Solutions Questions
Solutions Questions
a) Refractive index
b) Boiling point
c) Osmotic pressure
d) Viscosity
Answer: c
Q3. The molality of a solution containing 5.8 g NaCl in 500 g water is:
a) 0.1 m
b) 0.2 m
c) 0.4 m
d) 1.0 m
Answer: b
Q4. Which of the following solutions will have the lowest freezing point?
a) 0.1 M NaCl
b) 0.1 M Glucose
c) 0.1 M CaCl₂
d) 0.1 M Urea
Answer: c
Q7. Which of the following has maximum van’t Hoff factor (i)?
a) NaCl
b) K₂SO₄
c) Glucose
d) AlCl₃
Answer: d
a) atm
b) mol L⁻¹
c) mol kg⁻¹
d) atm mol⁻¹
Answer: a
a) Osmotic pressure
b) Elevation in boiling point
c) Freezing point depression
d) pH
Answer: d
Q33. If a solution has two volatile components, total vapour pressure is:
a) Sum of partial pressures
b) Average of partial pressures
c) Always less than both
d) Independent of mole fraction
Answer: a
Q44. Which colligative property is preferred for molar mass determination of biomolecules?
a) Freezing point depression
b) Boiling point elevation
c) Vapour pressure lowering
d) Osmotic pressure
Answer: d
a) Gain water
b) Swell
c) Shrink
d) Burst
Answer: c
Q54. Henry’s law constant for a gas is high. Its solubility is:
a) Low
b) High
c) Infinite
d) Zero
Answer: a
Q63. Which of the following shows negative deviation from Raoult’s law?
a) Acetone + Water
b) Chloroform + Acetone
c) Ethanol + Methanol
d) Benzene + Toluene
Answer: b
Q65. When two liquids are completely miscible and obey Raoult’s law, the solution is:
a) Ideal
b) Azeotropic
c) Non-ideal
d) Heterogeneous
Answer: a
Q66. The boiling point of pure solvent is 373 K. In presence of non-volatile solute, it becomes:
a) 373 K
b) >373 K
c) <373 K
d) 0 K
Answer: b
Q68. When vapour pressure of solution is lower than pure solvent, it shows:
a) Boiling point depression
b) Boiling point elevation
c) No change
d) Decomposition
Answer: b
Q76. Van’t Hoff factor becomes less than expected when solute:
a) Ionizes
b) Associates
c) Dissolves
d) Crystallizes
Answer: b
Q84. Van’t Hoff factor for Na₂SO₄ assuming 100% dissociation is:
a) 1
b) 2
c) 3
d) 4
Answer: c
Q86. What is the ideal value of i (van’t Hoff factor) for 1 M sucrose?
a) 0
b) 1
c) 2
d) 3
Answer: b
Q87. Which of the following shows positive deviation from Raoult’s law?
a) Acetone + Water
b) Benzene + Toluene
c) HNO₃ + Water
d) Chloroform + Acetone
Answer: a
Q95. Which of the following liquids pair is most likely to form a maximum boiling azeotrope?
a) Acetone + CS₂
b) HNO₃ + H₂O
c) Ethanol + Water
d) Chloroform + Acetone
Answer: b
Q101. Calculate the molality of a solution prepared by dissolving 5 g of NaOH (M = 40 g/mol) in 250 g of
water.
Answer:
Moles of NaOH = 5/40 = 0.125 mol
Mass of solvent (kg) = 250/1000 = 0.25 kg
Molality = 0.125 / 0.25 = 0.5 mol/kg
Q102. Calculate the mole fraction of glucose in a solution containing 180 g of glucose (M = 180 g/mol) in 900
g of water.
Answer:
Moles of glucose = 180/180 = 1 mol
Moles of water = 900/18 = 50 mol
Mole fraction of glucose = 1 / (1 + 50) = 0.0196
Q103. A 1 molal solution of a non-volatile solute is prepared in water. Calculate the depression in freezing
point. (Kf = 1.86 K·kg/mol)
Answer:
ΔTf = i × Kf × m = 1 × 1.86 × 1 = 1.86 K
Q104. A solution of urea (M = 60 g/mol) containing 3 g in 100 g of water. Calculate the lowering of vapour
pressure if vapour pressure of pure water is 25 mmHg.
