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Saturday, 24 May 2025

Module 3: Acidic and Basic Nature – The pH Concept

 

๐ŸŒŸ Module 3: Acidic and Basic Nature – The pH Concept


๐ŸŽฏ Objective:

To understand the pH scale, its scientific basis, and how acidic or basic nature of substances impacts daily life—ranging from the human body to agriculture and environment.


๐Ÿ”ฌ 1. What is pH?

๐Ÿ”น The term pH stands for "potential of Hydrogen" or "power of Hydrogen".

๐Ÿ”น It is a measure of hydrogen ion concentration [H+][H⁺] in a solution.

๐Ÿ”น pH is a logarithmic scale:

pH=log10[H+]\text{pH} = -\log_{10}[H^+]
  • If [H+][H^+] is high → pH is lowAcidic.

  • If [OH][OH^-] is high → pH is highBasic (Alkaline).


๐Ÿ“ˆ 2. The pH Scale (0–14)

pH ValueNature of SubstanceExampleUniversal Indicator Color
0 – 3Strongly AcidicHydrochloric acid (HCl), gastric juiceRed / Dark Orange
4 – 6Weakly AcidicTomato juice, vinegarOrange to Yellow
7NeutralPure waterGreen
8 – 10Weakly BasicBaking soda solutionBlue
11 – 14Strongly BasicNaOH, KOH solutionsPurple / Violet

๐Ÿง  Concept Insight:

  • pH < 7 → Acidic

  • pH = 7 → Neutral

  • pH > 7 → Basic

The farther from 7, the stronger the acid/base.


๐ŸŒฟ 3. Importance of pH in Everyday Life


๐Ÿ‘ค a. pH in the Human Body

  • The human body maintains a blood pH around 7.35–7.45.

  • Enzymes, hormones, and cell functions require stable pH.

  • Drastic changes in pH can be fatal (acidosis or alkalosis).

๐Ÿ” Example:

  • Stomach acid has a pH of 1.5–3.5 for digestion (HCl).

  • Antacids like milk of magnesia (Mg(OH)₂) are basic to neutralize excess acid.


๐ŸŒฑ b. pH of Soil for Plants

  • Soil pH affects nutrient absorption.

  • Most crops grow well in pH 6 to 7.5.

  • Too acidic soil → Add quicklime (CaO).

  • Too basic soil → Add organic matter or sulfur.

๐Ÿ” Example:

  • Tea grows well in acidic soils (pH < 6).

  • Farmers often test soil pH before fertilizing.


๐Ÿฆท c. Tooth Decay and pH

  • Bacteria in the mouth produce acids after eating sugary foods.

  • If pH of mouth falls below 5.5, tooth enamel starts dissolving.

  • Toothpastes are basic to neutralize this acid and prevent cavities.


d. Acid Rain

  • Pollutants like SO₂ and NO₂ dissolve in rainwater to form H₂SO₄ and HNO₃.

  • Rainwater becomes acidic (pH < 5.6) → Damages buildings, crops, aquatic life.

๐Ÿ” Equation:

SO2+H2OH2SO3\text{SO}_2 + \text{H}_2O \rightarrow \text{H}_2\text{SO}_3 H2SO3+[O]H2SO4\text{H}_2\text{SO}_3 + [O] \rightarrow \text{H}_2\text{SO}_4


๐ŸŒˆ 4. Universal Indicator and pH Colors

  • A universal indicator is a mixture of several indicators that shows a range of colors for different pH levels.

๐Ÿ“Š Color Guide:

pHColorNature
1RedStrong acid
4OrangeWeak acid
7GreenNeutral
9BlueWeak base
13PurpleStrong base

๐Ÿงช 5. Demonstration Activity – pH Testing

๐ŸŽฒ Materials:

  • Universal indicator paper

  • Solutions: Vinegar, soap water, lemon juice, milk, baking soda, cola, shampoo, detergent

  • Small containers

๐Ÿ”ฌ Procedure:

  1. Dip the indicator strip into each liquid.

  2. Compare the color with the standard pH color chart.

  3. Record observations.

๐Ÿ“‹ Sample Observations:

SubstancepH RangeIndicator ColorNature
Vinegar3Orange-RedAcidic
Lemon juice2–3RedAcidic
Soap water9–10BlueBasic
Milk6.5–6.8Pale Yellow-GreenSlightly acidic
Baking soda8–9Blue-GreenWeak base
Cola2–3RedStrong acid
Shampoo5–6YellowMild acid

๐Ÿ’ก Misconception Alert

  • A lower pH does NOT mean a “better acid”—it means a stronger acid.

