Freezing point depression
ΔT_f = K_f × m, where K_f is cryoscopic constant (water: 1.86 K·kg/mol). Used to determine molar mass of solute.
-- NCERT Class 12 Chemistry, Ch. 1, p. 20Here is the trap that costs marks on this topic: you see NaCl or CaCl₂ in the stem, calculate ΔT_f using the plain formula, and forget to multiply by the Van't Hoff factor i. That single omission produces a distractor that NTA places among the options every time this topic appears.
The core idea. A non-volatile solute dissolved in a solvent lowers the solvent's freezing point. The depression is a colligative property — it depends on the number of solute particles, not their identity. NCERT Class 12 Chemistry Chapter 1 (page 20) gives the relationship:
ΔT_f = K_f × m
where K_f is the cryoscopic constant of the solvent (water: 1.86 K·kg/mol) and m is molality (moles of solute per kg of solvent — not per kg of solution).
For electrolytes, each formula unit dissociates into ions, increasing the effective particle count. The corrected form is:
ΔT_f = i × K_f × m
where i is the Van't Hoff factor. NaCl → Na⁺ + Cl⁻ gives i ≈ 2. CaCl₂ → Ca²⁺ + 2 Cl⁻ gives i ≈ 3. Forgetting i gives you exactly half (or one-third) of the correct answer — and that value will be sitting in the options waiting for you.
Molar mass from ΔT_f. A common NEET pattern: you observe a freezing-point depression, know K_f and the mass of solute, and back-calculate molar mass. Rearrange: M₂ = (K_f × w₂ × 1000) / (ΔT_f × w₁), where w₂ is mass of solute in grams and w₁ is mass of solvent in grams. For electrolytes, replace K_f with i × K_f (or equivalently divide the calculated M₂ by i).
Watch-out: molality uses mass of solvent, not mass of solution. If the problem gives total solution mass, subtract the solute mass first.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
The freezing-point depression of a solution is a colligative property because it depends on:
The SI unit of the cryoscopic constant K_f is:
Which of the following aqueous solutions will show the greatest depression in freezing point? (Assume complete dissociation and equal molality for all.)
5.85 g of NaCl (molar mass = 58.5 g/mol) is dissolved in 500 g of water. If K_f for water is 1.86 K·kg/mol and NaCl dissociates completely, the depression in freezing point is:
3.0 g of a non-electrolyte solute is dissolved in 100 g of water. The freezing point of the solution is found to be −0.93 °C. If K_f for water is 1.86 K·kg/mol, the molar mass of the solute is:
The freezing point of a 0.05 m aqueous solution of K₂SO₄ is (assume complete dissociation, K_f = 1.86 K·kg/mol):
0.6 g of urea (molar mass 60 g/mol) and 0.585 g of NaCl (molar mass 58.5 g/mol) are dissolved together in 200 g of water. If K_f = 1.86 K·kg/mol and NaCl dissociates completely, the freezing-point depression is:
An aqueous solution of a substance X freezes at −0.558 °C. When 1.0 g of X is dissolved in 100 g of water, K_f = 1.86 K·kg/mol. The solution is found to have Van't Hoff factor i = 2. The molar mass of X (as an undissociated formula unit) is:
Given
- 11.1 g of CaCl₂ (molar mass = 111 g/mol) dissolved in 500 g of water - K_f for water = 1.86 K·kg/mol - CaCl₂ dissociates completely
Required
Depression of freezing point, ΔT_f
Concept
Freezing-point depression is a colligative property. For an electrolyte, the effective particle count is higher than the formula-unit count, so we must include the Van't Hoff factor *i*. CaCl₂ → Ca²⁺ + 2 Cl⁻ produces 3 ions per formula unit, so i = 3 (NCERT Class 12 Chemistry Chapter 1, page 20).
Formula
ΔT_f = i × K_f × m, where m = (moles of solute) / (kg of solvent)
Substitution
- Moles of CaCl₂ = 11.1 g / 111 g/mol = 0.1 mol - Mass of solvent = 500 g = 0.500 kg - m = 0.1 / 0.500 = 0.2 mol/kg - ΔT_f = 3 × 1.86 × 0.2
Calculation
ΔT_f = 3 × 1.86 × 0.2 = 3 × 0.372 = 1.116 K Note on exact values: the integer 3 (ion count) and the division 11.1/111 = 0.1 (exact by construction of the problem) are counting/exact quantities and do not limit significant figures. K_f = 1.86 (3 sig figs) governs precision.