Answer:
Moles of urea = 3/60 = 0.05 mol
Moles of water = 100/18 = 5.56 mol
Mole fraction of solute = 0.05 / (0.05 + 5.56) ≈ 0.0089
Relative lowering = 0.0089
Lowering = 25 × 0.0089 = 0.2225 mmHg
Q105. Calculate osmotic pressure of 0.2 M glucose solution at 27°C. (R = 0.0821 L·atm/mol·K)
Answer:
T = 273 + 27 = 300 K
π = CRT = 0.2 × 0.0821 × 300 = 4.926 atm
Q106. Find molar mass of solute if 2 g of it is dissolved in 100 g benzene (Kf = 5.12) and freezing point is
lowered by 0.64°C.
Answer:
Molality = ΔTf / Kf = 0.64 / 5.12 = 0.125 m
Mol of solute = molality × mass of solvent (kg) = 0.125 × 0.1 = 0.0125 mol
Molar mass = 2 / 0.0125 = 160 g/mol
Q107. A solution is prepared by dissolving 6 g of urea (M = 60 g/mol) in 90 g of water. Calculate the relative
lowering of vapour pressure.
Answer:
Moles of urea = 6 / 60 = 0.1 mol
Moles of water = 90 / 18 = 5 mol
Relative lowering = 0.1 / (0.1 + 5) = 0.0196
Q108. Calculate mass of NaCl (M = 58.5 g/mol) required to be dissolved in 500 g of water to lower freezing
point by 3.72°C. (Kf = 1.86)
Answer:
ΔTf = iKf m = 2 × 1.86 × m = 3.72
m = 3.72 / (2 × 1.86) = 1 mol/kg
Mol = 1 × 0.5 = 0.5 mol
Mass = 0.5 × 58.5 = 29.25 g
Q109. Calculate vapour pressure of water in a solution of 18 g glucose (M = 180 g/mol) in 180 g water.
(Vapour pressure of water = 760 mmHg)
Answer:
Moles glucose = 0.1 mol; Moles water = 10 mol
Mole fraction of water = 10 / (10 + 0.1) = 0.9901
Vapour pressure = 760 × 0.9901 = 752.47 mmHg
Q110. Calculate molar mass of solute when 1 g of it in 100 g of water causes osmotic pressure of 0.3 atm at
27°C.
Answer:
π = CRT → 0.3 = (1/M) × (1000/1000) × 0.0821 × 300
M = (1 × 0.0821 × 300) / 0.3 = 82.1 g/mol
Q111. Calculate boiling point of 0.5 molal KCl solution. (Kb = 0.52 K·kg/mol, water b.p. = 373 K)
Answer:
i = 2 (for KCl), ΔTb = iKb m = 2 × 0.52 × 0.5 = 0.52 K
Boiling point = 373 + 0.52 = 373.52 K
Q113. What is the freezing point of 0.1 molal solution of glucose in water? (Kf = 1.86)
Answer:
ΔTf = 1.86 × 0.1 = 0.186 K
Freezing point = 273 - 0.186 = 272.814 K
Q116. A solution shows 2 atm osmotic pressure at 300 K. Calculate concentration of solute.
Answer:
π = CRT → C = π / (RT) = 2 / (0.0821 × 300) = 0.0812 M
Q118. 50 g of ethylene glycol (M = 62) is dissolved in 200 g of water. Calculate freezing point depression.
Answer:
Mol = 50 / 62 = 0.806 mol
Molality = 0.806 / 0.2 = 4.03 m
ΔTf = 1.86 × 4.03 = 7.49 K
Q119. Calculate molar mass if 0.5 g of solute gives osmotic pressure of 1 atm in 100 mL at 298 K.
Answer:
π = CRT → 1 = (0.5/M) × (1) × 0.0821 × 298
M = 0.5 × 0.0821 × 298 = 12.24 g/mol
Q120. Boiling point elevation is 0.52°C for 1 molal solution. What is Kb?
Answer:
ΔTb = Kb × m → Kb = 0.52 / 1 = 0.52 K·kg/mol
Q121. 3.6 g of acetic acid (CH₃COOH, M = 60 g/mol) is dissolved in 100 g of benzene. Calculate molality.