  • Acidic ≠ sour taste only. Some acids are dangerous to taste or touch.

  • Not all alkaline solutions feel slippery. Some can be corrosive, like NaOH.


๐Ÿง  Quick Revision Capsule

  • pH measures acidity/basicity using hydrogen ion concentration.

  • Universal indicator helps determine pH through color change.

  • Neutralization reactions help in controlling pH in soil, mouth, and body.

  • pH control is essential in agriculture, healthcare, and environment.

Friday, 23 May 2025

Module 2: Chemical Properties of Acids and Bases

 

๐ŸŒŸ Module 2: Chemical Properties of Acids and Bases

Chapter: Acids, Bases and Salts – Class 10 Science (CBSE)


๐ŸŽฏ Objective:

To understand the chemical behaviour of acids and bases with various classes of compounds including metals, metal oxides, metal carbonates, and non-metal oxides, through balanced chemical equations and real-life examples.


๐Ÿ”ฌ 1. Reaction of Acids with Metals

๐Ÿ”น General Reaction:

Acid+MetalSalt+Hydrogen gas (H₂↑)\text{Acid} + \text{Metal} \rightarrow \text{Salt} + \text{Hydrogen gas (H₂↑)}

Example:

Zn+2HClZnCl2+H2\text{Zn} + 2\text{HCl} \rightarrow \text{ZnCl}_2 + \text{H}_2↑
  • Hydrogen gas is evolved – it can be tested by bringing a burning splint near the mouth of the test tube. A ‘pop’ sound confirms hydrogen.

  • Salt formed depends on the acid and metal used.

๐Ÿง  Concept Insight:

Metals displace hydrogen from acids because they are more electropositive. This is a single displacement reaction.


๐Ÿงช 2. Reaction of Acids with Metal Carbonates and Bicarbonates

๐Ÿ”น General Reactions:

Acid+Metal carbonateSalt+Carbon dioxide (CO₂)+Water\text{Acid} + \text{Metal carbonate} \rightarrow \text{Salt} + \text{Carbon dioxide (CO₂)} + \text{Water}
Acid+Metal bicarbonateSalt+CO2+H2O\text{Acid} + \text{Metal bicarbonate} \rightarrow \text{Salt} + \text{CO}_2 + \text{H}_2O

Example 1:

Na2CO3+2HCl2NaCl+CO2+H2O\text{Na}_2\text{CO}_3 + 2\text{HCl} \rightarrow 2\text{NaCl} + \text{CO}_2↑ + \text{H}_2O

Example 2:

NaHCO3+HClNaCl+CO2+H2O\text{NaHCO}_3 + \text{HCl} \rightarrow \text{NaCl} + \text{CO}_2↑ + \text{H}_2O

๐Ÿ” CO₂ Detection Test:

Pass the evolved gas through lime water (Ca(OH)₂). If it turns milky, CO₂ is present:

Ca(OH)2+CO2CaCO3+H2O\text{Ca(OH)}_2 + \text{CO}_2 \rightarrow \text{CaCO}_3↓ + \text{H}_2O


๐Ÿ”ฅ 3. Reaction of Acids with Metal Oxides (Basic Oxides)

Metal oxides are basic in nature and neutralize acids.

๐Ÿ”น General Reaction:

Acid+Metal oxideSalt+Water\text{Acid} + \text{Metal oxide} \rightarrow \text{Salt} + \text{Water}

Example:

2HCl+CuOCuCl2+H2O2\text{HCl} + \text{CuO} \rightarrow \text{CuCl}_2 + \text{H}_2O

๐Ÿง  Concept Insight:
This is a neutralisation reaction where metal oxides act like bases.


