advisable to avoid eating sugary foods and also to keep the mouth clean so that sugar and food particles may not be present. The tooth pastes contain in them some basic ingredients and they help in neutralising the effect of the acids and also increasing the pH in the mouth.
(iii) Role of pH in curing stings by insects: The stings of bees and ants contain methanoic acid (or formic acid). When stung, they cause lot of pain and irritation. The cure is in rubbing the affected area with soap. Sodium hydroxide present in the soap neutralises acid injected in the body and thus brings the pH back to its original level bringing relief to the person who has been stung. Similarly, the effect of stings by wasps containing alkali is neutralised by the application of vinegar which is ethanoic acid (or acetic acid)
(iv) Soil pH and plant growth: The growth of plants in a particular soil is also related to its pH. Actually, different plants prefer different pH range for their growth. It is therefore, quite important to provide the soil with proper pH for their healthy growth. Soils with high iron minerals or with vegetation tend to become acidic. The soil pH can reach as low as 4.The acidic effect can be neutralised by 'liming the soil' which is carried by adding calcium hydroxide. These are all basic in nature and have neutralising effect. Similarly, the soil with excess of lime stone or chalk is usually alkaline. Sometimes, its pH reaches as high as 8.3 and is quite harmful for the plant growth. In order to reduce the alkaline effect, it is better to add some decaying organic matter (compost or manure). The soil pH is also affected by the acid rain and the use of fertilizers. Therefore soil treatment is quite essential.
SALTS
A substance formed by neutralization of an acid with a base is called a salt. For e.g.
Ca(OH)₂ + H₂SO₄ → CaSO₄ + H₂O
2Cu(OH)₂ + 4HNO₃ → 2Cu(NO₃)₂ + 2H₂O
NaOH + HCl → NaCl + H₂O
CLASSIFICATION OF SALTS:
Salts have been classified on the basis of chemical formulae as well as pH values.
(a) Classification Based on Chemical Formulae
(i) Normal salts: A normal salt is the one which does not contain any ionisable hydrogen atom or hydroxyl group. This means that it has been formed by the complete neutralisation of an acid by a base.
For e.g. NaCl, KCl, NaNO₃, K₂SO₄ etc.
(ii) Acidic salts: An acidic salt is that which contains some replaceable hydrogen atoms. This means that the neutralisation of acid by the base is not complete. For example, sodium hydrogen sulphate (NaHSO₄), sodium hydrogen carbonate (NaHCO₃) etc.
(iii) Basic salts: A basic salt is that which contains some replaceable hydroxyl groups. This means that the neutralisation of base by the acid is not complete. For example, basic lead nitrate Pb(OH)NO₃, Basic lead chloride, Pb(OH)Cl etc.
(b) Classification Based on pH Values:
Salts are formed by the reaction between acids and bases. Depending upon the ^nature of the acids and bases or upon the pH values, the salt solutions are of three types.
(i) Neutral salt solutions: Salt solutions of strong acids and strong bases are neutral and have pH equal to 7. They do not change the colour of litmus solution.
For e.g.: NaCl, KCl, NaNO₃, Na₂SO₄ etc.
(ii) Acidic salt solutions: Salt solutions of strong acids and weak bases are of acidic nature and have pH less than 7. They change the colour of blue litmus to red. For e.g. (NH₄)₂SO₄, NH₄Cl etc. In both these salts, the base NH₄OH is weak while the acids H₂SO₄ and HCl are strong.
(iii) Basic salt solutions: Salt solutions of strong bases and weak acids are of basic nature and have pH more than 7. They change the colour of red litmus solution to blue. For e.g. Na2CO3, K3PO4 etc.
In both the salts, bases NaOH and KOH are strong while the acids H2CO3 and H3PO4 are weak.
Uses of Salt
(i) As a table salt.
(ii) In the manufacture of butter and cheese.
(iii) In the manufacturing of washing soda and baking soda.
(iv) For the preparation of sodium hydroxide by electrolysis of brine.
(v) Rock salt is spread on ice to melt it in cold countries.
Some Important Chemical Compounds
Sodium Chloride - Common salt (table salt):
Sodium chloride (NaCI) also called common salt or table salt is the most essential part of our diet. Chemically it is formed by the reaction between solutions of sodium hydroxide and hydrochloric acid. Sea water is the major source of sodium chloride where it is present in dissolved form along with other soluble salts such as chlorides and sulphates of calcium and magnesium; It is separated by some suitable methods. Deposits of the salts are found in different parts of the world and are known as rock salt. When pure, it is a white crystalline solid, However, it is often brown due to the presence of impurities.
Occurrence and extraction of common salt:
The common salt occurs naturally in sea water, in land lakes and in rock salt. The extraction of common salt from these sources are given below:
(i) Common salt from sea water
Sea water contains many dissolved salts in it. The major salt present in sea water is common salt (or NaCl). The common salt is obtained from sea water by the process of evaporation which is done as follows:
Sea water is trapped in large shallow pools and allowed to stand there. The sun’s heat evaporates the water slowly and common salt is left behind. This salt contains impurities of MgCl2, MgSO4 etc and thus purified by removing these impurities by suitable method before it is sold in the market.
(ii) Common salt from inland lakes
Large quantities of salt are obtained by natural evaporation of water of inland lakes e.g. Sambhar lake in Rajasthan (India), Great salt lake (Utah, USA) and Lake Elton (Russia).
(iii) Common salt from underground deposits
The large crystals of common salt found in underground ellipsoids is called “Rock salt”. It is usually brown due to presence of impurities in it. Rock salt is mined from underground deposits just like coal.
Common salt is an important starting material for the production of a number of other chemicals such as
- Sodium hydroxide (caustic soda).
- Calcium oxychloride (bleaching powder).
- Sodium carbonate (washing soda) .
- Sodium hydrogen carbonate (baking soda) and many others.