Answer:
Mol = 3.6 / 60 = 0.06 mol
Mass solvent = 0.1 kg
Molality = 0.06 / 0.1 = 0.6 mol/kg
Q124. A 0.25 molal solution of a non-electrolyte is prepared in water. Calculate its freezing point.
Answer:
ΔTf = 1.86 × 0.25 = 0.465
Freezing point = 273 - 0.465 = 272.535 K
Q125. Calculate the mass of glucose (M = 180 g/mol) needed to make 500 mL of 0.5 M solution
Answer:
Mol = M × V = 0.5 × 0.5 = 0.25 mol
Mass = 0.25 × 180 = 45 g
Q127. Calculate vapour pressure of water in solution with 18 g glucose in 180 g water. (P° = 25 mmHg)
Answer:
Moles glucose = 0.1 mol; Moles water = 10 mol
Mole fraction of water = 10 / (10 + 0.1) = 0.9901
p = 25 × 0.9901 = 24.75 mmHg
Q128. 9 g of solute in 100 g water depresses freezing point by 0.93°C. Kf = 1.86. Find molar mass.
Answer:
Molality = 0.93 / 1.86 = 0.5
Moles = 0.5 × 0.1 = 0.05 mol
Molar mass = 9 / 0.05 = 180 g/mol
Q131. Determine molar mass if osmotic pressure is 5 atm at 300 K for 1 g solute in 100 mL.
Answer:
π = CRT → 5 = (1/M) × 1 × 0.0821 × 300
M = (1 × 0.0821 × 300) / 5 = 4.926 g/mol
Q132. Calculate elevation in boiling point for 0.1 molal urea solution. (Kb = 0.52)
Answer:
ΔTb = 0.52 × 0.1 = 0.052 K
Q133. What is the freezing point of 1.5 molal urea in water? (Kf = 1.86)
Answer:
ΔTf = 1.5 × 1.86 = 2.79
Freezing point = 273 - 2.79 = 270.21 K
Q134. 2 g of unknown solute in 100 mL water gives osmotic pressure of 2.46 atm at 300 K. Find molar mass.
Answer:
π = CRT → 2.46 = (2/M) × 1 × 0.0821 × 300
M = (2 × 0.0821 × 300) / 2.46 = 20 g/mol
Q135. 0.01 molal NaCl solution has what osmotic pressure at 25°C? (i = 2)
Answer:
π = 2 × 0.01 × 0.0821 × 298 = 0.489 atm
Q136. Calculate molar mass of solute if 1.5 g in 250 mL has osmotic pressure of 2 atm at 300 K.
Answer:
π = CRT → 2 = (1.5/M) × 4 × 0.0821 × 300
M = (1.5 × 0.0821 × 4 × 300) / 2 = 73.89 g/mol
Q137. What mass of NaCl (i = 2) is needed to lower freezing point by 1.86°C of 1 kg water? (Kf = 1.86)
Answer:
ΔTf = iKf m → m = ΔTf / (iKf) = 1.86 / (2 × 1.86) = 0.5
Mol = 0.5 mol; Mass = 0.5 × 58.5 = 29.25 g
Q138. A 0.1 molal NaCl solution freezes at 271.88 K. What is Kf? (i = 2)
Answer:
ΔTf = 273 - 271.88 = 1.12
Kf = ΔTf / (i × m) = 1.12 / (2 × 0.1) = 5.6 K·kg/mol
Q139. 0.5 mol of glucose in 1.5 L solution at 298 K. Find osmotic pressure.
Answer:
π = (0.5 / 1.5) × 0.0821 × 298 = 8.15 atm
Q141. 2 molal KNO₃ solution, find elevation in boiling point (Kb = 0.52, i = 2)
Answer:
ΔTb = i × Kb × m = 2 × 0.52 × 2 = 2.08 K
Q142. Vapour pressure of water = 25 mmHg. What is vapour pressure of 0.2 molal glucose solution?
