(p° - p)/p° = χ_solute (mole fraction of solute). Useful when solute is non-volatile, non-electrolyte.
-- NCERT Class 12 Chemistry, Ch. 1, p. 16Relative Lowering Vp
Lesson
The trap that costs marks on relative lowering of vapour pressure is straightforward: students substitute mass fractions where mole fractions are required.
When a non-volatile solute dissolves in a solvent, the vapour pressure of the solution drops below that of the pure solvent. Raoult's law for a non-volatile solute gives:
(p° − p) / p° = x_solute
where p° is the vapour pressure of the pure solvent, p is the vapour pressure of the solution, and x_solute is the mole fraction of the solute. The left side — (p° − p) / p° — is called the relative lowering of vapour pressure. It depends only on how many solute particles are present relative to total moles, not on the nature of the solute (for non-electrolytes in dilute solution). This makes it a colligative property.
NCERT Class 12 Chemistry Chapter 1, page 16 derives this directly from Raoult's law for the solvent: p = p°·x_solvent. Since x_solvent + x_solute = 1, subtracting gives (p° − p)/p° = x_solute.
The high-frequency trap: a problem gives you masses of solute and solvent plus their molar masses. You must convert masses to moles before computing x_solute. Plugging mass fractions (g solute / g total) into the formula yields a wrong answer that often appears as a distractor.
For a two-component system with n_solute moles of solute and n_solvent moles of solvent:
x_solute = n_solute / (n_solute + n_solvent)
Watch out: when the problem states "10 g of glucose (M = 180 g/mol) in 90 g of water (M = 18 g/mol)," the mole fraction of glucose is 0.0556/5.056 ≈ 0.011 — not 10/100 = 0.10. That ten-fold error is exactly what the wrong option exploits.
Practice MCQs
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
The relative lowering of vapour pressure of a solution is equal to:
Relative lowering of vapour pressure is a colligative property because it depends on:
Which of the following conditions must hold for (p° − p)/p° = x_solute to apply?
6.0 g of urea (M = 60 g/mol) is dissolved in 180 g of water (M = 18 g/mol). The relative lowering of vapour pressure of the solution is:
18 g of glucose (M = 180 g/mol) is dissolved in 178.2 g of water (M = 18 g/mol). If the vapour pressure of pure water at the given temperature is 23.8 mmHg, the vapour pressure of the solution is closest to:
Two solutions are prepared: (I) 3.0 g of urea (M = 60 g/mol) in 100 g of water, and (II) 3.0 g of glucose (M = 180 g/mol) in 100 g of water. Which solution has a greater relative lowering of vapour pressure?
A solution of a non-volatile solute in water has a relative lowering of vapour pressure of 0.020. If the molar mass of water is 18 g/mol, what is the approximate molality of the solution?
A solution contains 12.0 g of a non-volatile, non-electrolyte solute in 108 g of water (M = 18 g/mol). The relative lowering of vapour pressure is found to be 0.020. The molar mass of the solute is closest to:
Quick recall before you leave
Worked Example
Pattern: Raoult's law VP calculation — find the relative lowering and the solution's vapour pressure (P.CHE.U05.RAOULTS_LAW_VP).
- 1
Given
- Mass of glucose = 9.0 g, M_glucose = 180 g/mol - Mass of water = 162 g, M_water = 18 g/mol - p° (pure water at 25°C) = 23.8 mmHg - Glucose is a non-volatile, non-electrolyte solute
- 2
Required
(a) Relative lowering of vapour pressure, (p° − p)/p° (b) Vapour pressure of the solution, p
- 3
Concept
For a non-volatile solute, the relative lowering of vapour pressure equals the mole fraction of the solute: (p° − p)/p° = x_solute. This is derived from Raoult's law: p = p°·x_solvent, and x_solvent + x_solute = 1 (NCERT Class 12 Chemistry Chapter 1, page 16).