๐ŸŒซ️ 4. Reaction of Bases with Non-metal Oxides (Acidic Oxides)

Non-metal oxides like CO₂ are acidic in nature and react with bases.

๐Ÿ”น General Reaction:

Base+Non-metal oxideSalt+Water\text{Base} + \text{Non-metal oxide} \rightarrow \text{Salt} + \text{Water}

Example:

Ca(OH)2+CO2CaCO3+H2O\text{Ca(OH)}_2 + \text{CO}_2 \rightarrow \text{CaCO}_3 + \text{H}_2O
  • This reaction also forms insoluble calcium carbonate, making lime water turn milky.

  • Indicates that CO₂ behaves as an acidic oxide.


๐Ÿงช Activity: Baking Soda and Vinegar Reaction

๐ŸŽฒ Materials:

  • Baking soda (sodium bicarbonate – NaHCO₃)

  • Vinegar (contains acetic acid – CH₃COOH)

  • Transparent glass

  • Spoon

๐Ÿงช Procedure:

  1. Take 1 spoon of baking soda in a glass.

  2. Add 2–3 spoons of vinegar.

  3. Observe the fizzing and bubble formation.

๐Ÿ”ฌ Reaction:

NaHCO3+CH3COOHCH3COONa+CO2+H2O\text{NaHCO}_3 + \text{CH}_3\text{COOH} \rightarrow \text{CH}_3\text{COONa} + \text{CO}_2↑ + \text{H}_2O

๐Ÿ’ก Observation:

  • CO₂ gas causes fizzing.

  • It is the same principle used in baking, where CO₂ causes dough to rise.


๐Ÿ“Œ Summary of Key Reactions

Reaction TypeExample Equation
Acid + MetalZn + HCl → ZnCl₂ + H₂
Acid + Carbonate/BicarbonateNa₂CO₃ + HCl → NaCl + CO₂ + H₂O
Acid + Metal OxideCuO + HCl → CuCl₂ + H₂O
Base + Non-metal OxideCa(OH)₂ + CO₂ → CaCO₃ + H₂O


๐Ÿง  Think Like a Scientist

๐Ÿ”น Q: Why is CO₂ treated as an acidic oxide?

๐Ÿ”น A: Because it reacts with bases to form salt and water—just like an acid.

๐Ÿ”น Q: Why is fizzing seen when vinegar is added to baking soda?

๐Ÿ”น A: Because CO₂ gas is released due to acid-base neutralisation.


๐Ÿง  Misconceptions Cleared

  • Not all metal oxides are acidic; metal oxides are generally basic.

  • Not all acids react with all metals—unreactive metals like copper do not displace hydrogen from dilute acids like HCl.

  • Baking soda is a weak base, not a neutral compound.

Module 1: Introduction to Acids and Bases

 

๐Ÿ”ฌ Module 1: Introduction to Acids and Bases

(Class 10 CBSE Science – Chapter: Acids, Bases, and Salts)


๐ŸŒŸ 1. What are Acids and Bases?

Acids and Bases are two important categories of chemical substances that show distinctly different chemical and physical properties.

๐Ÿ“˜ Definition:

  • Acids: Substances that release hydrogen ions (H⁺) in an aqueous solution.
    Example: Hydrochloric acid (HCl) dissociates in water as:
    HCl → H⁺ + Cl⁻

  • Bases: Substances that release hydroxide ions (OH⁻) in an aqueous solution.
    Example: Sodium hydroxide (NaOH) dissociates as:
    NaOH → Na⁺ + OH⁻

๐Ÿ“Œ Note: The presence of H⁺ or OH⁻ ions in water is responsible for the acidic or basic nature of the substance.


๐Ÿ” 2. Physical Properties

PropertyAcidsBases
TasteSour (Don't taste in lab!)Bitter (Don't taste in lab!)
TouchCorrosiveSoapy or slippery
Effect on litmusTurns blue to redTurns red to blue
Electrical conductivityGood conductor (due to H⁺ ions)Good conductor (due to OH⁻ ions)


๐Ÿงช 3. Common Examples from Daily Life

AcidsBases
Lemon juice (citric acid)Soap (sodium hydroxide)
Vinegar (acetic acid)Baking soda (sodium bicarbonate)
Curd (lactic acid)Toothpaste (mild base)
Tamarind (tartaric acid)Limewater (calcium hydroxide)


๐Ÿงซ 4. Indicators: Detecting Acids and Bases

Indicators are substances that change color in acidic or basic media. They help to identify whether a given solution is acidic or basic.

