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📌 Illustrated Diagram: Colligative Properties
Solutions – Complete CBSE Class 12 Chemistry Notes
Unit 1 | Solutions | CBSE 2026–27
A solution is a homogeneous mixture. In a binary solution, the solvent is the component present in larger amount and the solute is the component dissolved in it.
1. Concentration of Solutions
| Term | Formula | Important point |
|---|---|---|
| Molarity (M) | moles of solute / volume of solution in L | Temperature dependent |
| Molality (m) | moles of solute / mass of solvent in kg | Temperature independent |
| Mole fraction | xᵢ = nᵢ / Σn | Dimensionless |
| Mass % | mass of component / mass of solution × 100 | Useful for composition |
Worked Example 1
5.85 g NaCl (molar mass 58.5 g mol⁻¹) is present in 500 mL solution. Moles = 5.85/58.5 = 0.10 mol. Therefore M = 0.10/0.500 = 0.20 M.
2. Solubility and Henry’s Law
The solubility of a gas in a liquid generally increases with pressure. Henry’s law is written as p = KHx. This explains why carbonated drinks are bottled under pressure and why divers can experience problems when dissolved gases come out of solution rapidly.
3. Vapour Pressure and Raoult’s Law
For an ideal solution, the partial vapour pressure of a volatile component is proportional to its mole fraction: pᵢ = xᵢpᵢ°. For a solution containing a non-volatile solute, the vapour pressure of the solvent decreases.
4. Ideal vs Non-Ideal Solutions
| Ideal | Positive deviation | Negative deviation |
|---|---|---|
| Obeys Raoult’s law | A–B attraction weaker than expected | A–B attraction stronger than expected |
| ΔHmix ≈ 0 | Vapour pressure higher | Vapour pressure lower |
5. Colligative Properties
These depend primarily on the number of solute particles: relative lowering of vapour pressure, elevation of boiling point, depression of freezing point and osmotic pressure.
ΔTb = iKbm ΔTf = iKfm π = iCRT
Worked Example 2
For a non-electrolyte solution with m = 0.50 mol kg⁻¹ and Kf = 1.86 K kg mol⁻¹, ΔTf = 1.86 × 0.50 = 0.93 K.
6. van’t Hoff Factor
Association decreases the number of particles, while dissociation increases it. The factor i accounts for this abnormal particle count. For example, ideal NaCl dissociation gives approximately two ions per formula unit, so i may approach 2 in the appropriate dilute limit.
🧠 Visual Concept Map
📝 Competency Practice
- A student calculates molarity before and after heating a solution. Explain why molarity can change even when the amount of solute remains constant.
- Why are soft drinks stored under pressure?
- A solute associates in solution. Predict the direction of change in observed molar mass.
- Explain why osmotic pressure is useful for determining molar mass of large molecules.
🎯 Board-Style Numericals
- Calculate molality when 18 g glucose (180 g mol⁻¹) is dissolved in 500 g water.
- Calculate ΔTf for a specified molality and Kf.
- Use osmotic pressure data to calculate molar mass.
- Determine the van’t Hoff factor from observed freezing-point depression.
MCQs – Chapter Specific
- Which concentration is based on mass of solvent? Molality.
- Which law relates gas pressure and mole fraction in solution? Henry’s law.
- A non-volatile solute generally lowers the solvent’s vapour pressure. True.
- If a solute dissociates into more particles, the van’t Hoff factor tends to be greater than 1. True.
Deep-Dive: Core Concepts & Numericals
Concentration Terms
Molarity is moles of solute per litre of solution, while molality is moles of solute per kilogram of solvent. Mole fraction is the ratio of moles of a component to total moles. Always identify whether the question gives solution volume or solvent mass before choosing the formula.
Worked Numerical
For 0.5 mol solute dissolved to make 2 L solution, M=0.5/2=0.25 mol L⁻¹.
Colligative Properties
Relative lowering of vapour pressure, elevation of boiling point, depression of freezing point and osmotic pressure depend on the number of solute particles. For dilute solutions, ΔT_b=K_bm and ΔT_f=K_fm.
Visual Map
Boiling point ↑ Freezing point ↓ Vapour pressure ↓
Common Mistakes
- Confusing molarity with molality.
- Using mass of solution instead of mass of solvent for molality.
- Forgetting van’t Hoff factor for association/dissociation.
Practice
- Calculate molarity and molality from given masses.
- Apply Raoult’s law to a binary solution.
- Calculate elevation/depression of temperature.
- Determine molar mass using osmotic pressure.
Concept Builder: Solutions
Concentration Terms
Use molarity, molality, mole fraction and mass percentage carefully. Molarity depends on volume of solution, while molality depends on mass of solvent and is therefore less affected by temperature.
Raoult’s Law — Visual
Adding non-volatile solute → vapour pressure decreases
Colligative Properties
For dilute solutions, elevation in boiling point and depression in freezing point depend on the number of solute particles. For association or dissociation, the van’t Hoff factor i must be considered.
Worked Numerical
For a solution with molality 0.50 m and Kf=1.86 K kg mol−1, assuming i=1, ΔTf=Kfm=1.86×0.50=0.93 K.
Exam Traps
- Do not confuse molarity with molality.
- Use the van’t Hoff factor when solute particles associate or dissociate.
- Check whether the question gives mass of solvent or solution.
CBSE Application Practice
- Calculate molality from masses of solute and solvent.
- Determine molar mass from elevation/depression data.
- Explain abnormal molar mass using i.
- Interpret a vapour-pressure graph.