Answer:
Mole water = 55.56 mol; Mole glucose = 0.2
Mole fraction water ≈ 55.56 / (55.56 + 0.2) ≈ 0.9964
p = 25 × 0.9964 = 24.91 mmHg
Q143. What mass of ethylene glycol (M = 62) must be added to 1 kg water to decrease freezing point by
3.72°C? (Kf = 1.86)
Answer:
Molality = 3.72 / 1.86 = 2
Moles = 2; Mass = 2 × 62 = 124 g
Q146. What is the freezing point of solution containing 0.1 mol of Na₂SO₄ in 1 kg water? (Kf = 1.86, i = 3)
Answer:
ΔTf = i × Kf × m = 3 × 1.86 × 0.1 = 0.558
Freezing point = 273 - 0.558 = 272.442 K
Q147. 4 g urea in 100 g water gives osmotic pressure 1.23 atm at 27°C. Find molar mass.
Answer:
π = CRT → 1.23 = (4/M) × 0.0821 × 300
M = (4 × 0.0821 × 300) / 1.23 = 80 g/mol
Q148. Find freezing point of 0.1 molal CaCl₂ solution. (Kf = 1.86, i = 3)
Answer:
ΔTf = 3 × 1.86 × 0.1 = 0.558
Freezing point = 273 - 0.558 = 272.442 K
(Marking Scheme: A - Both Assertion and Reason are true, and Reason is the correct explanation; B - Both
true, but Reason is not the correct explanation; C - Assertion is true, Reason is false; D - Assertion is false,
Reason is true)
Q151.
Assertion: A solution shows a lower vapour pressure than the pure solvent.
Reason: Presence of solute decreases the escaping tendency of solvent molecules.
Answer: A
Q152.
Assertion: Molality is independent of temperature.
Reason: Molality is based on mass, which does not change with temperature.
Answer: A
Q153.
Assertion: Molarity of a solution changes with temperature.
Reason: Volume expands or contracts with temperature change.
Answer: A
Q154.
Assertion: Elevation in boiling point depends on the nature of solute.
Reason: Strong electrolytes ionise and produce more particles.
Answer: A
Q155.
Assertion: Glucose does not affect colligative properties as much as NaCl.
Reason: NaCl dissociates into ions, increasing particle number.
Answer: A
Q156.
Assertion: Boiling point of water increases on adding salt.
Reason: Addition of non-volatile solute lowers vapour pressure.
Answer: A
Q157.
Assertion: Freezing point depression is directly proportional to molality.
Reason: It is a colligative property and depends only on number of solute particles.
Answer: A
Q158.
Assertion: In ideal solutions, ΔHmixing = 0.
Reason: There are no intermolecular force changes in ideal mixing.
Answer: A
Q159.
Assertion: In a non-ideal solution, azeotrope formation can occur.
Reason: Azeotropes have either maximum or minimum boiling points.
Answer: A
Q160.
Assertion: Henry’s law constant increases with temperature.
Reason: Solubility of gas increases with temperature.
Answer: C
Q161.
Assertion: In case of hypertonic solution, water flows out of cell.
Reason: Osmosis drives solvent from lower to higher solute concentration.
Answer: A
Q162.
Assertion: Adding sugar to water lowers its vapour pressure.
Reason: Non-volatile solutes occupy surface area and reduce escaping tendency.
Answer: A
Q163.
Assertion: Van’t Hoff factor for Na₂SO₄ is 3.
Reason: It dissociates into 2Na⁺ and SO₄²⁻ ions.
Answer: A
Q164.
Assertion: 1 molal NaCl solution shows more freezing point depression than 1 molal glucose.
Reason: NaCl dissociates to produce more particles than glucose.
Answer: A
Q165.
Assertion: Reverse osmosis is used for water purification.
Reason: It applies pressure higher than osmotic pressure to force solvent across semipermeable membrane.
Answer: A
Q166.
Assertion: Colligative properties depend on amount, not type of solute.
Reason: Only number of solute particles in solution matters.
Answer: A
Q167.
Assertion: Elevation in boiling point is observed in electrolyte solutions.
Reason: Electrolytes increase number of solute particles.
Answer: A
Q168.
Assertion: For non-ideal solutions, Raoult’s law is not strictly applicable.
Reason: Deviations occur due to changes in intermolecular interactions.
Answer: A
Q169.
Assertion: NaCl is an ideal solute.
Reason: It dissociates completely in water.
Answer: B
Q170.
Assertion: Osmotic pressure increases with dilution.
Reason: Osmotic pressure is directly proportional to solute concentration.
Answer: D
Q171.
Assertion: A 0.1 molal BaCl₂ solution will have more freezing point depression than NaCl.