๐Ÿ”น Types of Indicators:

IndicatorAcidic SolutionBasic Solution
LitmusBlue → RedRed → Blue
PhenolphthaleinColorlessPink
Methyl OrangeRedYellow


Natural Indicators: Litmus (from lichens), turmeric, red cabbage

Synthetic Indicators: Phenolphthalein, Methyl orange


๐Ÿ” 5. Acid-Base Reactions with Indicators (Visual Table)

SubstanceEffect on LitmusEffect on PhenolphthaleinEffect on Methyl Orange
Hydrochloric acidBlue → RedColorlessRed
Sodium hydroxideRed → BluePinkYellow
Lemon juiceBlue → RedColorlessRed
Soap solutionRed → BluePinkYellow


๐ŸŽฏ 6. Key Scientific Concepts
  • Arrhenius Theory:

    • Acids: Produce H⁺ in water.

    • Bases: Produce OH⁻ in water.

  • Neutralisation Reaction:

    • Acid + Base → Salt + Water
      HCl + NaOH → NaCl + H₂O


๐Ÿ“š 7. Misconceptions Cleared

  • Acids are not always dangerous. Many are edible and found in food (like citric acid).

  • Not all substances that feel slippery are bases (e.g., oil is slippery but not basic).

  • Indicators are tools, not proof of concentration or strength—just the presence of H⁺ or OH⁻ ions.


๐Ÿง  8. Thinking Corner

Why do ant bites cause a burning sensation, and how does applying baking soda help?

Answer: Ant sting injects formic acid (acidic). Baking soda (a base) neutralizes the acid, relieving the pain.


๐Ÿงช Hands-on Activity (Home/Lab)

Name: Testing Acids and Bases Using Indicators
Materials: Red/blue litmus paper, lemon juice, baking soda solution, soap, vinegar, shampoo
Procedure: Dip litmus in each solution and record color changes
Conclusion: Identify acidic and basic substances


๐Ÿ“Œ Summary Points

  • Acids and bases are classified based on the release of H⁺ and OH⁻ ions respectively.

  • Physical characteristics help in identification but are not to be tested manually.

  • Indicators help detect the acidic or basic nature of substances.

  • Some substances can behave as acids or bases depending on the environment (amphoteric substances – to be studied later).

Expressing Concentration of Solutions

 

๐Ÿ“˜ Expressing Concentration of Solutions

The composition of a solution refers to the relative amount of solute and solvent present in it. This composition can be expressed in two main ways:

  • Qualitatively

  • Quantitatively


๐Ÿ”น Qualitative Description

This is a non-numerical way of expressing the concentration. For example:

  • A dilute solution has a relatively small amount of solute.

  • A concentrated solution has a relatively large amount of solute.

However, qualitative terms are vague and can lead to confusion, especially in scientific or industrial applications. Hence, quantitative expressions of concentration are preferred.


๐Ÿ”น Quantitative Description

Several methods are used to express the concentration of a solution quantitatively:


(i) Mass Percentage (% w/w)

Definition:

Mass % of a component=(Mass of the component in the solutionTotal mass of the solution)×100\text{Mass \% of a component} = \left( \frac{\text{Mass of the component in the solution}}{\text{Total mass of the solution}} \right) \times 100

Example:
A solution of 10% glucose by mass means:

  • 10 g of glucose (solute)

  • 90 g of water (solvent)
    Total mass = 100 g

Application:
Mass percentage is commonly used in industrial applications.
E.g., Commercial bleaching solution contains 3.62% NaOCl (sodium hypochlorite) by mass.


(ii) Volume Percentage (% v/v)

Definition:

Volume % of a component=(Volume of the componentTotal volume of the solution)×100\text{Volume \% of a component} = \left( \frac{\text{Volume of the component}}{\text{Total volume of the solution}} \right) \times 100

Example:
A 10% ethanol solution by volume means:

  • 10 mL ethanol

  • Water added to make the total volume = 100 mL

Application:
Used for liquid–liquid solutions like:

  • Antifreeze: A 35% (v/v) ethylene glycol solution lowers the freezing point of water to 255.4 K (-17.6°C).