Uses:
(i) Essential for life: Sodium chloride is quite essential for life. Biologically, it has a number of functions to perform such as in muscle contraction, in conduction of nerve impulse in the nervous system and is also converted in hydrochloric acid which helps in the digestion of food in the stomach. When we sweat, there is loss of sodium chloride along with water. It leads to muscle cramps. Its loss has to be compensated suitably by giving certain salt preparations to the patient. Electrol powder is an important substitute of common salt.
(ii) Raw material for chemicals: Sodium chloride is also a very useful raw material for different chemicals. A few out of these are hydrochloric acid (HCl), washing soda (Na2CO3.10H2O), baking soda (NaHCO3) etc. Upon electrolysis of a strong solution of the salt (brine), sodium hydroxide, chlorine and hydrogen are obtained. Apart from these, it is used in leather industry for the leather tanning. In severe cold, rock salt is spread on icy roads to melt ice. It is also used as a fertilizer for sugar beet.
Electrolysis of aqueous solution of NaCl:
2NaCl(s) + 2H₂O(l) - electrolysis → 2NaOH(aq) + Cl₂(g) + H₂(g)
reaction takes place in two steps
(i) 2Cl⁻ → Cl₂(g) + 2e⁻ (anode reaction)
(ii) 2H₂O + 2e⁻ → H₂ + OH⁻ (cathode reaction)
WASHING SODA: (Na₂CO₃.10H₂O)
Chemical name: Sodium carbonate decahydrate
Chemical formula: Na₂CO₃. 10H₂O
Sodium carbonate is recrystallised by dissolving in water to get washing soda it is a basic salt.
Na₂CO₃ + 10H₂O → Na₂CO₃.10H₂O
(Sodium (Washing soda) Carbonate)
(i) Manufacture of washing soda
Washing soda is manufactured from sodium chloride (or common salt) in the following three steps:
Manufacture of sodium hydrogen carbonate (baking soda) by solvay process: A cold and concentrated solution of sodium chloride (brine) is reacted with ammonia and CO₂ to obtain sodium hydrogen carbonate
NaCl + H₂O + NH₃ + CO₂ → NaHCO₃ + NH₄Cl
sodium water ammonia carbondioxide sodium ammonium chloride chloride bicarbonate
Thermal decomposition of sodium hydrogen carbonate (or baking soda): On heating sodium hydrogen carbonate decomposes to form sodium carbonate.
2NaHCO₃ — heat → Na₂CO₃(s) + CO₂(l) + H₂O(g)
sod. hydrogen sod. carbonate carbon dioxide water carbonate (Anhydrous)
Re-crystallization of sodium carbonate (or soda ash):
Anhydrous sodium carbonate (or soda ash) obtained in step 2 is dissolved in water and subjected to re-crystallization. As a result, crystals of washing soda (sodium carbonate decahydrate) are obtained.
Na₂CO₃(s) + 10H₂O(l) → Na₂CO₃.10H₂O(s)
soda ash water washing soda
(ii) Properties of Washing Soda
(a) Colour and state: It is a transparent crystalline solid (when freshly prepared) containing 10 molecules of water of crystallisation.
(b) Action of air: On exposure to air, washing soda crystals lose 9 molecules of water of crystallisation to form a monohydrate which is a white powder
Na₂CO₃.10H₂O(s) - Exposed to air → Na₂CO₃.H₂O + 9H₂O
(transparent crystals)
This process is called efflorescence
(c) Action of heat: On heating, washing soda loses all the molecule of water and becomes anhydrous.
Na₂CO₃.10H₂O - Heat → Na₂CO₃ + 10H₂O
Hydrated washing soda Anhydrous sodium water carbonate (soda ash)
Uses:
(i) It is used as cleansing agent for domestic purposes.
(ii) It is used in softening hard water and controlling the pH of water.
(iii) It is used in manufacture of glass.
(iv) Due to its detergent properties, it is used as a constituent of several dry soap powders.
(v) It also finds use in photography, textile and paper industries etc.
(vi) It is used in the manufacture of borax (Na₂B₄O₇.10H₂O).
BAKING SODA (NaHCO₃)
Baking soda is sodium hydrogen carbonate or sodium bicarbonate (NaHCO₃).
(i) Manufacture of baking soda
(a) On large scale: Baking soda is produced on a large scale by reacting a cold and concentrated solution of sodium chloride (called brine) with ammonia and carbon dioxide.
NaCl + H₂O + NH₃ + CO₂ → NaHCO₃ + NH₄Cl
sodium chloride water ammonia carbon dioxide Baking soda ammonium chloride
This process is called solvay process.
(b) On small scale: On a small scale baking soda can be prepared in the laboratory by passing CO₂ gas through aqueous sodium carbonate solution.
Na₂CO₃ + H₂O + CO₂ → 2NaHCO₃
sodium carbonate water carbon dioxide baking soda
OR
Na₂CO₃(aq) + CO₂ → 2NaHCO₃
(ii) Properties of Baking soda
(a) Colour and state
It is a white crystalline solid.
(b) Alkaline nature
It is mild, non-corrosive base. The alkaline nature of baking soda is due to salt hydrolysis.
NaHCO₃ + H₂O → (hydrolysis) Na⁺(aq) + HCO₃⁻(aq)
baking soda water strong base weak acid
(sodium hydrogen carbonate)
HCO₃⁻ + H₂O ⇌ H₂CO₃ + OH⁻
Thus, salt solution is basic due to hydrolysis of HCO₃⁻ ions
(c) Action of heat
When solid baking soda (or its solution) is heated it decomposes to give sodium carbonate with the evolution of CO₂ gas.
2NaHCO₃ → (Heat) Na₂CO₃ + H₂O + CO₂
baking soda soda carbonate water carbon dioxide gas
The above reaction takes places when baking soda is heated during the cooking of food. Since baking soda gives CO₂ on heating, it is used as a constituent of baking powder.
