CUET UG Chemistry Booster Test - 3 Freezing, Osmosis, and van\'t Hoff Factor
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QUESTION 1 OF 20
Statements regarding the freezing point of substances:
1. At the freezing point, the solid phase is in dynamic equilibrium with the liquid phase.
2. Vapour pressure of the liquid phase is higher than the solid phase at the freezing point.
3. Addition of a non-volatile solute decreases the solvent's vapour pressure.
4. A solution freezes when its vapour pressure is greater than the pure solid solvent.
QUESTION 2 OF 20
Arrange the following states in decreasing order of temperature at 1 atm pressure:
1. Boiling point of aqueous sucrose solution
2. Boiling point of pure water
3. Freezing point of pure water
4. Freezing point of aqueous sucrose solution
QUESTION 3 OF 20
Match List-I (Solvent) with List-II (Kf value in K kg mol⁻¹):
| List 1 (Solvent) | List 2 (Kf Value) |
|---|---|
| 1. Water | a. 1.86 |
| 2. Benzene | b. 5.12 |
| 3. Cyclohexane | c. 20.00 |
| 4. Carbon tetrachloride | d. 31.8 |
QUESTION 4 OF 20
What formal term is used for the constant 'Kf' when calculating the molar mass of a solute from freezing point data?
QUESTION 5 OF 20
QUESTION 6 OF 20
QUESTION 7 OF 20
The excess pressure that just stops the flow of solvent across a semipermeable membrane is defined as:
QUESTION 8 OF 20
In the osmotic pressure equation P = CRT, if C is expressed in mol L⁻¹ and T in Kelvin, what is the unit of the gas constant R typically used when P is measured in bar?
QUESTION 9 OF 20
When blood cells are placed in a 0.9% (mass/volume) sodium chloride solution, what type of net osmotic process occurs?
QUESTION 10 OF 20
If blood cells are placed in a solution containing more than 0.9% (mass/volume) sodium chloride, what will happen?
QUESTION 11 OF 20
Statements regarding reverse osmosis in desalination:
1. Pure water is squeezed out of the sea water through the membrane.
2. Pressure less than osmotic pressure must be applied.
3. The direction of osmosis is reversed.
4. The pressure required is quite low.
QUESTION 12 OF 20
Match List-I with List-II concerning membrane types and processes:
| List 1 (Membrane / Process) | List 2 (Description) |
|---|---|
| 1. Cellulose acetate | a. Synthetic membrane for RO |
| 2. Pig's bladder | b. Natural semipermeable membrane |
| 3. Reverse Osmosis | c. Pressure larger than osmotic pressure applied |
| 4. Desalination | d. Used to meet potable water requirements |
QUESTION 13 OF 20
When 1 mole of KCl dissolves in water, assuming complete dissociation, the experimentally determined molar mass is lower than the true value. What is this resultant calculated molar mass called?
QUESTION 14 OF 20
Arrange the following terms based on the extent of particles present in 1 mole of substance after dissolution (from highest to lowest):
1. Complete dissociation of K₂SO₄
2. Complete dissociation of NaCl
3. Glucose in water
4. Complete dimerisation of ethanoic acid in benzene
QUESTION 15 OF 20
What is the symbol used to denote the ratio of normal molar mass to abnormal molar mass?
QUESTION 16 OF 20
Identify the mathematical relationship representing the van't Hoff factor (i):
QUESTION 17 OF 20
Statements regarding modified colligative equations:
1. Elevation of boiling point is ΔTb = i Kb m
2. Osmotic pressure is P = i n₂ R T / V
3. Relative lowering of vapour pressure incorporates 'i'
4. 'i' is only used for non-electrolytes
QUESTION 18 OF 20
For ethanoic acid in benzene undergoing complete association (dimerisation), the value of the van't Hoff factor 'i' incorporated in equations is nearly:
QUESTION 19 OF 20
Match List-I (Electrolyte) with List-II (Limiting van't Hoff factor 'i' at complete dissociation):
| List 1 (Electrolyte / Solute) | List 2 (Limiting van't Hoff Factor) |
|---|---|
| 1. K₂SO₄ | a. i approaches 3 |
| 2. NaCl | b. i approaches 2 |
| 3. Ethanoic acid in benzene | c. i approaches 0.5 |
| 4. Glucose | d. i is 1 |
QUESTION 20 OF 20
In very dilute solutions (e.g., 0.001 m), the experimental van't Hoff factor (i) for MgSO₄ approaches:
Test Complete!