(iii) Mass by Volume Percentage (% w/v)

Definition:

Mass by Volume %=(Mass of solute in gramsVolume of solution in mL)×100\text{Mass by Volume \%} = \left( \frac{\text{Mass of solute in grams}}{\text{Volume of solution in mL}} \right) \times 100

Application:
Commonly used in medicine and pharmacy.
E.g., A 5% w/v solution means 5 g of solute in 100 mL of solution.


(iv) Parts per Million (ppm)

Definition:

ppm=(Number of parts of the componentTotal number of parts of all components)×106\text{ppm} = \left( \frac{\text{Number of parts of the component}}{\text{Total number of parts of all components}} \right) \times 10^6

Application:
Used for very low concentrations (trace quantities), especially in:

  • Environmental chemistry

  • Pollution analysis
    E.g., Sea water (1030 g) contains 6 × 10⁻³ g of dissolved O₂

ppm=6×1031030×1065.8 ppm\text{ppm} = \frac{6 \times 10^{-3}}{1030} \times 10^6 \approx 5.8\ ppm

Variants: ppm can be:

  • mass to mass

  • volume to volume

  • mass to volume


(v) Mole Fraction (ฯ‡)

Definition:

ฯ‡i=nini\chi_i = \frac{n_i}{\sum n_i}

Where:

  • nin_i = number of moles of component i

  • ni\sum n_i = total moles of all components

In a binary mixture of components A and B:

ฯ‡A=nAnA+nB,ฯ‡B=nBnA+nB\chi_A = \frac{n_A}{n_A + n_B}, \quad \chi_B = \frac{n_B}{n_A + n_B} ฯ‡A+ฯ‡B=1\chi_A + \chi_B = 1

Application:
Useful in calculating vapor pressure, colligative properties, and gas mixture compositions.


(vi) Molarity (M)

Definition:

Molarity (M)=Moles of soluteVolume of solution in litre\text{Molarity (M)} = \frac{\text{Moles of solute}}{\text{Volume of solution in litre}}

Example:
0.25 M NaOH means 0.25 mol of NaOH is dissolved in 1 litre of solution.

Note:
Temperature-dependent because volume changes with temperature.


(vii) Molality (m)

Definition:

Molality (m)=Moles of soluteMass of solvent in kg\text{Molality (m)} = \frac{\text{Moles of solute}}{\text{Mass of solvent in kg}}

Example:
A 1.00 m solution of KCl means 1 mol (74.5 g) of KCl is dissolved in 1 kg of water.

Note:
Independent of temperature because it involves mass, not volume.


๐Ÿ“ Summary Table

ExpressionSymbolFormulaDepends on Temperature?Typical Use
Mass % (w/w)Mass of soluteTotal mass of solution×100\frac{\text{Mass of solute}}{\text{Total mass of solution}} \times 100
❌ NoIndustrial mixtures
Volume % (v/v)Volume of soluteTotal volume of solution×100\frac{\text{Volume of solute}}{\text{Total volume of solution}} \times 100
✅ YesLiquid-liquid solutions
Mass/Volume % (w/v)Mass of soluteVolume of solution in mL×100\frac{\text{Mass of solute}}{\text{Volume of solution in mL}} \times 100
✅ YesMedical & pharmaceutical use
Parts per million (ppm)
Part of soluteTotal parts of solution×106\frac{\text{Part of solute}}{\text{Total parts of solution}} \times 10^6
❌ NoEnvironmental concentrations
Mole fractionฯ‡\chi
Moles of componentTotal moles of solution\frac{\text{Moles of component}}{\text{Total moles of solution}}❌ NoGas mixtures, vapor pressure
MolarityMMoles of soluteVolume of solution in litres\frac{\text{Moles of solute}}{\text{Volume of solution in litres}}✅ YesTitrations, lab solutions
MolalitymMoles of soluteMass of solvent in kg\frac{\text{Moles of solute}}{\text{Mass of solvent in kg}}❌ NoColligative property calculations

๐Ÿ” Conclusion

  • Each unit has its specific application depending on the accuracy, temperature dependence, and nature of the solution.