Reason: BaCl₂ gives three ions per formula unit.
Answer: A
Q172.
Assertion: Molarity is affected by temperature, molality is not.
Reason: Molarity depends on volume which changes with temperature.
Answer: A
Q173.
Assertion: Vapour pressure of water decreases when common salt is added.
Reason: Salt particles block water molecules from escaping into vapour phase.
Answer: A
Q174.
Assertion: Lowering of vapour pressure is proportional to mole fraction of solute.
Reason: According to Raoult’s law, vapour pressure lowers linearly with addition of solute.
Answer: A
Q175.
Assertion: The freezing point of solution is always lower than that of pure solvent.
Reason: Solute particles obstruct crystal formation during freezing.
Answer: A
Q176.
Assertion: Presence of solute increases boiling point of solvent.
Reason: It raises the temperature required to equal atmospheric pressure.
Answer: A
Q177.
Assertion: Osmosis is a spontaneous process.
Reason: It occurs from lower to higher solute concentration naturally.
Answer: A
Q178.
Assertion: Azeotropes show constant boiling composition.
Reason: Their liquid and vapour phases have same composition.
Answer: A
Q179.
Assertion: Elevation in boiling point is more in ionic solutes.
Reason: Ionic compounds give more number of particles.
Answer: A
Q180.
Assertion: Molality and mole fraction remain unchanged with temperature.
Reason: They are mass-based concentration units.
Answer: A
Q181.
Assertion: For 1 molal urea and 1 molal NaCl, osmotic pressure is more for NaCl.
Reason: NaCl produces more number of particles.
Answer: A
Q182.
Assertion: Glucose solution has lower vapour pressure than water.
Reason: Solute particles reduce escaping tendency of water molecules.
Answer: A
Q183.
Assertion: Raoult’s law is applicable to ideal solutions only.
Reason: Ideal solutions follow linear relationship of pressure and composition.
Answer: A
Q184.
Assertion: Addition of volatile solute increases vapour pressure.
Reason: It increases the total number of particles in vapour phase.
Answer: A
Q185.
Assertion: Osmotic pressure is a colligative property.
Reason: It depends only on number of solute particles, not their nature.
Answer: A
Q186.
Assertion: Lowering of vapour pressure is a colligative property.
Reason: It depends on the nature of solute.
Answer: C
Q187.
Assertion: 0.1 molal NaCl solution shows greater osmotic pressure than 0.1 molal urea.
Reason: NaCl dissociates to give more particles.
Answer: A
Q188.
Assertion: Reverse osmosis removes ions and impurities.
Reason: Pressure higher than osmotic pressure forces water through membrane.
Answer: A
Q189.
Assertion: The osmotic pressure of a 1 M solution is greater at higher temperature.
Reason: Osmotic pressure is directly proportional to temperature.
Answer: A
Q190.
Assertion: Colligative properties are not affected by electrolyte dissociation.
Reason: Electrolyte dissociation increases number of solute particles.
Answer: C
Q191.
Assertion: Ethanol-water mixture shows positive deviation from Raoult’s law.
Reason: A–B interactions are weaker than A–A and B–B interactions.
Answer: A
Q192.
Assertion: NaCl shows greater effect on colligative properties than glucose.
Reason: Ionic compounds give multiple particles per formula unit.
Answer: A
Q193.
Assertion: Vapour pressure is independent of external pressure.
Reason: It depends on temperature and intermolecular forces.
Answer: A
Q194.
Assertion: Isotonic solutions have same osmotic pressure.
Reason: They have same solute concentration.
Answer: A
Q195.
Assertion: The freezing point of water decreases when alcohol is added.
Reason: Alcohol is volatile and adds more particles.
Answer: A
Q196.
Assertion: 1 mol of KCl produces more osmotic pressure than 1 mol of urea.
Reason: KCl dissociates into two ions.
Answer: A
Q197.
Assertion: A solution with higher concentration has higher boiling point.
Reason: More solute = more elevation in boiling point.
Answer: A
Q198.
Assertion: Solution with stronger intermolecular forces shows lower vapour pressure.
Reason: Molecules find it harder to escape from liquid phase.
Answer: A
Q199.
Assertion: The molarity of water is 55.5 M.
Reason: 1000 g water = 55.5 mol; Volume = 1 L
Answer: A
Q200.