Answer Review
1 Statements regarding the freezing point of substances:
1. At the freezing point, the solid phase is in dynamic equilibrium with the liquid phase.
2. Vapour pressure of the liquid phase is higher than the solid phase at the freezing point.
3. Addition of a non-volatile solute decreases the solvent's vapour pressure.
4. A solution freezes when its vapour pressure is greater than the pure solid solvent.
�� Freezing point involves solid-liquid equilibrium. �� At freezing point, vapour pressures are equal. 1. • Non-volatile solute lowers solvent vapour pressure.
2. → At the freezing point, solid and liquid phases coexist in dynamic equilibrium. Also, addition of a non-volatile solute lowers the vapour pressure of the solvent. Statement 2 is incorrect because vapour pressures are equal at freezing point. Statement 4 is incorrect because freezing occurs when solution vapour pressure equals that of the pure solid solvent.
- �� Option A → Includes Statement 2, which is incorrect.
- �� Option C → Includes Statement 4, which is incorrect.
- 3. • Option D → Includes Statement 2, which is incorrect.
Used
- 4. Elimination
Application:
- �� Remove options containing incorrect vapour pressure statements.
Final Logic:
- �� Only Statements 1 and 3 are correct.
1. → Freezing = Equal Vapour Pressure.
2 Arrange the following states in decreasing order of temperature at 1 atm pressure:
1. Boiling point of aqueous sucrose solution
2. Boiling point of pure water
3. Freezing point of pure water
4. Freezing point of aqueous sucrose solution
�� Solute elevates boiling point. �� Solute depresses freezing point. 1. • Therefore, solution BP > pure water BP > pure water FP > solution FP.
2. → Adding a non-volatile solute like sucrose increases the boiling point and decreases the freezing point of water. Therefore, in decreasing order of temperature: Boiling point of sucrose solution > Boiling point of pure water > Freezing point of pure water > Freezing point of sucrose solution.
- �� Option B → Places pure water boiling point above solution boiling point.
- �� Option C → Places solution freezing point above pure water freezing point.
- 1. • Option D → Gives reverse-type ordering.
Used
- 2. Option Grouping
Application:
- �� Apply boiling point elevation and freezing point depression.
Final Logic:
- �� Non-volatile solute raises BP and lowers FP.
1. → Solute: Boiling Up, Freezing Down.
3 Match List-I (Solvent) with List-II (Kf value in K kg mol⁻¹):
| List 1 (Solvent) | List 2 (Kf Value) |
|---|---|
| 1. Water | a. 1.86 |
| 2. Benzene | b. 5.12 |
| 3. Cyclohexane | c. 20.00 |
| 4. Carbon tetrachloride | d. 31.8 |
�� Water has Kf = 1.86. �� Benzene has Kf = 5.12. �� Cyclohexane has Kf = 20.00. 1. • Carbon tetrachloride has Kf = 31.8.
2. → The molal depression constant is solvent-specific. The correct NCERT values are: Water = 1.86 K kg mol⁻¹ Benzene = 5.12 K kg mol⁻¹ Cyclohexane = 20.00 K kg mol⁻¹ Carbon tetrachloride = 31.8 K kg mol⁻¹
- �� Option B → Water and carbon tetrachloride values are incorrectly matched.
- �� Option C → Water and benzene values are interchanged.
- 1. • Option D → Multiple Kf values are incorrectly matched.
Used
- 2. Option Grouping
Application:
- �� Match standard Kf values with their solvents.
Final Logic:
- �� Water-1.86, Benzene-5.12, Cyclohexane-20.00, Carbon tetrachloride-31.8.
1. → Water lowest, CCl₄ highest.
4 What formal term is used for the constant 'Kf' when calculating the molar mass of a solute from freezing point data?
�� Kf is used in freezing point depression. �� It is called molal depression constant. 1. • It is also called cryoscopic constant.
