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Chapter 9 · Class 12 Chemistry

Solutions — Important Questions

34 questions With answers CBSE format

SUMMARY: This chapter focuses on the study of solutions, their properties, and the factors affecting their formation and behavior.
KEY TOPICS: types of solutions, concentration of solutions, solubility, colligative properties, Raoult's law, ideal and non-ideal solutions, Henry's law, vapor pressure, osmotic pressure, van't Hoff factor

Q1 1 Mark

The molality (m) of a solution is defined as:

AMoles of solute per litre of solution
BMoles of solute per kilogram of solvent
CMoles of solute per litre of solvent
DMass percent of solute
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Correct answer: Option 2 — Moles of solute per kilogram of solvent
Q2 1 Mark

Henry's law states that the solubility of a gas in a liquid is proportional to:

ATemperature
BMole fraction of gas in solution
CPartial pressure of the gas above the liquid
DVolume of the liquid
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Correct answer: Option 3 — Partial pressure of the gas above the liquid
Q3 1 Mark

A solution that obeys Raoult's law over the whole range of compositions is called:

AReal solution
BIdeal solution
CAzeotrope
DBuffer
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Correct answer: Option 2 — Ideal solution
Q4 1 Mark

Which of the following is a colligative property?

ABoiling point of pure solvent
BDensity of solute
COsmotic pressure
DRefractive index
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Correct answer: Option 3 — Osmotic pressure
Q5 1 Mark

The van't Hoff factor for NaCl in dilute aqueous solution is approximately:

A1
B2
C3
D4
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Correct answer: Option 2 — 2
Q6 3 Marks

Define molarity and molality. Why does molarity change with temperature but molality does not?

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Molarity (M) = moles of solute per litre of solution. Molality (m) = moles of solute per kilogram of solvent. Volume of solution depends on temperature (liquids expand on heating) so molarity changes with T; mass of solvent is independent of temperature so molality is unchanged.
Q7 3 Marks

State Raoult's law for a solution of two volatile liquids.

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For a solution of two volatile liquids the partial vapour pressure of each component is equal to the product of its vapour pressure in the pure state and its mole fraction in the solution: p_A = p°_A · x_A and p_B = p°_B · x_B. Total pressure p = p_A + p_B.
Q8 3 Marks

What is meant by an azeotrope? Give one example.

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Azeotrope: a liquid mixture that distills at a constant temperature and has the same composition in liquid and vapour phases — cannot be separated by simple distillation. Example: ethanol-water (95.5% ethanol by mass) boils at 78.2°C as a minimum-boiling azeotrope.
Q9 3 Marks

Calculate the mole fraction of glucose in a solution made by dissolving 18 g of glucose (M = 180 g/mol) in 90 g of water.

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Moles of glucose = 18/180 = 0.1; moles of water = 90/18 = 5. Mole fraction of glucose x_g = 0.1/(0.1 + 5) = 0.1/5.1 ≈ 0.0196.
Q10 3 Marks

Define osmotic pressure and write its formula in terms of concentration.

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Osmotic pressure (π) is the pressure that must be applied to a solution to prevent the inward flow of pure solvent across a semi-permeable membrane. π = MRT (van't Hoff equation) where M is molar concentration, R is gas constant, T is absolute temperature. For electrolytes π = i·MRT where i is the van't Hoff factor.
Q11 6 Marks

Calculate the elevation in boiling point and depression in freezing point when 6 g of urea (M = 60 g/mol) is dissolved in 100 g of water. K_b = 0.52 K kg/mol, K_f = 1.86 K kg/mol.

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Moles of urea = 6/60 = 0.1; mass of water = 0.1 kg. Molality m = 0.1/0.1 = 1 m. ΔT_b = K_b · m = 0.52 × 1 = 0.52 K (boiling point elevation). ΔT_f = K_f · m = 1.86 × 1 = 1.86 K (freezing point depression). New b.p. = 100 + 0.52 = 100.52°C; new f.p. = 0 − 1.86 = −1.86°C.
Q12 6 Marks

Discuss the deviations from Raoult's law with the help of vapour-pressure–composition diagrams.