Uses:
(i) It is used in the manufacture of baking powder. Baking powder is a mixture of potassium hydrogen tartarate and sodium bicarbonate. During the preparation of bread the evolution of carbon dioxide causes bread to rise (swell).
CH(OH)COOK CH(OH)COOK + NaHCO₃ → +CO₂ + H₂O CH(OH)COOH CH(OH)COONa
(ii) It is largely used in the treatment of acid spillage and in medicine as soda bicarb, which acts as an antacid.
(iii) It is an important chemical in the textile, tanning, paper and ceramic industries.
(iv) It is also used in a particular type of fire extinguishers. The following diagram shows a fire extinguisher that uses NaHCO₃ and H₂SO₄ to produce CO₂ gas. The extinguisher consists of a conical metallic container (a) with a nozzle (Z) at one end. A strong solution of NaHCO₃ is kept in the container. A glass ampoule (P) containing H₂SO₄ is attached to a knob (K) and placed inside the NaHCO₃ solution. The ampoule can be broken by hitting the knob. As soon as the acid comes in contact with the NaHCO₃ solution, CO₃ gas is formed. When enough pressure in built up inside the container, CO₂ gas rushes out through the nozzle (Z). Since CO₂ does not support combustion, a small fire can be put out by pointing the nozzle towards the fire. The gas is produced according to the following reaction.
2NaHCO₃ (aq) + H₂SO₄(aq) → Na₂SO₄ (aq) + 2H₂O(l) + 2CO₂(g)
BLEACHING POWDER (CaOCl₂.4H₂O, CaCl₂.(OH)₂. H₂O)
Bleaching powder is commercially called 'chloride of lime' or 'chlorinated lime'. It is principally calcium oxychloride having the following formula:
Cl - Ca - OCl
Bleaching powder is prepared by passing chlorine over slaked lime at 313 K.
Ca(OH)₂ (aq) + Cl₂ (g) - 313K → Ca(OCl)Cl(s) + H₂O (g)
Slaked lime Bleaching powder
Note: Bleaching powder is not a compound but a mixture of compounds: CaOCl₂.4H₂O, CaCl₂.Ca(OH)₂.H₂0
(i) Manufacture of bleaching powder
The bleaching powder is manufactured by the action of chlorine gas (produced as a bi-product during manufacture of caustic soda) on dry slaked lime Ca(OH)₂. The reactions involved are:
2NaCl(aq) + 2H₂O(l) electrolysis → 2NaOH(aq) + Cl₂(aq) + H₂
Ca(OH)₂ + Cl₂ → CaOCl₂ + H₂O
Slaked lime chlorine bleaching powder water
Uses:
(i) It is commonly used as a bleaching agent in paper and textile industries.
(ii) It is also used for disinfecting water to make water free from germs.
(iii) It is used to prepare chloroform.
(iv) It is also used to make wool shrink-proof.
Sodium hydroxide NaOH (caustic soda)
Sodium hydroxide is commonly known as caustic soda having chemical formula NaOH. It is a strong base.
(i) Manufacture of sodium hydroxide (NaOH)
Sodium hydroxide is manufactured by the electrolysis of a concentrated aqueous solution of sodium chloride (called brine) i.e., when electricity is passed through a concentrated aqueous solution of sodium chloride (called brine), it decomposes to form sodium hydroxide, chlorine and hydrogen.
2NaCl(aq) + 2H₂O(l) -Electrolysis → 2NaOH(aq) + Cl₂(g) + H₂(g)
sodium chloride water sodium hydroxide chlorine hydrogen (brine) (caustic soda)
This process is called correct-alkali process because of products formed: chlor for chlorine and alkali for sodium hydroxide.
During electrolysis, Cl₂ gas is produced at the anode (positive electrode), H₂ gas is produced at the cathode (negative electrode) and NaOH solution is produced near the cathode. These products i.e. NaOH, Cl₂(g) & H₂(g) obtained by chlor-alkali process have a large number of uses described below one by one.
(ii) Uses of sodium hydroxide (NaOH)
Sodium hydroxide (NaOH) is used
(a) For making soaps and detergents.
(b) For making artificial textile fibres.
(c) For making paper.
(d) In de-greasing metals.
(e) As reagent in laboratory.
(f) In absorbing poisonous gases.
(g) In petroleum industry.
(iii) Uses of chlorine (Cl2)
(a) As disinfectant and germicide for sterilization of drinking water and water in swimming pools.
(b) In manufacture of chlorofluorocarbons used as refrigerants.
(c) In manufacture of PVC (polyvinyl chloride) used for making shoe soles.
(d) In bleaching of wood pulp and cotton fibres.
(e) In manufacture of pesticides.
(iv) Uses of hydrogen (H2)
(i) To make ammonia for fertilizers.
(ii) In metallurgy to reduce heavy metal oxide to metals.
(iii) In hydrogenation of vegetable oils to form solid fats.
(iv) Liquid hydrogen is used as a fuel for rockets.
Hydrogen and chlorine (two products of chlor-alkali process), combine to produce another important chemical called hydrochloric acid (HCl).
So we will now give some of the uses of HCl.
(v) Uses of hydrochloric acid (HCl)
(i) For cleaning steel.
(ii) In the preparation of ammonium chloride.
(iii) In medicines and cosmetics.
(iv) In making plastics like PVC.
(v) As a reagent in the laboratory.
(vi) In making aqua regia (after mixing with HNO3) for dissolving gold and platinum. The uses of NaOH, Cl2, can be shown more clearly in the figure.
Note: Aqua-Regia is three parts conc. HCl and 1 part conc. HNO3 i.e. in Aqua-Regia HCl and HNO3 are present in 3 : 1 ratio.

ARE THE CRYSTALLINE SALTS REALLY DRY
The crystalline salts or crystals of salts appear to be dry but actually they are not. They contain water of crystallization. It can be explained as follows:
Water of crystallization: The fixed number of water molecules present in one formula unit of salt is called water of crystallization.