2. → The constant Kf used in freezing point depression calculations is known as the molal depression constant or cryoscopic constant. Readable Formula: Depression in Freezing Point = Kf × Molality
- �� Option A → Ebullioscopic constant refers to boiling point elevation constant Kb.
- �� Option C → Osmotic constant is not the term used for Kf.
- 1. • Option D → Henry's constant is used in gas solubility.
Used
- 2. Odd One Out
Application:
- �� Connect "cryo" with freezing.
Final Logic:
- �� Freezing point depression constant = cryoscopic constant.
1. → Cryo means freezing.
5
�� SPM allows selective passage. �� Small solvent molecules pass through. 1. • Larger solute particles are blocked.
2. → According to the passage, semipermeable membranes contain submicroscopic pores that allow small solvent molecules like water to pass through. Larger solute molecules cannot pass freely.
- �� Option A → Macromolecules are too large to pass through.
- �� Option B → Solute molecules are hindered.
- 3. • Option D → Both solute and solvent cannot freely pass through SPM.
Used
- 4. Contextual/Tonal Matching
Application:
- �� Use the direct statement from the passage.
Final Logic:
- �� SPM permits small solvent molecules only.
1. → SPM = Solvent Passes Membrane.
6
�� Osmosis is solvent movement. �� Solvent moves from dilute side to concentrated side. 1. • Pure solvent moves toward solution.
2. → During osmosis, solvent molecules pass through a semipermeable membrane from pure solvent or dilute solution toward the more concentrated solution. This continues until equilibrium is reached.
- �� Option A → Natural osmosis occurs from pure solvent to solution, not generally solution to pure solvent.
- �� Option B → This reverses the correct direction.
- 3. • Option D → Net flow is not equal in both directions before equilibrium.
Used
- 4. Contextual/Tonal Matching
Application:
- �� Use the passage definition of solvent flow.
Final Logic:
- �� Osmosis = solvent flow from lower concentration to higher concentration.
1. → Solvent moves to stronger solution.
7 The excess pressure that just stops the flow of solvent across a semipermeable membrane is defined as:
�� Osmotic pressure stops osmosis. �� It is applied on the solution side. 1. • It prevents net solvent flow.
2. → Osmotic pressure is the minimum excess pressure that must be applied to a solution to stop the flow of solvent through a semipermeable membrane.
- �� Option A → Atmospheric pressure is external air pressure.
- �� Option B → Vapour pressure is pressure exerted by vapour.
- 3. • Option D → Hydrostatic pressure is pressure due to liquid column, not the defined colligative pressure.
Used
- 4. Contextual/Tonal Matching
Application:
- �� Match the phrase "just stops solvent flow" with osmotic pressure.
Final Logic:
- �� Pressure required to stop osmosis = osmotic pressure.
1. → Osmotic Pressure Stops Osmosis.
8 In the osmotic pressure equation P = CRT, if C is expressed in mol L⁻¹ and T in Kelvin, what is the unit of the gas constant R typically used when P is measured in bar?
�� Osmotic pressure is measured in bar. �� Concentration is mol per litre. 1. • R must match litre and bar units.
2. → In the equation: Readable Formula: Osmotic Pressure = Molarity × Gas Constant × Temperature If osmotic pressure is in bar, concentration is in mol L⁻¹ and temperature is in Kelvin, then R should have the unit: L bar mol⁻¹ K⁻¹ This ensures the final pressure unit becomes bar.
- �� Option A → Used when energy is expressed in joules.
- �� Option B → Used when pressure is measured in atm.
- 1. • Option D → Used when pressure is in pascal and volume in cubic metre.
Used
- 2. Dimensional/Unit Analysis
Application:
- �� Match the units of pressure, concentration and temperature in the equation.
Final Logic:
- �� For pressure in bar, R must contain L bar mol⁻¹ K⁻¹.
1. → Bar pressure needs R in L bar.
9 When blood cells are placed in a 0.9% (mass/volume) sodium chloride solution, what type of net osmotic process occurs?
�� 0.9% NaCl is normal saline. �� It is isotonic with blood cells. 1. • No net water movement occurs.