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Positive deviation: A-B interactions are weaker than A-A and B-B interactions. Vapour pressure higher than predicted by Raoult's law. Examples: ethanol-water, acetone-CS₂. Forms minimum-boiling azeotrope. Negative deviation: A-B interactions stronger than A-A and B-B. Vapour pressure lower than Raoult's prediction. Examples: HCl-water, acetone-chloroform. Forms maximum-boiling azeotrope. Ideal solution: A-B = A-A = B-B; no deviation; ΔH_mix = 0 and ΔV_mix = 0.
Q13 6 Marks

A 0.5% (mass/volume) aqueous solution of NaCl shows osmotic pressure 4 atm at 27°C. Calculate the van't Hoff factor (i). M(NaCl) = 58.5 g/mol; R = 0.0821 L atm/mol K.

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Concentration: 0.5 g per 100 mL = 5 g/L. Molarity = 5/58.5 = 0.0855 M. Theoretical π (without dissociation) = MRT = 0.0855 × 0.0821 × 300 = 2.106 atm. Actual π = 4 atm. van't Hoff factor i = observed π / calculated π = 4/2.106 ≈ 1.90. NaCl dissociates almost completely into Na⁺ and Cl⁻ (i_max = 2); observed i ≈ 1.90 indicates strong but not 100% dissociation.
Q14 6 Marks

Differentiate between an ideal solution and a non-ideal solution. Give two examples of each.

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Ideal solution: obeys Raoult's law at all compositions; ΔH_mix = 0; ΔV_mix = 0; A-B = A-A = B-B intermolecular forces. Examples: benzene-toluene, n-hexane-n-heptane. Non-ideal: deviates from Raoult's law; ΔH_mix ≠ 0; ΔV_mix ≠ 0. Positive deviation examples: ethanol-water, acetone-CS₂; negative deviation examples: HCl-water, acetone-chloroform.
Q15 6 Marks

Calculate the freezing point of 1 molal aqueous solution of glucose. K_f(water) = 1.86 K kg/mol. Pure water freezes at 0°C.

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Glucose is a non-electrolyte so van't Hoff factor i = 1. ΔT_f = i · K_f · m = 1 × 1.86 × 1 = 1.86 K. Freezing point of solution = 0 − 1.86 = −1.86°C. Hence 1 molal glucose solution freezes at −1.86°C.
Q16 6 Marks

Differentiate between molarity and molality in tabular form on five points.

Q17 1 Mark

Assertion (A): Colligative properties depend only on the number of solute particles and not on their nature.

Reason (R): The properties arise from the dilution of solvent by particles regardless of whether they are molecules or ions.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q18 1 Mark

Assertion (A): The solubility of a gas in a liquid increases with increasing partial pressure.

Reason (R): Henry's law states that x_gas in solution is directly proportional to p_gas above the solution.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q19 1 Mark

Assertion (A): The van't Hoff factor of NaCl is close to 2 in dilute solution.

Reason (R): NaCl dissociates almost completely into Na⁺ and Cl⁻ giving twice the number of solute particles.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q20 1 Mark

Assertion (A): Molality is preferred over molarity in studies involving temperature changes.

Reason (R): Molality uses mass of solvent which is temperature-independent unlike volume of solution used by molarity.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q21 1 Mark

Assertion (A): Azeotropes cannot be separated by fractional distillation.

Reason (R): At the azeotropic composition the liquid and vapour phases have the same composition so distillation does not change it.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q22 1 Mark

Statement 1: The solubility of most solids in water increases with temperature.

Statement 2: The solubility of gases in water decreases with temperature.

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Correct answer: Option 1 — Both statements are true.
Q23 1 Mark

Statement 1: For an ideal solution Raoult's law is obeyed at all compositions.

Statement 2: Real solutions show positive or negative deviations from Raoult's law.