For example
(i) Sodium carbonate crystals (washing soda crystals) contains 10 molecules of water of crystallization in one formula unit and hence written as Na2CO3.10H2O .
(ii) Calcium sulphate crystals (gypsum crystals) contain 2 molecules of water of crystallization in one formula unit and hence written as CaSO4.2H2O.
(iii) Copper sulphate crystals contain 5 molecules of water of crystallization in one formula unit and hence written asCaSO4.5H2O.
It is clear from the above examples that water of crystallization is not free water, so it does not wet the salts. Thus the crystalline salts which seem to be dry contain water of crystallization. It can be explained more clearly by following experiment.
Experiment to test the presence of water of crystallization in a crystalline salt.
Take a few crystals of copper sulphate (CaSO4.5H2O) in a dry test tube. Copper sulphate crystals are blue in colour. Heat the test tube.
Observation:
(i) Blue copper sulphate crystals turn white.
(ii) Water vapours appear on the upper parts inside the test tube.

Explanation: The blue copper sulphate crystals (CuSO₄.5H₂O) on heating gives out water vapours which condensed on the upper parts of the test tube and the salt left behind was anhydrous copper sulphate (CuSO₄) which was white in colour.
Chemical Equation:
CuSO₄.5H₂O - heat → CuSO₄ + 5H₂O
Copper sulphate crystals (blue, hydrated) → copper sulphate (white, anhydrous) + 5H₂O
Conclusion: Crystalline salts contain water of crystallization which are lost on heating.
Types of salts on the basis of water of crystallization
Salts are classified into two types on the basis of water of crystallization
(i) Anhydrous salts: The salts which contain no water of crystallization e.g. NaCl, CuSO₄.
(ii) Hydrated salts: The salts which contain a fixed number of water molecules of crystallisation. A few examples of these salts are
(a) Copper sulphate (CuSO₄.5H₂O).
(b) Washing soda (Na₂CO₃.10H₂O).
(c) Gypsum (CaSO₄.2H₂O).
(d) Plaster of paris (CaSO₄.½H₂O).
Out of these plaster of paris is very useful salt which is discussed below:
PLASTER OF PARIS(CaSO₄·½H₂O)
(a) Preparation:
It is prepared by heating gypsum (CaSO₄·2H₂O) at about 373 K in large steel pots with mechanical stirrer, or in a revolving furnace.
2(CaSO₄·2H₂O) - 373K → (CaSO₄)₂·H₂O + 3H₂O Gypsum Plaster of Paris
or
(CaSO₄·2H₂O) → CaSO₄·½ H₂O + 3/2 H₂O Plaster of Paris
(Calcium sulphate hemihydrate)
The temperature is carefully controlled, as at higher temperature gypsum is fully dehydrated. The properties of dehydrated gypsum are completely different from those of Plaster of Paris
Properties of plaster of Paris (POP)
(a) Colour and state: It is a white powder.
(b) Reaction with water: Setting of Plaster of Paris (or POP).
When POP is mixed with water and left for half an hour to one hour, it sets to a hard mass due to rehydration of POP to gypsum.
CaSO₄. ½H₂O + 3/2 H₂O → CaSO₄.2H₂O
P.O.P. water gypsum
(c) Effect of heat: When POP is heated at 473K, it forms anhydrous calcium sulphate (CaSO₄) which is known as dead burnt plaster. It has no setting property as it takes up water very slowly.
CaSO₄ ½ H₂O 473 K → CaSO₄ + ½ H₂O
(P.O.P.) dead burnt plaster
(e) Uses:
When finely powdered Plaster of Paris is mixed with water and made into a paste, it quickly sets into a hard mass. In the process, its volume also increases slightly. These properties find a number of uses. Addition of water turns Plaster of Paris back into gypsum.
(i) It is used in the laboratories for sealing gaps where airtight arrangement is required.
(ii) It is also used for making toys, cosmetics and casts of statues.
(iii) It is used as a cast for setting broken bones.
(iv) It also finds use in making moulds in pottery.
(v) It is also used for making surfaces smooth and for making designs on walls and ceilings.
Ex.: Name the acid-base indicator extracted from Lichen.
Sol. Litmus.
Ex.: What colour do the following indicators turn to when added to an acid?
(a) Litmus
(b) Phenolphthalein
(c) Methyl orange
Sol. (a) Blue Litmus to red (b) colourless (c) Pink
Ex.: Name the acids present in
(i) Vinegar
(ii) Orange
Sol. (i) Acetic acid (ii) Citric acid
Ex.: A solution reacts with crushed egg-shell to give a gas that turns lime water milky. The solution contains:
(a) NaCl
(b) HCl
(c) LiCl
(d) KCl
Sol. (b) HCl
Ex.: What is an indicator? Name any two indicator.
Sol. An indicator is a ‘dye’ that changes the colour or odour when it is put in an acid or a base. An indicator helps us to know whether the given substance is acidic or basic in nature. The two common acid-base indicators are: Litmus and Methyl orange.
Ex.: Explain why, while diluting an acid, the acid should be added to water and not water to the acid.
Sol. We know that dilution of concentrated acid is a highly exothermic process. If water is added to concentrated acid, the heat produced is so large that the solution may splash out and it may even break the beaker in which the dilution is carried out. Hence, while diluting a concentrated acid; acid should be added to water and not vice-versa.
Ex.: You have been provided with three test-tubes. One of them contains distilled water and the other two contain an acidic solution and a basic solution, respectively. If you are given only red litmus paper, how will you identify the contents of each test-tube?
Sol. (a) Put the red litmus paper in all the test-tubes, turn by turn. The solution which turns red litmus paper to blue, will be a basic solution.
(b) Now put the blue litmus paper (obtained above) in the remaining two test-tubes, one by one. The solution which turns blue litmus paper to red, will be the acidic solution.
(c) The third test tube is distilled water.
Ex.: Name the substance which on treatment with chlorine yields bleaching powder.