2. → A 0.9% mass/volume NaCl solution is isotonic with the fluid inside blood cells. Since the osmotic pressure inside and outside the cells is balanced, there is no net movement of water across the cell membrane.
- �� Option A → Plasmolysis occurs in hypertonic solution when cells lose water.
- �� Option B → Hemolysis occurs in hypotonic solution when cells swell and burst.
- 3. • Option C → Reverse osmosis requires applied pressure greater than osmotic pressure.
Used
- 4. Contextual/Tonal Matching
Application:
- �� Connect 0.9% NaCl with isotonic solution.
Final Logic:
- �� Isotonic solution causes no net osmosis.
1. → 0.9% = No Net Flow.
10 If blood cells are placed in a solution containing more than 0.9% (mass/volume) sodium chloride, what will happen?
�� More than 0.9% NaCl is hypertonic. �� Water leaves the cells. 1. • Cells shrink.
2. → A solution containing more than 0.9% NaCl is hypertonic compared to blood cells. Water moves out of the cells toward the more concentrated external solution by osmosis. As a result, the cells shrink.
- �� Option A → This happens in hypotonic solution.
- �� Option C → No net flow occurs only in isotonic solution.
- 3. • Option D → Reverse osmosis requires external pressure, not normal cell osmosis.
Used
- 4. Elimination
Application:
- �� Identify hypertonic solution and remove options describing hypotonic or isotonic conditions.
Final Logic:
- �� Hypertonic solution pulls water out of cells.
1. → Hypertonic = Water exits.
11 Statements regarding reverse osmosis in desalination:
1. Pure water is squeezed out of the sea water through the membrane.
2. Pressure less than osmotic pressure must be applied.
3. The direction of osmosis is reversed.
4. The pressure required is quite low.
�� Reverse osmosis reverses natural osmosis. �� Pressure greater than osmotic pressure is applied. 1. • Pure water passes through the membrane.
2. → In reverse osmosis, pressure greater than the osmotic pressure is applied to the solution side. This forces pure water through the semipermeable membrane, reversing the natural direction of osmosis. Hence Statements 1 and 3 are correct. Statements 2 and 4 are incorrect because high pressure, not low pressure, is required.
- �� Option B → Statements 2 and 4 are incorrect.
- �� Option C → Statement 4 is incorrect.
- 3. • Option D → Statement 2 is incorrect.
Used
- 4. Elimination
Application:
- �� Remove statements contradicting the definition of reverse osmosis.
Final Logic:
- �� Reverse osmosis requires pressure greater than osmotic pressure and reverses solvent flow.
1. → RO = Reverse + High Pressure.
12 Match List-I with List-II concerning membrane types and processes:
| List 1 (Membrane / Process) | List 2 (Description) |
|---|---|
| 1. Cellulose acetate | a. Synthetic membrane for RO |
| 2. Pig's bladder | b. Natural semipermeable membrane |
| 3. Reverse Osmosis | c. Pressure larger than osmotic pressure applied |
| 4. Desalination | d. Used to meet potable water requirements |
�� Cellulose acetate is a synthetic RO membrane. �� Pig's bladder is a natural semipermeable membrane. �� Reverse osmosis requires pressure greater than osmotic pressure. 1. • Desalination provides potable water.
2. → The correct matching is: Cellulose acetate → Synthetic membrane for RO Pig's bladder → Natural semipermeable membrane Reverse Osmosis → Pressure larger than osmotic pressure applied Desalination → Used to meet potable water requirements This is the standard NCERT description of reverse osmosis and membrane applications.
- �� Option B → Multiple membrane-process mismatches.
- �� Option C → Pig's bladder and reverse osmosis incorrectly matched.
- 1. • Option D → Cellulose acetate and desalination incorrectly matched.
Used
- 2. Option Grouping
Application:
- �� Match each membrane/process with its defining characteristic.
Final Logic:
- �� Cellulose acetate–RO membrane, Pig's bladder–natural membrane, RO–high pressure, Desalination–drinking water.
1. → Cellulose–RO, Pig–Natural.
13 When 1 mole of KCl dissolves in water, assuming complete dissociation, the experimentally determined molar mass is lower than the true value. What is this resultant calculated molar mass called?