  • Mass %, ppm, mole fraction, and molality are independent of temperature, making them more reliable in changing environments.

  • Molarity, while commonly used, must be handled carefully with temperature-sensitive systems.

Azeotropes – Explained for Class 12 (CBSE Chemistry)

 

๐Ÿ“˜ Azeotropes – Explained for Class 12 (CBSE Chemistry)


๐Ÿ”น What is an Azeotrope?

An azeotrope is a mixture of two (or more) liquids that boils at a constant temperature and behaves like a pure substance during boiling.

๐Ÿงช Definition:

An azeotrope is a binary mixture that boils at a constant temperature and produces vapour with the same composition as the liquid.

This means you cannot separate the two components by simple distillation — they behave as one compound at that specific composition and boiling point.


๐Ÿ” Why does this happen?

Normally, during boiling, the composition of vapour differs from that of liquid (more volatile component escapes faster). But in an azeotropic mixture, this difference disappears at a certain fixed composition — the vapour formed has the same ratio of both components as in the liquid. Hence, no further separation by boiling is possible.


๐ŸŒก️ Types of Azeotropes

Azeotropes are mainly of two types based on their boiling points in comparison to their pure components:


(i) Minimum Boiling Azeotropes

  • These mixtures boil at a lower temperature than either of the pure components.

  • They show positive deviation from Raoult’s Law (the components escape more easily due to weaker interactions).

  • The total vapour pressure is higher, so they boil at a lower temperature.

๐Ÿงช Example:

  • Ethanol (95%) + Water (5%)

  • Boiling Point ≈ 351 K (78°C)

  • This mixture forms an azeotrope that cannot be separated further by simple distillation.

๐Ÿง  Reason:

Ethanol and water form weaker hydrogen bonds in the mixture than in the pure liquids, so they escape more easily → higher vapour pressure → lower boiling point.


(ii) Maximum Boiling Azeotropes

  • These mixtures boil at a higher temperature than either of the pure components.

  • They show negative deviation from Raoult’s Law (the components strongly attract each other).

  • The total vapour pressure is lower, so they boil at a higher temperature.

๐Ÿงช Example:

  • Nitric acid (68%) + Water (32%)

  • Boiling Point ≈ 393.5 K (120.5°C)

๐Ÿง  Reason:

Strong hydrogen bonding between nitric acid and water lowers the escaping tendency → lower vapour pressure → higher boiling point.


๐Ÿ“Š Comparison Table:


Type

Boiling Point

Deviation from Raoult's Law

Vapour Pressure

Example

Minimum Boiling Azeotrope

Lower than components

Positive Deviation

High

Ethanol + Water (95%)

Maximum Boiling Azeotrope

Higher than components

Negative Deviation

Low

Nitric Acid + Water (68%)


๐ŸŽ“ Real-life Importance

  • Azeotropes limit the extent of separation by distillation.

  • Special methods like azeotropic distillation or adding third components (entrainers) are used in industries to break azeotropes.

  • Ethanol production: 95% ethanol + 5% water azeotrope is common in alcohol distillation.


๐Ÿ’ก Analogy to Understand

Think of azeotropes as inseparable couples:

  • In a normal couple (mixture), one partner might leave early (more volatile component distills first).

  • In an azeotrope, both are so balanced in their interactions that they leave together, hand in hand, at the same time (same composition in vapour and liquid).

Raoult’s Law and Henry’s Law – A Comparative Study

 

1. Raoult’s Law

Raoult’s law is applicable to solutions containing volatile components. It states:

"The partial vapour pressure of each volatile component in a solution is directly proportional to its mole fraction."

Mathematical Expression:

For a component 1 in a binary solution:

p1=x1p10p_1 = x_1 \cdot p_1^0

Where:

  • p1p_1 = Partial vapour pressure of component 1 in the solution

  • x1x_1 = Mole fraction of component 1 in the solution

  • p10p_1^0 = Vapour pressure of pure component 1


2. Henry’s Law

Henry’s Law is applicable to gases dissolved in liquids. It states:

"The partial pressure of the gas (p) in the vapour phase is directly proportional to its mole fraction (x) in the solution."

