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Solutions appeared 45 times across 3 years — 5.2% of Chemistry. This question is from Colligative Properties - Freezing Point Depression.

Year 2026 2025 2024 Total
Questions 14 20 11 45

What is the freezing point depression constant of a solvent, 50g of which contain 1g non-volatile solute (molar mass 256g mol⁻¹ ) and the decrease in freezing point is 0.40K ?

Solution & Explanation

Related Formula

Freezing point depression relationship:

Δ Tf = Kf · m

where m is the molality defined as:

m = moles of solutemass of solvent in kg
Step 1: Compute Molality

Moles of non-volatile solute:

moles = 1 g256 g mol⁻¹

Mass of solvent in kg:

mass = 50 g = 50 × 10⁻³ kg

Therefore, molality values map to:

m = 1256 × 50 × 10⁻³ = (1000)/(12800) = (5)/(64) mol kg⁻¹
Step 2: Calculate Kf

Substituting values into the core formula:

0.40 = Kf · ((5)/(64)) Kf = (0.40 × 64)/(5) = 0.08 × 64 = 5.12 K kg mol⁻¹
Pattern Recognition

Sees: Direct calculation of cryogenic context constant (Kf). Shortcut: Isolate Kf = Δ Tf · M · Wsolvent1000 · wsolute. Substituting instantly returns 5.12.

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Q49 jee_main_2025_02_april_evening Elevation of Boiling Point and Molar Mass Determination
When 1~g each of compounds AB and AB₂ are dissolved in 15~g of water separately, they increased the boiling point of water by 2.7~K and 1.5~K respectively. The atomic mass of A (in amu) is × 10⁻¹ (Nearest integer) (Given : Molal boiling point elevation constant is 0.5~ K~kg~mol⁻¹)
Numerical Answer. Answer: 25 to 25

Solution

Related Formula
Δ Tb = Kb · m = Kb · ( wsoluteMsolute · 1000wsolvent )
Core Logic

Both dissolved compounds are non-electrolytes (van 't Hoff factor i = 1). We calculate the molar masses of AB and AB₂ individually, then solve for the individual atomic masses of elements A and B.

Step 1: Determine Molar Mass of AB

Given Δ Tb = 2.7~K, wsolute = 1~g, wsolvent = 15~g, and Kb = 0.5~ K~kg~mol⁻¹:

2.7 = 0.5 × 1MAB × (1000)/(15) MAB = (0.5 × 1000)/(15 × 2.7) = (500)/(40.5) ≈ 12.3457~ g~mol⁻¹
Step 2: Determine Molar Mass of AB_2

Given Δ Tb = 1.5~K, wsolute = 1~g, wsolvent = 15~g, and Kb = 0.5:

1.5 = 0.5 × 1MAB₂ × (1000)/(15) MAB₂ = (0.5 × 1000)/(15 × 1.5) = (500)/(22.5) ≈ 22.2222~ g~mol⁻¹
Step 3: Solve for Atomic Mass of A

Let the atomic masses of elements A and B be a and b respectively:

a + b = 12.3457 --- (1) a + 2b = 22.2222 --- (2)

Subtracting equation (1) from (2):

b = 22.2222 - 12.3457 = 9.8765~amu

Substituting b back into equation (1):

a = 12.3457 - 9.8765 = 2.4692~amu

Expressing a in the requested format (× 10⁻¹):

a = 24.692 × 10⁻¹ ≈ 25 × 10⁻¹
Pattern Recognition

Mathematical consistency checks: Since AB₂ has more atoms than AB of identical constituent mass, its molar mass should be higher, leading to a smaller elevation of boiling point for the same mass dissolved, which perfectly matches our 2.7~K arrow 1.5~K change.

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Q jee_main_2025_02_april_morning Henry's Law Constant and Temperature Dependance
Which of the following graph correctly represents the plots of KH at 1 bar gases in water versus temperature?
  • A.
  • B.
  • C.
  • D.

Solution

Related Formula

Henry's Law formula connects partial pressure to solubility component:

p = KH · x
Core Logic

As temperature increases, gas dissolution is typically exothermic, meaning solubility initially drops, causing the Henry's constant KH to curve upward dynamically before varying at extreme points. For standard non-reactive noble/molecular gases at regular ranges, the magnitude order follows:

KH(He) > KH(N₂) > KH(CH₄)
Step 1: Selection

Graph (4) illustrates the correct relative order and curved profile properly across the given temperature frame.