Final answer
ΔT_f = 1.12 K (3 significant figures, governed by K_f = 1.86) Freezing point of solution = 0 − 1.12 = −1.12 °C
Common trap
Without the Van't Hoff factor: ΔT_f = 1.86 × 0.2 = 0.372 K — exactly one-third of the correct answer. This is the value NTA places as a distractor. If your answer is suspiciously small for an ionic compound, check whether you included *i*.
Similar NEET-style question
*What is the freezing point of a solution containing 5.85 g of NaCl (M = 58.5 g/mol) in 250 g of water? (K_f = 1.86 K·kg/mol, complete dissociation)* Approach: moles = 0.1, m = 0.1/0.250 = 0.4 mol/kg, i = 2 for NaCl. ΔT_f = 2 × 1.86 × 0.4 = 1.488 K. Freezing point = −1.49 °C. ---
ΔT_f = K_f × m, where K_f is cryoscopic constant (water: 1.86 K·kg/mol). Used to determine molar mass of solute.
-- NCERT Class 12 Chemistry, Ch. 1, p. 20Molal concentration: moles of solute per kg of solvent. Temperature-independent.
| Symbol | Quantity | SI Unit |
|---|---|---|
| m | molality | mol/kg |
| n | moles solute | mol |
Molar concentration: moles of solute per litre of solution.
| Symbol | Quantity | SI Unit |
|---|---|---|
| M | molarity | mol/L |
| n | moles solute | mol |
| V | solution volume | L |
Solute raises boiling point. K_b is ebullioscopic constant of solvent (water: 0.52 K kg/mol).
| Symbol | Quantity | SI Unit |
|---|---|---|
| ΔT_b | BP elevation | K |
| K_b | ebullioscopic constant | K kg/mol |
| m | molality | mol/kg |
Solute lowers freezing point. K_f is cryoscopic constant of solvent (water: 1.86 K kg/mol). Used for molar mass determination.
| Symbol | Quantity | SI Unit |
|---|---|---|
| ΔT_f | FP depression | K |
| K_f | cryoscopic constant | K kg/mol |
| m | molality | mol/kg |
Pressure required to prevent osmosis. C in mol/L; T in K. Used for high-molar-mass biomolecules.
| Symbol | Quantity | SI Unit |
|---|---|---|
| π | osmotic pressure | Pa |
| C | molarity | mol/L |
| R | gas constant | J/mol/K |
| T | temp | K |
Total vapor pressure of ideal solution = sum of mole-fraction-weighted vapor pressures of components.
| Symbol | Quantity | SI Unit |
|---|---|---|
| p | total vapor pressure | Pa |
| p_i° | pure component vp | Pa |
| x_i | mole fraction | - |
For non-volatile solute: relative lowering of VP equals mole fraction of solute.
| Symbol | Quantity | SI Unit |
|---|---|---|
| p | solution vp | Pa |
| p° | pure solvent vp | Pa |
| x_solute | mole fraction | - |
Correction factor for electrolytes. NaCl: i≈2; CaCl₂: i≈3. Multiply colligative formula by i.
| Symbol | Quantity | SI Unit |
|---|---|---|
| i | Van't Hoff factor | - |
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Similar Terms
Student uses mass fraction (w₁/total mass) where mole fraction (n₁/total moles) is required.
Question gives masses or molar masses and asks about Raoult's law or vapor pressure.
Raoult's law uses MOLE fractions, not mass fractions. Convert mass to moles first using molar mass.
Category: Similar Terms
Student uses non-electrolyte colligative formula for ionic compound. NaCl: i ≈ 2; CaCl₂: i ≈ 3.
Question gives an ionic compound (NaCl, CaCl₂, K₂SO₄) and asks for colligative property.
For electrolytes, multiply colligative formula by Van't Hoff factor i. NaCl → Na⁺ + Cl⁻ (i=2). CaCl₂ → Ca²⁺ + 2Cl⁻ (i=3). K₂SO₄ → 2K⁺ + SO₄²⁻ (i=3).
Root cause: formula misuse
Convert mass to moles first using molar mass. Raoult uses MOLE fractions.
Root cause: formula misuse
For NaCl i ≈ 2, CaCl₂ i ≈ 3, K₂SO₄ i ≈ 3. Multiply colligative formulas by i.
9 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
Which of the following aqueous solution will exhibit highest boiling point?
The IUPAC name of an element with atomic number 119 is
The structures of beryllium chloride in solid state and vapour phase, are :
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
forgets i factor electrolytes
Uses non-electrolyte formula for ionic solute
forgets conversion of units
Mixes Pa with atm; L with m^3
uses mass fractions not mole
Substitutes mass fraction for x
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