Sol. Slaked lime, Ca(OH)2
Ex.: In addition to sodium hydrogen carbonate (NaHCO3) baking powder contains a substance X. Name the substance X.
Sol. Tartaric Acid.
Ex.: What happens when blue crystals of CuSO4 are heated?
Sol. When blue crystals of copper sulphate are heated, the water of crystallization is removed and anhydrous copper sulphate is formed which is white in colour.
Ex.: What does the pH of a solution signify? Explain your answer.
Sol. The pH of a solution signifies the acidic or basic nature of the solution. As we know that for an acidic solution pH < 7, for a basic solution pH > 7 and for a neutral solution pH = 7.
Ex.: Fresh milk has a pH of 6. How do you think the pH will change as it turns into curd? Explain your answer.
Sol. As the milk turns into curd, an acid known as lactic acid is produced and because of this the pH will decrease.
Ex.: What is a universal indicator? For what purpose it is used?
Sol. The universal indicator is a mixture of many different indicators (or dyes) which give different colour at different pH values of the substances (i.e. from 0 to 14). It is used to find
(i) Whether a given substance is acidic or basic in nature and
(ii) The strength of acid or base.
Ex.:Explain why plaster of paris should be stored in a moisture proof container?
Sol. Plaster of paris should be stored in a moisture proof container because in presence of moisture it gets hydrated. This will make it useless after some time as it losses its setting property.
Frequently Asked Questions
The fundamental difference between strong and weak acids lies in their degree of ionization when dissolved in water. Strong acids undergo complete ionization, meaning nearly all their molecules dissociate into hydrogen ions (H⁺) and corresponding anions. Common examples include hydrochloric acid (HCl), sulfuric acid (H₂SO₄), and nitric acid (HNO₃). When you dissolve HCl in water, virtually every HCl molecule separates into H⁺ and Cl⁻ ions, resulting in a high concentration of hydrogen ions in the solution.
Weak acids, conversely, only partially ionize in aqueous solutions. Acetic acid (CH₃COOH), found in vinegar, and carbonic acid (H₂CO₃), present in carbonated beverages, are typical weak acids. When acetic acid dissolves in water, only a small percentage of molecules release hydrogen ions, while most remain as intact CH₃COOH molecules. This equilibrium between ionized and non-ionized forms is represented by a double arrow in chemical equations, indicating the reversible nature of the reaction.
The practical implications of this difference are significant. Strong acids react more vigorously with metals, metal carbonates, and bases, producing reactions that occur rapidly and release considerable heat. They also have lower pH values—typically between 0 and 3 for concentrated solutions. Weak acids react more slowly and generate less heat during neutralization. Their pH values generally range from 3 to 6, depending on concentration.
From a safety perspective, strong acids pose greater corrosive hazards and require more careful handling. In industrial applications, strong acids are preferred when rapid, complete reactions are necessary, such as in metal processing or manufacturing certain chemicals. Weak acids find use in food preservation, as cleaning agents, and in biological systems where gentler acidic conditions are required. Understanding this distinction helps in selecting the appropriate acid for specific applications and implementing proper safety protocols.
This safety rule stems from the highly exothermic nature of acid dilution the process releases substantial heat energy. When concentrated acid mixes with water, the heat of hydration (energy released when water molecules surround and interact with ions) can be intense enough to cause dangerous consequences if not properly managed.
Adding water to concentrated acid creates an extremely hazardous situation. The small amount of water added initially has insufficient thermal mass to absorb and dissipate the large amount of heat generated. This causes the water to heat rapidly, potentially reaching boiling point almost instantly. The violent boiling produces spattering and splashing of concentrated acid, which can cause severe chemical burns to skin, eyes, and respiratory passages. In extreme cases, the glass container may crack or shatter from thermal shock, spreading corrosive liquid across the work area.
When acid is added to water—the correct procedure the situation reverses favorably. The larger volume of water acts as a heat sink, absorbing and distributing the thermal energy generated by dilution. Adding acid slowly, with constant stirring, ensures gradual mixing that prevents localized temperature spikes. The temperature rise remains manageable and controlled, typically warming the solution rather than causing boiling or violent reactions.
Consider sulfuric acid dilution specifically: concentrated H₂SO₄ (98%) mixed with water releases approximately 880 kJ per mole—enough energy to raise the temperature dramatically. Professional chemistry laboratories and industrial facilities maintain strict protocols requiring this "acid to water" approach. Additional safety measures include using heat-resistant glassware, working in well-ventilated fume hoods, wearing appropriate personal protective equipment (goggles, acid-resistant gloves, lab coats), and having neutralizing agents readily available.
This principle extends to other exothermic mixing processes in chemistry and serves as a fundamental safety practice that prevents countless accidents annually. Teaching this concept early in chemistry education establishes habits that protect students and professionals throughout their careers working with hazardous chemicals.
The pH scale represents a mathematical method for expressing hydrogen ion concentration in solutions, ranging from 0 to 14. Developed by Danish chemist S.P.L. Sorensen in 1909, "pH" stands for "power of hydrogen," derived from the German word "potenz." The scale's logarithmic nature provides a compact, practical way to represent the enormous range of hydrogen ion concentrations encountered in chemistry and biology.
Mathematically, pH equals the negative logarithm (base 10) of the hydrogen ion concentration: pH = -log[H⁺]. This logarithmic relationship means each unit change in pH represents a tenfold change in hydrogen ion concentration. A solution with pH 3 contains ten times more H⁺ ions than one with pH 4, and 100 times more than pH 5. This exponential relationship explains why small pH changes can have dramatic effects on chemical reactions and biological systems.
Pure water at 25°C has equal concentrations of H⁺ and OH⁻ ions, both at 10⁻⁷ mol/L, resulting in pH 7—the neutral point. Acidic solutions contain higher H⁺ concentrations than OH⁻, yielding pH values below 7. Basic solutions have lower H⁺ concentrations (higher OH⁻), producing pH values above 7. The relationship [H⁺][OH⁻] = 10⁻¹⁴ always holds at standard temperature, meaning as one increases, the other decreases reciprocally.