- 4
Formula
(p° − p)/p° = x_solute = n_solute / (n_solute + n_solvent)
- 5
Substitution
n_glucose = 9.0 / 180 = 0.050 mol n_water = 162 / 18 = 9.00 mol x_solute = 0.050 / (0.050 + 9.00) = 0.050 / 9.05
- 6
Calculation
x_solute = 0.050 / 9.05 = 5.52 × 10⁻³ Note on exact values: molar masses (180 g/mol, 18 g/mol) are defined molecular weights used as exact divisors; they do not limit significant figures. The given masses (9.0 g, 162 g) determine the precision — 2 significant figures from 9.0 g. (a) Relative lowering = 5.52 × 10⁻³ ≈ 5.5 × 10⁻³ (b) p = p° × (1 − x_solute) = 23.8 × (1 − 5.52 × 10⁻³) = 23.8 × 0.99448 = 23.67 mmHg
- 7
Final answer
(a) Relative lowering of vapour pressure = 5.5 × 10⁻³ (b) Vapour pressure of solution ≈ 23.7 mmHg
- 8
Common trap
If you use mass fraction instead of mole fraction: mass fraction of glucose = 9.0/(9.0 + 162) = 0.0526, which is nearly 10× the correct answer. This error leads to p ≈ 22.55 mmHg — a plausible-looking but wrong value that typically appears as a distractor.
- 9
Similar NEET-style question
5.0 g of a non-volatile, non-electrolyte solute (M = 100 g/mol) is dissolved in 90 g of water. If p° of water at the given temperature is 17.5 mmHg, find the vapour pressure of the solution. *(Answer: n_solute = 0.050 mol, n_water = 5.00 mol, x_solute = 0.050/5.05 = 9.9 × 10⁻³, p = 17.5 × 0.9901 ≈ 17.3 mmHg.)* ---
Before solving, remember these
Formulas
Molality
Molal concentration: moles of solute per kg of solvent. Temperature-independent.
| Symbol | Quantity | SI Unit |
|---|---|---|
| m | molality | mol/kg |
| n | moles solute | mol |
Valid when
- Mass of SOLVENT (not solution)
Molarity
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 |
Valid when
- Volume of SOLUTION not solvent
- Temperature dependent (volume changes with T)
Boiling-point elevation
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 |
Valid when
- Dilute solution
- Non-electrolyte
Freezing-point depression
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 |
Valid when
- Dilute solution
- Non-electrolyte (else multiply by i)
Osmotic pressure
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 |
Valid when
- Dilute solution
- Semipermeable membrane separating pure solvent from solution
Raoult's law
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 | - |
Valid when
- Ideal solution
- Both volatile
Relative lowering of VP
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 | - |
Valid when
- Non-volatile solute
- Dilute solution
- Non-electrolyte (else use i)
Van't Hoff factor
Correction factor for electrolytes. NaCl: i≈2; CaCl₂: i≈3. Multiply colligative formula by i.
| Symbol | Quantity | SI Unit |
|---|---|---|
| i | Van't Hoff factor | - |
Valid when
- Electrolyte solution
- Account for ion-pair association/dissociation
Exam Traps & Common Mistakes
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.
When it triggers
Question gives masses or molar masses and asks about Raoult's law or vapor pressure.
How to avoid
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.
When it triggers
Question gives an ionic compound (NaCl, CaCl₂, K₂SO₄) and asks for colligative property.
How to avoid
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
Correction
Convert mass to moles first using molar mass. Raoult uses MOLE fractions.
Root cause: formula misuse
Correction
For NaCl i ≈ 2, CaCl₂ i ≈ 3, K₂SO₄ i ≈ 3. Multiply colligative formulas by i.
Past Year Questions
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 :
How NEET usually asks this
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
Calculate ΔT_f or ΔT_b given molality. Or determine molar mass from observed colligative property.
Common distractors
forgets i factor electrolytes
Uses non-electrolyte formula for ionic solute
π = CRT. Find molar mass of solute from observed osmotic pressure.
Common distractors
forgets conversion of units
Mixes Pa with atm; L with m^3
Find total VP of ideal solution from mole fractions and pure-component VPs.
Common distractors
uses mass fractions not mole
Substitutes mass fraction for x
Sources
Test yourself on this topic with real past-paper questions:
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