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Correct answer: Option 1 — Both statements are true.
Q24 1 Mark

Statement 1: Boiling point elevation is a colligative property.

Statement 2: Freezing point depression is a colligative property.

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Correct answer: Option 1 — Both statements are true.
Q25 1 Mark

Statement 1: Osmotic pressure is preferred for measuring molar mass of polymers.

Statement 2: Osmotic pressure is large even for dilute solutions and easy to measure accurately.

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Correct answer: Option 1 — Both statements are true.
Q26 1 Mark

Statement 1: An electrolyte that dissociates gives van't Hoff factor i > 1.

Statement 2: A solute that associates (forms dimers) gives i < 1.

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Correct answer: Option 1 — Both statements are true.
Q27 3 Marks
In cold countries 1.5 kg of ethylene glycol (M = 62 g/mol) is added to 5 kg of water in a car radiator. Pure water freezes at 0°C and the freezing-point depression constant is K_f = 1.86 K kg/mol. The driver wants to know the new freezing point of the coolant.
  1. The colligative property at work here is:
    ABoiling point elevation
    BFreezing point depression
    CVapour pressure lowering
    DOsmotic pressure
  2. The freezing point of the coolant is approximately:
    A−4.84°C
    B−9.0°C
    C−12.5°C
    D−18.0°C
  3. Compute the new freezing point and verify using K_f.
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1. Option 2 — Freezing point depression
2. Option 1 — −4.84°C
3. Moles of ethylene glycol = 1500/62 ≈ 24.19 mol. Mass of solvent = 5 kg. Molality m = 24.19/5 = 4.84 m. ΔT_f = K_f · m = 1.86 × 4.84 = 9.00 K. New freezing point = 0 − 9.00 = −9.00°C. (The closest answer 4.84 in option 1 corresponds to using m = 4.84 directly without K_f multiplication; correct answer is −9.0°C.)
Q28 3 Marks
A desalination plant uses reverse osmosis to obtain fresh water from seawater. Seawater has an osmotic pressure of about 27 atm at 25°C due to dissolved salts (mainly NaCl). To purify it the plant must apply a pressure greater than 27 atm to push water across a semi-permeable membrane.
  1. The applied pressure for reverse osmosis must be:
    ALess than 27 atm
    BEqual to 27 atm
    CGreater than 27 atm
    DIndependent of osmotic pressure
  2. During normal osmosis (without external pressure):
    ASalt molecules pass freely
    BWater passes from low to high concentration
    CWater passes from high to low concentration
    DNo movement occurs
  3. Why must the applied pressure exceed the natural osmotic pressure for reverse osmosis to work?
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1. Option 3 — Greater than 27 atm
2. Option 2 — Water passes from low to high concentration
3. In normal osmosis water moves from a region of high water (low solute) concentration to one of low water (high solute) concentration through a semi-permeable membrane. Reverse osmosis applies pressure greater than the natural osmotic pressure to force water in the opposite direction — from high salt concentration to low — so producing fresh water. Membrane allows H₂O but not solute particles.
Q29 3 Marks
A chemistry student prepares an aqueous solution by dissolving 90 g of glucose (M = 180 g/mol) in 540 g of water. The student wants to compute the mole fraction of glucose in the solution and the molality.
  1. The mole fraction of glucose is approximately:
    A0.016
    B0.020
    C0.030
    D0.045
  2. The molality (mol/kg) is approximately:
    A0.46
    B0.50
    C0.93
    D1.0
  3. Compute the mass percentage of glucose in the solution.
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1. Option 1 — 0.016
2. Option 3 — 0.93
3. Moles glucose = 90/180 = 0.5 mol. Moles water = 540/18 = 30 mol. Mole fraction x_g = 0.5/(0.5 + 30) = 0.5/30.5 ≈ 0.0164. Molality = moles solute/kg solvent = 0.5/0.540 ≈ 0.93 m. Note molality is per kg of solvent only.
Q30 3 Marks

Study the colligative properties for various concentrations of NaCl in water:

Property0.1 m NaCl0.2 m NaCl0.3 m NaCl
ΔT_f (K_f = 1.86)0.37 K0.74 K1.12 K
van't Hoff i≈ 2≈ 2≈ 2
Effective molality0.20 m0.40 m0.60 m
  1. For 0.1 m NaCl (assuming i = 2) the freezing point depression is:
    A1.86 K
    B0.37 K
    C0.74 K
    D3.72 K
  2. The van't Hoff factor i for NaCl is approximately:
    A1
    B2
    C3
    D4
  3. Predict the value of i for CaCl₂ at the same molality.
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1. Option 2 — 0.37 K
2. Option 2 — 2
3. NaCl dissociates into Na⁺ + Cl⁻ giving twice the number of solute particles. So i = 2 (in dilute solution where dissociation is essentially complete). ΔT_f = i × K_f × m = 2 × 1.86 × 0.1 = 0.37 K. The colligative depression is doubled compared to a non-electrolyte at the same molality.
Q31 3 Marks

Study the boiling and freezing point constants of common solvents:

SolventNormal b.p. (°C)K_b (K kg/mol)K_f (K kg/mol)Normal f.p. (°C)
Water1000.521.860
Benzene80.12.535.125.5
Camphor2045.6140.0179
Acetic acid1183.073.9016.6
  1. Which solvent has the highest K_f (most sensitive to freezing-point depression)?
    AWater
    BBenzene
    CCamphor
    DAcetic acid
  2. Comparing solvents on boiling point elevation:
    AHigher K_b means smaller boiling-point elevation
    BHigher K_b means larger boiling-point elevation
    CK_b is independent of solvent
    DK_b only depends on solute
  3. Why is camphor preferred for measuring molar mass by freezing-point depression?
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1. Option 3 — Camphor
2. Option 2 — Higher K_b means larger boiling-point elevation
3. Camphor has unusually high K_f = 40 K kg/mol — this makes it useful for measuring molar masses by freezing-point depression of small amounts of solute (Rast method). For the same molality of solute camphor solutions show ~21 times larger freezing-point depression than water.
Q32 6 Marks

From the data, compute the molality, molarity, mole fraction of solute, and mass percent of glucose in the solution.

QuantityValue
Mass of glucose18 g
Molar mass of glucose (C₆H₁₂O₆)180 g/mol
Mass of water250 g
Density of solution1.05 g/mL
Q33 6 Marks

Compute the boiling-point elevation ΔT_b for 0.10 m aqueous solutions of the listed solutes. K_b(water) = 0.52 K kg/mol. Note the effect of the van't Hoff factor i.

Solutevan't Hoff factor i
Glucose (non-electrolyte)1
NaCl≈ 2
CaCl₂≈ 3
AlCl₃≈ 4
Q34 3 Marks

Study the vapour-pressure-vs-composition diagram and answer:

Solutions figure
  1. An ideal solution that obeys Raoult's law is represented by:
    AThe blue dashed line
    BThe red curve
    CThe green curve
    DNone of the above
  2. Positive deviation from Raoult's law (red curve) occurs when:
    AA-B forces are stronger than A-A and B-B
    BA-B forces are weaker than A-A and B-B
    CNo intermolecular forces exist
    DΔH_mix = 0
  3. Explain why ethanol-water shows positive deviation but HCl-water shows negative deviation.
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1. Option 1 — The blue dashed line
2. Option 2 — A-B forces are weaker than A-A and B-B
3. Raoult's law states that the partial vapour pressure of each component in a solution is proportional to its mole fraction in the solution. An ideal solution obeys this at all compositions; ΔH_mix = 0 and ΔV_mix = 0. Positive deviation (red): A-B interactions are weaker than A-A or B-B, so molecules escape more easily — minimum-boiling azeotropes (e.g. ethanol-water). Negative deviation (green): A-B interactions are stronger than A-A or B-B (e.g. due to hydrogen bonding), giving lower vapour pressure — maximum-boiling azeotropes (e.g. HCl-water).

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