The logarithmic scale compresses a vast concentration range into manageable numbers. Without it, we would express hydrogen ion concentrations as cumbersome decimal numbers like 0.0000001 mol/L. Instead, we simply say pH 7. This practical advantage makes the pH scale universally adopted across scientific disciplines, medicine, environmental science, and industrial applications.
Precise pH measurement requires either electronic pH meters (using glass electrodes sensitive to H⁺ concentration) or universal indicator solutions that display different colors across the pH range. These tools allow monitoring of everything from blood chemistry (pH 7.35-7.45) to soil acidity for agriculture to swimming pool maintenance, demonstrating the scale's versatility and importance in diverse fields.
Neutralization represents the chemical reaction between an acid and a base that produces salt and water. At the molecular level, this process involves hydrogen ions (H⁺) from the acid combining with hydroxide ions (OH⁻) from the base to form water molecules (H₂O). The remaining ions—the cation from the base and the anion from the acid combine to form an ionic compound called a salt. The general equation is: Acid + Base → Salt + Water.
When hydrochloric acid reacts with sodium hydroxide, for example, H⁺ ions from HCl combine with OH⁻ ions from NaOH to create water, while Na⁺ and Cl⁻ ions remain in solution as sodium chloride (common table salt): HCl + NaOH → NaCl + H₂O. This reaction is highly exothermic, releasing approximately 57.1 kilojoules of energy per mole when strong acids react with strong bases, as the formation of water from ions represents a thermodynamically favorable process.
The importance of neutralization extends across numerous practical applications. In medicine, antacids containing basic compounds like magnesium hydroxide or sodium hydrogen carbonate neutralize excess hydrochloric acid in the stomach, relieving symptoms of acid indigestion and heartburn. Without this neutralization, excess stomach acid causes pain and potentially damages the esophageal and gastric linings.
Environmental applications include treating acidic industrial wastewater before discharge, where bases like calcium hydroxide neutralize harmful acids, protecting aquatic ecosystems. Agricultural lime (calcium hydroxide) neutralizes acidic soils affected by acid rain, restoring optimal pH for crop growth. In first aid, neutralization provides immediate treatment for chemical burns—weak bases for acid spills, weak acids for base exposures.
In analytical chemistry, neutralization forms the basis for titration, a quantitative technique determining unknown acid or base concentrations with remarkable precision. Industrial processes from soap manufacturing to pharmaceutical production rely on controlled neutralization reactions. Understanding neutralization mechanisms allows chemists to predict reaction outcomes, calculate exact quantities needed for complete reactions, and design processes that efficiently convert acids and bases into useful products while managing heat generation safely.
Water of crystallization refers to water molecules incorporated into the crystal structure of certain salts in fixed, stoichiometric ratios. These water molecules are not merely adsorbed moisture on the crystal surface but are chemically bound within the crystalline lattice, forming an integral part of the compound's structure. The presence and number of these water molecules significantly affect the salt's physical properties, appearance, and behavior.
Copper sulfate provides an excellent example: the hydrated form (CuSO₄·5H₂O) appears as blue crystals, with five water molecules per formula unit. When heated, these water molecules are driven off, leaving anhydrous copper sulfate (CuSO₄), which is white. This dramatic color change demonstrates how water of crystallization affects physical properties. The dot notation (·5H₂O) indicates these water molecules are distinct from the main ionic compound yet structurally incorporated. When anhydrous copper sulfate reabsorbs water from the atmosphere, it reconverts to the blue hydrated form, releasing heat in the process—a property exploited in some moisture detection applications.
Washing soda (sodium carbonate decahydrate, Na₂CO₃·10H₂O) contains ten water molecules of crystallization. Fresh crystals appear transparent but gradually lose nine water molecules when exposed to air through a process called efflorescence, forming the monohydrate (Na₂CO₃·H₂O) as a white powder. This demonstrates how water of crystallization can be lost spontaneously under certain environmental conditions.
Gypsum (CaSO₄·2H₂O) and its relationship with Plaster of Paris (CaSO₄·½H₂O) illustrates practical applications. Heating gypsum to 373 K removes 1.5 water molecules per formula unit, producing Plaster of Paris. When water is added back, Plaster of Paris rehydrates to gypsum, expanding slightly and hardening—the principle behind its use in medical casts, sculpture molds, and construction applications. The "half" water molecule in Plaster of Paris's formula represents one water molecule shared between two formula units in the crystal structure.
Understanding water of crystallization is essential for accurate chemical calculations, proper storage of hydrated salts, and predicting how compounds behave under different conditions. Pharmacists must account for water of crystallization when preparing medications to ensure correct dosages. Industrial chemists consider it when calculating raw material requirements. The concept also explains why some salts appear "dry" yet lose mass when heated—they contain water that's chemically bound rather than free moisture.
Chemical indicators are substances that undergo reversible color changes in response to pH alterations, functioning as visual sensors for acidity or basicity. These compounds exist in different molecular forms depending on the hydrogen ion concentration in their environment, with each form displaying distinct colors. This property makes indicators invaluable tools for quickly determining whether solutions are acidic, basic, or neutral without requiring sophisticated instrumentation.
Litmus represents the oldest and most widely recognized indicator, extracted from lichen plants. The active component is a mixture of colored organic compounds. In solutions with pH below 7 (acidic), litmus appears red; in pH above 7 (basic), it turns blue. The transition occurs around pH 7, making litmus ideal for simple acid-base determination but unsuitable for precise pH measurement. Litmus is typically used by soaking paper in the extract, creating litmus paper—a staple of chemistry laboratories worldwide.