Mathematical Expression:

p=KHxp = K_H \cdot x

Where:

  • pp = Partial pressure of the gas

  • xx = Mole fraction of the gas in solution

  • KHK_H = Henry’s Law constant


3. Raoult’s Law as a Special Case of Henry’s Law

  • Both laws show a direct proportionality between partial pressure and mole fraction.

  • In Raoult’s law, the constant of proportionality is p10p_1^0, while in Henry’s law it is KHK_H.

  • Hence, Raoult’s law can be considered a special case of Henry’s law when KH=p10K_H = p_1^0.


4. Vapour Pressure of Solutions

(a) Pure Solvent

  • Molecules escape from the surface and exert vapour pressure at equilibrium.

(b) Solution with a Non-Volatile Solute

  • When a non-volatile solute is added, the vapour pressure decreases.

  • Fewer solvent molecules are available at the surface to escape into vapour phase.

Key Point:

  • The reduction in vapour pressure depends only on the quantity of solute and not on its nature.


5. Ideal and Non-Ideal Solutions

(A) Ideal Solutions

Definition: Solutions that obey Raoult’s law over the entire concentration range.

Characteristics:

  • ฮ”mixH=0\Delta_{\text{mix}} H = 0 (No heat is evolved or absorbed)

  • ฮ”mixV=0\Delta_{\text{mix}} V = 0 (No change in volume on mixing)

  • Intermolecular forces: A–A ≈ B–B ≈ A–B

Examples:

  • Benzene and Toluene

  • n-Hexane and n-Heptane


(B) Non-Ideal Solutions

Definition: Solutions that deviate from Raoult’s law.

They show either:

(i) Positive Deviation

  • psolution>pexpectedp_{\text{solution}} > p_{\text{expected}}

  • A–B interactions < A–A and B–B interactions

  • More molecules escape → Higher vapour pressure

Examples:

  • Ethanol + Acetone

  • Acetone + Carbon Disulphide

(ii) Negative Deviation

  • psolution<pexpectedp_{\text{solution}} < p_{\text{expected}}

  • A–B interactions > A–A and B–B interactions

  • Fewer molecules escape → Lower vapour pressure

Examples:

  • Chloroform + Acetone (Hydrogen bonding between components)

  • Phenol + Aniline


6. Azeotropes

Definition: Binary mixtures that boil at a constant temperature and whose liquid and vapour phases have the same composition.

Types of Azeotropes:

(i) Minimum Boiling Azeotropes

  • Show positive deviation

  • Boil at a lower temperature than both components

Example:

  • Ethanol (95%) + Water → Boiling point: ~351 K

(ii) Maximum Boiling Azeotropes

  • Show negative deviation

  • Boil at a higher temperature than both components

Example:

  • Nitric acid (68%) + Water → Boiling point: 393.5 K


7. Graphical Representations

(i) Raoult’s Law for Ideal Solutions

  • Linear plot of vapour pressure vs. mole fraction

(ii) Non-Ideal Solutions

  • Positive Deviation: Upward curve (convex)

  • Negative Deviation: Downward curve (concave)

Summary Table

TypeDeviationA-B InteractionVapour PressureExample
Ideal SolutionNoneA–B ≈ A–A ≈ B–BMatches Raoult’s lawBenzene + Toluene
Non-Ideal (+ve)PositiveA–B < A–A or B–BGreater than expectedEthanol + Acetone
Non-Ideal (–ve)NegativeA–B > A–A or B–BLess than expectedChloroform + Acetone
Min. Boiling AzeotropePositiveWeak A–BBoils below both liquidsEthanol (95%) + Water
Max. Boiling AzeotropeNegativeStrong A–BBoils above both liquidsNitric Acid (68%) + Water


Conclusion

Raoult’s law and Henry’s law both describe the relationship between vapour pressure and mole fraction, although applicable in different contexts (liquids vs. gases). Understanding deviations from Raoult’s law helps us classify solutions as ideal or non-ideal and explains the formation of azeotropes, which are critical in processes like distillation.