Pattern Recognition

Higher KH value implies lower solubility of that gas at a given pressure. Helium is notoriously insoluble in water compared to organic or polarizable molecules like methane, hence its plot line must live at the top.

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Q32 jee_main_2025_02_april_morning Raoult's Law and Vapour Pressure
A solution is made by mixing one mole of volatile liquid A with 3 moles of volatile liquid B. The vapour pressure of pure A is 200 ~mmHg and that of the solution is 500 ~mmHg. The vapour pressure of pure B and the least volatile component of the solution, respectively, are :
  • A. (1) 1400 mmHg, A
  • B. (2) 1400 mmHg, B
  • C. (3) 600 mmHg, B
  • D. (4) 600 mmHg, A

Solution

Related Formula

Raoult's Law for a multi-component solution mixtures:

PS = PA⁰ · XA + PB⁰ · XB
Core Logic

Let's determine the mole fractions first based on the input molar amounts:

XA = (1)/(1+3) = (1)/(4), XB = (3)/(1+3) = (3)/(4)

Substitute the known properties into Raoult's equation block:

500 = 200 × (1)/(4) + PB⁰ × (3)/(4) 500 = 50 + PB⁰ × (3)/(4) 450 = PB⁰ × (3)/(4) PB⁰ = 600 ~mmHg

Comparing pure state components pressures: PA⁰ = 200 ~mmHg and PB⁰ = 600 ~mmHg. Lower vapor pressure indicates stronger intermolecular cohesion, making A the least volatile component.

Step 1: Finalization

Thus, the vapour pressure of pure B is 600~mmHg and the least volatile chemical is A.

Pattern Recognition

Volatility is directly proportional to pure vapor pressure (P⁰). Don't mix up 'least volatile' with 'lowest mole fraction'—always evaluate based solely on the isolated values of P⁰.

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Q49 jee_main_2025_07_april_morning Van't Hoff Factor
The percentage dissociation of a salt (MX₃) solution at given temperature (van't Hoff factor i = 2) is ______ %. (Nearest integer)
Numerical Answer. Answer: 33 to 33

Solution

Related Formula
i = 1 + (n - 1)α
Core Logic

For the salt MX₃:

MX₃ arrow M³⁺ + 3X^-
  • Number of ions formed per formula unit, n = 1 + 3 = 4.
  • Given i = 2, let's find the degree of dissociation (α):

i = 1 + (4 - 1)α 2 = 1 + 3α 3α = 1 α = (1)/(3) ≈ 0.3333

Percentage dissociation:

% dissociation = α × 100 = 33.33 % ≈ 33 %
Pattern Recognition

Shortcut: For MX₃ dissociating into 4 ions, α = (i - 1) / 3. Since i = 2, α = 1/3 = 33% directly.

Evaluation Rubric / Model Answer

Simple formula application verifying the degree of dissociation to obtain a precise 33 percent.

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Q33 jee_main_2025_08_april_evening Azeotropic Mixtures
Which of the following binary mixtures does not show the behaviour of minimum boiling azeotropes?
  • A. H₂O + CH₃COC₂H₅
  • B. C₆H₅OH + C₆H₅NH₂
  • C. CS₂ + CH₃COCH₃
  • D. CH₃OH + CHCl₃

Solution

Core Logic

Let's connect deviation behaviors to azeotropic styles:

  • Minimum Boiling Azeotropes: Formed by liquid binary solutions that display a strong positive deviation from Raoult's Law. In these mixtures, inter-molecular forces between components (A-B) are weaker than pure self-interactions (A-A or B-B).
  • Maximum Boiling Azeotropes: Formed by liquid binary mixtures showing a notable negative deviation from Raoult's Law. Here, new inter-molecular interactions (A-B) become significantly stronger.
  • Analyzing Phenol (C₆H₅OH) + Aniline (C₆H₅NH₂): The phenolic -OH proton forms strong intermolecular hydrogen bonds with the lone pair of the -NH₂ group of aniline. These new forces exceed the initial individual fluid bonds, lowering vapor pressure below ideal expectations (negative deviation) and creating a maximum boiling azeotrope.

Pattern Recognition

Phenol + Aniline, and Chloroform + Acetone are classic textbook models of strong negative deviation from Raoult's Law. Negative deviation explicitly pairs with maximum boiling azeotropes, standing out instantly against minimum boiling selections.

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