Phenolphthalein demonstrates a sharp color transition between pH 8.2 and 10.0, appearing colorless in acidic and neutral solutions but turning vivid pink in basic solutions. This narrow transition range makes phenolphthalein especially useful in titrations involving strong acids and weak bases, where the endpoint occurs in the basic region. Chemists prefer phenolphthalein when precise endpoint detection is required, as the color change is dramatic and easily observed even in dilute solutions.
Methyl orange transitions from red (pH below 3.1) to yellow (pH above 4.4), with orange appearing at intermediate pH values. This low pH transition range suits titrations of strong acids with weak bases, where the equivalence point occurs in the acidic region. The indicator's behavior reflects structural changes in the molecule as it gains or loses protons in response to solution pH.
Universal indicators represent sophisticated mixtures of multiple indicators that display different colors across the entire pH spectrum (0-14). These typically combine methyl red, bromothymol blue, thymol blue, and phenolphthalein among others, creating a rainbow of colors: red for strong acids, orange-yellow for weak acids, green for neutral, blue for weak bases, and violet for strong bases. Universal indicators enable approximate pH determination by matching the solution's color against a reference chart, providing pH values accurate to about ±1 unit.
Olfactory indicators represent an interesting alternative category that signals acids versus bases through smell changes rather than color. Onion extract, vanilla extract, and clove oil maintain their characteristic odors in acidic solutions but lose their smells in basic environments. These indicators work because bases chemically react with aromatic organic compounds, altering their molecular structure and destroying their odor-producing properties. While less common than visual indicators, olfactory indicators demonstrate the diverse ways chemical properties can signal environmental conditions.
The working principle underlying all pH indicators involves weak acid or base behavior. Indicator molecules themselves act as weak acids or bases that exist in equilibrium between protonated and deprotonated forms. Each form has distinct electronic structures and light absorption properties, resulting in different colors. When solution pH changes, the equilibrium shifts, altering the relative concentrations of the two forms and changing the observed color. This sophisticated molecular behavior, governed by principles of chemical equilibrium, enables the simple, practical applications that make indicators indispensable in chemistry education, research, and industrial quality control.
pH profoundly influences biological systems because most biochemical reactions and physiological processes function optimally only within narrow pH ranges. Enzymes—protein catalysts essential for life—exhibit extreme pH sensitivity, with their three-dimensional structures and catalytic activity depending critically on the precise hydrogen ion concentration in their environment. Even small pH deviations can denature enzymes, rendering them nonfunctional and disrupting metabolic pathways.
Human blood maintains a remarkably constant pH between 7.35 and 7.45, regulated through sophisticated buffering systems involving bicarbonate ions (HCO₃⁻), carbonic acid (H₂CO₃), and proteins. This slightly alkaline pH enables optimal oxygen binding to hemoglobin in the lungs and efficient oxygen release to tissues. Blood pH falling below 7.35 (acidosis) or rising above 7.45 (alkalosis) produces serious medical consequences including confusion, fatigue, irregular heartbeat, and in severe cases, coma or death. The body invests tremendous physiological resources maintaining blood pH homeostasis through respiratory regulation (exhaling CO₂ to reduce acidity) and kidney function (excreting excess acids or bases).
Digestive system pH varies dramatically by location, reflecting specialized functions. Stomach gastric juice has pH 1.0-3.0, creating an environment where pepsin enzymes break down proteins and harmful bacteria are killed. The small intestine maintains pH 7.5-8.5, suitable for pancreatic enzymes that digest carbohydrates and fats. When stomach acid production becomes excessive, pH drops further, causing heartburn and potentially ulcers. Antacids containing bases like magnesium hydroxide or calcium carbonate neutralize excess acid, raising pH back toward normal and providing symptom relief.
Oral health depends crucially on pH regulation. Tooth enamel, composed of calcium phosphate crystals, remains stable at neutral pH but dissolves when mouth pH drops below 5.5. Bacteria fermenting dietary sugars produce lactic acid and other organic acids that lower pH, initiating tooth decay. This explains why frequent sugar consumption and inadequate oral hygiene lead to cavities—the acid environment literally dissolves tooth structure. Using toothpaste containing basic compounds helps neutralize acid and remineralize enamel, protecting teeth.
Agricultural productivity relates directly to soil pH. Most crops thrive in slightly acidic to neutral soils (pH 6.0-7.5), where essential nutrients remain soluble and available for root absorption. Strongly acidic soils (pH below 5.5) cause aluminum and manganese toxicity while reducing availability of phosphorus, calcium, and magnesium. Strongly alkaline soils (pH above 8.5) create deficiencies of iron, manganese, and zinc. Farmers regularly test soil pH and apply amendments—lime to raise pH, sulfur to lower it—optimizing conditions for crop growth and maximizing yields.
Water quality for aquatic ecosystems requires appropriate pH maintenance. Most freshwater fish tolerate pH 6.5-8.5, with values outside this range causing stress, reduced reproduction, and mortality. Acid rain (pH below 5.6) from industrial sulfur and nitrogen oxide emissions acidifies lakes and streams, devastating aquatic life. Environmental regulations limiting these emissions and programs adding limestone to acidified waters aim to restore healthy pH levels.
Industrial processes across manufacturing sectors require precise pH control. Pharmaceutical production, chemical synthesis, food processing, textile dyeing, electroplating, and wastewater treatment all depend on maintaining specific pH conditions for optimal results, product quality, and regulatory compliance. Understanding pH principles enables informed decision-making in contexts from personal health to environmental protection to industrial operations.
Washing soda (sodium carbonate decahydrate, Na₂CO₃·10H₂O) and baking soda (sodium hydrogen carbonate or sodium bicarbonate, NaHCO₃) rank among the most versatile and widely used chemical compounds in households and industries. Despite their similar names and chemical relationship, they serve distinctly different purposes based on their chemical properties.