Assertion: Presence of non-volatile solute increases boiling point.
Reason: It decreases vapour pressure, requiring more heat to boil.
Answer: A
Column I Column II
A. Molarity (M) 1. Moles of solute / Volume of solution (L)
B. Molality (m) 2. Moles of solute / Mass of solvent (kg)
C. Mole fraction (χ) 3. Moles of component / Total moles
D. Mass percent (%) 4. (Mass of solute / Mass of solution) × 100
Column I Column II
A. Elevation in boiling pt 1. ΔTb = i × Kb × m
B. Freezing point depression 2. ΔTf = i × Kf × m
Column I Column II
C. Osmotic pressure 3. π = i × C × R × T
D. Relative lowering of VP 4. ΔP / P° = χsolute
Q3. Match the type of solution with its deviation from Raoult’s law:
Column I Column II
A. Ideal solution 1. Obeys Raoult’s law
B. Positive deviation 2. A–B < A–A, B–B interaction
C. Negative deviation 3. A–B > A–A, B–B interaction
D. Azeotrope 4. Constant boiling mixture
Column I Column II
A. Boiling 1. Vapour pressure = atm pressure
B. Freezing 2. Solid-liquid equilibrium
C. Osmosis 3. Semipermeable membrane
D. Reverse osmosis 4. Pressure > π
Column I Column II
A. Molarity 1. Volume-based (temp. dependent)
B. Molality 2. Mass-based (temp. independent)
C. Mole fraction 3. Dimensionless
D. Normality 4. Gram equivalents / L
Column I Column II
A. Solvent 1. Medium in which solute dissolves
B. Solute 2. Substance dissolved
C. Solution 3. Homogeneous mixture
D. Solubility 4. Max amount of solute in solvent
Column I Column II
A. Electrolyte solute 1. i > 1
B. Non-electrolyte solute 2. i = 1
C. Strong electrolyte 3. Complete dissociation
D. Weak electrolyte 4. Partial dissociation
Column I Column II
A. Osmotic pressure 1. π
B. Boiling point elevation 2. ΔTb
C. Freezing point depression 3. ΔTf
D. Van’t Hoff factor 4. i
Q10. Match the type of colligative property with the observed phenomenon:
Column I Column II
A. Lowering of VP 1. Escaping tendency reduced
B. Elevation in BP 2. Needs higher temp to boil
C. Freezing point depression 3. Freezing delayed
D. Osmosis 4. Solvent flows via membrane
Column I Column II
A. Increase in temperature 1. Gas solubility decreases
B. Pressure increase 2. Gas solubility increases
C. Adding non-volatile solute 3. Vapour pressure lowers
Column I Column II
D. Salt to ice 4. Freezing point decreases
Column I Column II
A. Raoult’s Law 1. VP of solution is proportional to mole fraction
B. Henry’s Law 2. Gas solubility ∝ partial pressure
C. Van’t Hoff Eqn 3. Osmotic pressure formula
D. Dalton’s Law 4. Total pressure = sum of partial pressures
Column I Column II
A. Molarity 1. Changes with temperature
B. Molality 2. Independent of temperature
C. Mole fraction 3. Unitless
D. Mass percent 4. Expressed as %
Column I Column II
A. Freezing pt depression 1. De-icing roads
B. Boiling pt elevation 2. Antifreeze in radiators
C. Osmotic pressure 3. Determination of molar mass
D. VP lowering 4. Determines volatility
Column I Column II
A. π 1. Osmotic pressure
B. ΔTb 2. Boiling point elevation
C. ΔTf 3. Freezing point depression
D. i 4. Van’t Hoff factor
Column I Column II
A. Water 1. Solvent
B. Salt (NaCl) 2. Solute
C. Solution 3. Homogeneous mix
D. Saturated 4. Max solubility reached
Column I Column II
A. Pressure cooker 1. Elevated boiling point
B. Antifreeze 2. Lowered freezing point
C. Saline drip 3. Isotonic solution
D. Desalination 4. Reverse osmosis
Column I Column II
A. π = iCRT 1. atm
B. ΔTb = iKbm 2. Kelvin (K)
C. Molarity (mol/L) 3. mol/L
D. Molality (mol/kg) 4. mol/kg
Answer: A-1, B-2, C-3, D-4
Column I Column II
A. Osmotic pressure 1. Concentration
B. Boiling pt elevation 2. Number of solute particles
C. Freezing pt depression 3. i × Kf × m
D. Vapour pressure lowering 4. Raoult’s law
Column I Column II
A. Pickling vegetables 1. Osmosis
B. IV drips 2. Isotonic solution
C. Desalination 3. Reverse osmosis
D. Road salt 4. Freezing point depression
Column I Column II
A. VP lowering 1. Non-volatile solute added
B. BP elevation 2. More heat needed
C. FP depression 3. Solution stays liquid longer
D. Osmosis 4. Solvent flows through membrane
Column I Column II
A. ΔTf = iKfm 1. Freezing pt depression
Column I Column II
B. ΔTb = iKbm 2. Boiling pt elevation
C. π = iCRT 3. Osmotic pressure
D. ΔP / P₀ = χsolute 4. Vapour pressure lowering
Column I Column II
A. Isotonic 1. Same osmotic pressure
B. Hypertonic 2. Higher solute conc.
C. Hypotonic 3. Lower solute conc.
D. Azeotrope 4. Constant boiling
Column I Column II
A. Sugar in water 1. Non-electrolyte
B. NaCl in water 2. Electrolyte
C. Ethanol in water 3. Liquid-liquid
D. Air 4. Gas-gas solution
Column I Column II
A. Gas solubility 1. Henry’s law
B. VP of components 2. Raoult’s law
C. Total pressure (gas) 3. Dalton’s law
D. Osmotic pressure 4. Van’t Hoff equation
Column I Column II
A. Temp ↑ 1. Osmotic pressure ↑
B. Pressure ↑ 2. Gas solubility ↑
C. i ↑ 3. Greater colligative effect
D. m ↑ 4. Stronger effect
Column I Column II
A. Mole fraction 1. moles of A / total moles
B. Molality 2. moles of solute / kg of solvent
C. Molarity 3. moles of solute / L of solution
D. Parts per million 4. (mass of solute / total mass) × 10⁶
Column I Column II
A. ΔTb = iKbm 1. Kb = molal elevation constant
B. ΔTf = iKfm 2. Kf = molal depression constant
C. π = iCRT 3. R = universal gas constant
D. i (Van’t Hoff) 4. accounts for particle dissociation
Column I Column II
A. O₂ dissolved in water 1. Gas in liquid
B. Ethanol in water 2. Liquid in liquid
C. Sugar in tea 3. Solid in liquid
D. Air (O₂ + N₂) 4. Gas in gas
Column I Column II
A. NaCl in water 1. i = 2, increases colligative effect
B. Glucose in water 2. i = 1, no dissociation
C. BaCl₂ in water 3. i = 3
Column I Column II
D. CH₃COOH in water 4. i between 1 and 2 (partial)
Column I Column II
A. Positive deviation 1. Weaker A–B interactions
B. Negative deviation 2. Stronger A–B interactions
C. Ideal solution 3. A–B ≈ A–A and B–B
D. Azeotrope 4. Constant boiling mixture
Column I Column II
A. Vapour pressure 1. mmHg or atm
B. Osmotic pressure 2. atm
C. Partial pressure 3. atm
D. Freezing point 4. Kelvin (K)
Column I Column II
A. Raoult’s law 1. VP ∝ mole fraction
B. Henry’s law 2. C ∝ p (gas solubility)
C. Van’t Hoff 3. π = iCRT
D. Dalton’s law 4. Total P = p₁ + p₂ + …
Column I Column II
A. Soda water 1. Gas in liquid
B. Vinegar 2. Liquid in liquid
C. Seawater 3. Solid in liquid
D. Air 4. Gas in gas
Answer: A-1, B-2, C-3, D-4
Column I Column II
A. Osmotic pressure 1. Pressure to stop osmosis
B. Semipermeable membrane 2. Allows solvent but not solute
C. Reverse osmosis 3. Pressure > π to reverse solvent flow
D. Colligative property 4. Depends on number of solute particles
Column I Column II
A. IV fluids (saline) 1. Isotonic solutions
B. Desalination of seawater 2. Reverse osmosis
C. Antifreeze in car engines 3. Freezing point depression
D. Food preservation (salt/sugar) 4. Osmotic pressure