�� KCl dissociates into ions. �� Colligative properties become larger than expected. 1. • Calculated molar mass becomes lower than true molar mass.
2. → KCl dissociates into K⁺ and Cl⁻ ions, increasing the number of particles in solution. Since colligative properties depend on particle number, the experimentally calculated molar mass becomes smaller than the actual molar mass. Such a value is called an abnormal molar mass.
- �� Option A → Normal molar mass is the actual molar mass.
- �� Option C → Theoretical molar mass is not the NCERT term.
- 3. • Option D → Associated molar mass is related to association, not dissociation.
Used
- 4. Contextual/Tonal Matching
Application:
- �� Relate dissociation with abnormal colligative behavior.
Final Logic:
- �� Dissociation causes abnormal molar mass values.
1. → More particles → Lower calculated molar mass.
14 Arrange the following terms based on the extent of particles present in 1 mole of substance after dissolution (from highest to lowest):
1. Complete dissociation of K₂SO₄
2. Complete dissociation of NaCl
3. Glucose in water
4. Complete dimerisation of ethanoic acid in benzene
�� K₂SO₄ gives 3 particles. �� NaCl gives 2 particles. �� Glucose gives 1 particle. 1. • Dimerisation reduces particles to 0.5 mole equivalents.
2. → Number of particles produced: K₂SO₄ → 2K⁺ + SO₄²⁻ = 3 particles NaCl → Na⁺ + Cl⁻ = 2 particles Glucose → no dissociation = 1 particle Ethanoic acid dimerisation → particle number decreases to about half Therefore: K₂SO₄ > NaCl > Glucose > Ethanoic acid (dimerised)
- �� Option B → Completely reverses the correct trend.
- �� Option C → Places NaCl above K₂SO₄ incorrectly.
- 1. • Option D → Places glucose above NaCl incorrectly.
Used
- 2. Option Grouping
Application:
- �� Count particles after dissociation or association.
Final Logic:
- �� More particles correspond to higher position in the order.
1. → 3 > 2 > 1 > 0.5
15 What is the symbol used to denote the ratio of normal molar mass to abnormal molar mass?
�� i denotes van't Hoff factor. �� It explains abnormal colligative behavior. 1. • It relates normal and abnormal molar masses.
2. → The van't Hoff factor (i) is used to account for association and dissociation of solutes. Readable Expression: i = Normal Molar Mass / Abnormal Molar Mass It also equals: i = Observed Colligative Property / Calculated Colligative Property
- �� Option A → Kf is cryoscopic constant.
- �� Option C → P commonly denotes pressure.
- 1. • Option D → R is the gas constant.
Used
- 2. Direct Recall
Application:
- �� Identify the symbol associated with abnormal molar mass.
Final Logic:
- �� van't Hoff factor is represented by i.
1. → i = irregularity factor.
16 Identify the mathematical relationship representing the van't Hoff factor (i):
�� van't Hoff factor corrects abnormal colligative values. �� It compares observed and calculated colligative properties. 1. • It accounts for association or dissociation.
2. → The van't Hoff factor is represented as: Readable Expression: van't Hoff factor = Observed Colligative Property ÷ Calculated Colligative Property It can also be written as: van't Hoff factor = Normal Molar Mass ÷ Abnormal Molar Mass Therefore, Option C is correct.
- �� Option A → This is the inverse of the correct molar mass relationship.
- �� Option B → This is the inverse of the correct colligative property relationship.
- 1. • Option D → This is not the standard NCERT definition.
Used
- 2. Elimination
Application:
- �� Compare each option with the standard definition of van't Hoff factor.
Final Logic:
- �� i = Observed value ÷ Calculated value.
1. → i = Observed over Calculated.
17 Statements regarding modified colligative equations:
1. Elevation of boiling point is ΔTb = i Kb m
2. Osmotic pressure is P = i n₂ R T / V
3. Relative lowering of vapour pressure incorporates 'i'
4. 'i' is only used for non-electrolytes
�� Modified equations include van't Hoff factor. �� i corrects values for association or dissociation. 1. • i is not only for non-electrolytes.