Washing soda is a moderately strong base with pH around 11 in aqueous solution. This alkalinity makes it highly effective for cleaning applications. In laundry, washing soda softens hard water by precipitating calcium and magnesium ions that interfere with detergent action, enhancing cleaning effectiveness. It cuts through grease and organic stains by saponifying fats (converting them to soap-like compounds) and raising pH to levels that break down proteins and other organic materials. Many commercial laundry boosters and heavy-duty cleaners incorporate washing soda as an active ingredient.
Industrial applications of washing soda include glass manufacturing, where it serves as a flux that lowers the melting point of silica sand, enabling more efficient production. The paper industry uses sodium carbonate in the kraft process for breaking down wood pulp. Water treatment facilities employ it to neutralize acidic water and precipitate undesirable heavy metals. Chemical manufacturers use washing soda as an intermediate in producing numerous sodium-based compounds.
Baking soda exhibits milder basicity (pH around 8.5) and unique thermal decomposition properties that drive its applications. When heated above 50°C, baking soda decomposes into sodium carbonate, water, and carbon dioxide gas: 2NaHCO₃ → Na₂CO₃ + H₂O + CO₂. This carbon dioxide release creates gas bubbles that cause dough to rise and baked goods to become light and fluffy.
Baking powder, a related product, combines baking soda with weak acids (cream of tartar or sodium aluminum sulfate) and starch. When moistened, the acid-base reaction releases CO₂ even without heating, providing "double-acting" leavening—once when wet, again when heated. This controlled gas release prevents premature reaction and ensures optimal texture in baked products.
Medical applications capitalize on baking soda's mild basicity and buffering capacity. As an antacid, it neutralizes excess stomach acid, providing relief from heartburn and indigestion. The reaction HCO₃⁻ + H⁺ → H₂O + CO₂ converts hydrochloric acid to water and carbon dioxide, raising gastric pH and reducing irritation. Baking soda mouthwash neutralizes bacterial acids that cause tooth decay and bad breath. Athletes sometimes consume small amounts before intense exercise, attempting to buffer lactic acid buildup in muscles, though this practice has mixed scientific support.
Fire extinguishers utilizing baking soda and acid (typically sulfuric acid) demonstrate practical chemistry. When activated, the acid-base reaction rapidly generates CO₂, which displaces oxygen and smothers small fires. This application leverages both the gas production from baking soda decomposition and carbon dioxide's fire-suppressing properties—being denser than air and non-supporting of combustion.
Personal care products incorporate baking soda as a gentle abrasive in toothpastes and skin cleansers, while its odor-neutralizing properties make it popular in deodorants and refrigerator fresheners. The compound's safety profile, low cost, and versatility explain its ubiquity in consumer products and its status as a household staple for generations.
Plaster of Paris (calcium sulfate hemihydrate, CaSO₄·½H₂O) represents a fascinating material whose useful properties stem directly from its relationship with gypsum (calcium sulfate dihydrate, CaSO₄·2H₂O) and the reversible nature of its hydration reaction. Understanding this chemistry explains both its preparation and its practical applications in construction, medicine, and art.
The manufacturing process begins with natural gypsum deposits—sedimentary rocks containing calcium sulfate dihydrate formed from ancient marine evaporation. When heated to approximately 373 K (100°C), gypsum loses 75% of its water of crystallization through a carefully controlled dehydration process: 2(CaSO₄·2H₂O) → 2(CaSO₄·½H₂O) + 3H₂O. Temperature control is critical—excessive heating (above 473 K) removes all water, producing anhydrous calcium sulfate or "dead burnt plaster," which rehydrates extremely slowly and lacks useful setting properties.
The resulting Plaster of Paris appears as a fine white powder with distinctive physical properties. When mixed with water (typically at a water-to-plaster ratio of 0.5-0.8), a remarkable transformation occurs: the powder and water combine to form a smooth, workable paste that remains moldable for 10-20 minutes before rapidly hardening into a solid mass. This setting process represents the reverse of the dehydration reaction: CaSO₄·½H₂O + 1½H₂O → CaSO₄·2H₂O, converting Plaster of Paris back into gypsum.
The chemistry underlying this hardening involves several fascinating phenomena. Initially, when water contacts the powder, calcium sulfate hemihydrate dissolves, creating a supersaturated solution. As the dissolved material reaches saturation, gypsum crystals begin nucleating and growing. These needle-like crystals interlock in three-dimensional networks, forming a rigid structure that entraps remaining water. The process is exothermic—chemical energy released during hydration manifests as heat, making the setting mass noticeably warm. This heat acceleration can shorten working time in warm environments.
Crucially, Plaster of Paris expands slightly (approximately 0.3%) during setting, unlike most materials that contract. This expansion occurs because the gypsum crystal structure occupies more volume than the hydrated calcium sulfate ions in solution. This property makes Plaster of Paris ideal for mold-making and casting—it presses into every detail of the original surface, producing faithful reproductions without pulling away from edges as contracting materials would.
Medical applications exploit these setting properties for immobilizing broken bones. Plaster-impregnated gauze bandages, when moistened and wrapped around injured limbs, conform perfectly to body contours while wet. Within 10-15 minutes, the material hardens into a rigid, supportive cast that maintains bone alignment during healing. The slight warmth during setting is generally tolerable, though excessive heat occasionally necessitates cooling. Modern fiberglass casts have partially replaced plaster due to lighter weight and water resistance, but plaster casts remain valuable for their superior moldability for complex fractures and lower cost.
Construction and art applications include creating decorative ceiling moldings, producing sculpture replicas, manufacturing architectural models, and preparing smooth wall surfaces. The material's low cost, ease of use, and ability to capture fine detail make it irreplaceable despite the availability of modern synthetic materials. However, set plaster exhibits poor water resistance—extended moisture exposure softens it, limiting outdoor applications unless properly sealed.
Temperature significantly affects setting time: cold conditions slow the reaction, while warmth accelerates it. Additives can modify working time—salt or alum speeds setting, while borax or citric acid retards it, giving artisans greater control. Understanding these chemical principles allows users to optimize Plaster of Paris for specific applications, balancing workability against the need for rapid hardening.