2. → Modified colligative equations include the van't Hoff factor to correct for association or dissociation. Readable Formulae: Elevation in Boiling Point = i × Kb × Molality Osmotic Pressure = i × Number of Moles of Solute × Gas Constant × Temperature ÷ Volume Relative Lowering of Vapour Pressure also incorporates i when abnormal association or dissociation affects particle count. Statement 4 is incorrect because i is mainly used when solutes associate or dissociate, especially electrolytes.
- �� Option B → Omits Statement 3, which is correct.
- �� Option C → Includes Statement 4, which is incorrect.
- 1. • Option D → Includes Statement 4, which is incorrect.
Used
- 2. Elimination
Application:
- �� Remove options containing the false statement that i is only used for non-electrolytes.
Final Logic:
- �� Statements 1, 2 and 3 correctly use van't Hoff factor.
1. → Add i when particles change.
18 For ethanoic acid in benzene undergoing complete association (dimerisation), the value of the van't Hoff factor 'i' incorporated in equations is nearly:
�� Two ethanoic acid molecules associate into one dimer. �� Particle number becomes half. 1. • Therefore, i becomes nearly 0.5.
2. → In benzene, ethanoic acid molecules associate due to hydrogen bonding. Readable Expression: 2 Ethanoic Acid Molecules combine to form 1 Dimer So, the number of solute particles becomes half of the expected number. Therefore, the van't Hoff factor becomes nearly 0.5.
- �� Option B → Represents no association or dissociation.
- �� Option C → Represents dissociation into two particles.
- 1. • Option D → Represents dissociation into three particles.
Used
- 2. Substitution
Application:
- �� Convert two associated molecules into one particle and compare particle count.
Final Logic:
- �� Complete dimerisation halves particle number, so i = 0.5.
1. → Dimer means two become one.
19 Match List-I (Electrolyte) with List-II (Limiting van't Hoff factor 'i' at complete dissociation):
| List 1 (Electrolyte / Solute) | List 2 (Limiting van't Hoff Factor) |
|---|---|
| 1. K₂SO₄ | a. i approaches 3 |
| 2. NaCl | b. i approaches 2 |
| 3. Ethanoic acid in benzene | c. i approaches 0.5 |
| 4. Glucose | d. i is 1 |
�� K₂SO₄ gives 3 ions. �� NaCl gives 2 ions. �� Ethanoic acid associates, so i is nearly 0.5. 1. • Glucose does not dissociate, so i = 1.
2. → The correct matching is: K₂SO₄ → 2K⁺ + SO₄²⁻ → i approaches 3 NaCl → Na⁺ + Cl⁻ → i approaches 2 Ethanoic acid in benzene → dimerisation → i approaches 0.5 Glucose → no association or dissociation → i is 1
- �� Option B → NaCl, ethanoic acid and glucose are incorrectly matched.
- �� Option C → K₂SO₄ and glucose are incorrectly matched.
- 1. • Option D → Multiple solute-i relationships are incorrect.
Used
- 2. Option Grouping
Application:
- �� Match each solute based on particle number after dissociation or association.
Final Logic:
- �� i depends on the number of particles formed.
1. → K₂SO₄ = 3, NaCl = 2, Acid dimer = 0.5, Glucose = 1.
20 In very dilute solutions (e.g., 0.001 m), the experimental van't Hoff factor (i) for MgSO₄ approaches:
�� MgSO₄ dissociates into two ions. �� Very dilute solution supports near-complete dissociation. 1. • Therefore, i approaches 2.
2. → Magnesium sulfate dissociates as: Readable Expression: MgSO₄ dissociates into Mg²⁺ and SO₄²⁻ Total particles formed = 2 In very dilute solutions, dissociation becomes nearly complete. Hence, the van't Hoff factor approaches 2.00.
- �� Option A → Too low for near-complete dissociation.
- �� Option B → Possible for partial dissociation, not the limiting dilute value.
- 1. • Option D → Would require formation of three particles.
Used
- 2. Substitution
Application:
- �� Count ions produced by complete dissociation of MgSO₄.
Final Logic:
- �� MgSO₄ produces two ions, so i approaches 2.
1. → MgSO₄ = 2 ions.
