A solution is labelled 12% (w/w) glucose. Which interpretation is correct?
(a)12 g glucose is present in 100 mL solution.
(b)12 g glucose is present in 100 g solution.
(c)12 mL glucose is present in 100 mL solution.
(d)12 g glucose is present in 100 g solvent.
Show answer
(b) 12 g glucose is present in 100 g solution.
Mass percentage uses mass of component divided by total mass of solution, multiplied by 100.
Question 2
What does 5% (w/v) NaCl mean?
(a)5 g NaCl is present in 100 mL solution.
(b)5 g NaCl is present in 100 g solution.
(c)5 g NaCl is mixed with exactly 100 mL water.
(d)5 mL NaCl is present in 100 mL solution.
Show answer
(a) 5 g NaCl is present in 100 mL solution.
Mass-by-volume percentage specifies grams of solute per 100 mL of final solution.
Solubility and Henry's law for gases
Question 3
Powdered NH4Cl dissolves faster than equal-mass crystals at the same temperature. What follows about equilibrium solubility?
(a)The powder has greater equilibrium solubility because it dissolves faster.
(b)The crystals have greater equilibrium solubility because they are larger.
(c)Both forms have the same equilibrium solubility.
(d)Neither form has a defined equilibrium solubility.
Show answer
(c) Both forms have the same equilibrium solubility.
Particle size changes dissolution rate through surface area, not the equilibrium solubility at fixed temperature.
Question 4
A soluble solid is added to water at fixed temperature and pressure. While some solid is still present, stirring increases mixing near its surface and makes it dissolve faster. Which property remains unchanged?
(a)The motion of undissolved particles in the liquid.
(b)The mixing rate near the solid surface.
(c)The instantaneous dissolution rate.
(d)The equilibrium solubility at that temperature.
Show answer
(d) The equilibrium solubility at that temperature.
Dissolution rate describes how quickly solid enters the solution. Stirring improves contact and transport near the solid surface, so the rate can increase.
Equilibrium solubility describes the maximum amount that can remain dissolved in a specified amount of solvent at the stated temperature and pressure. Stirring alone does not change that limit.
The unchanged property is equilibrium solubility. Faster dissolution does not mean a greater equilibrium solubility.
Raoult's law and vapour pressure of liquid solutions
Question 5
A non-volatile solute is added to a volatile solvent at fixed temperature. Which statement is correct?
(a)The vapour must have the same solute-solvent composition as the liquid.
(b)The solute adds its own vapour and raises total pressure.
(c)The pure-solvent vapour pressure increases.
(d)The solvent vapour pressure falls, and the vapour contains only solvent.
Show answer
(d) The solvent vapour pressure falls, and the vapour contains only solvent.
A non-volatile solute contributes no vapour and lowers the solvent mole fraction; the equilibrium vapour is therefore solvent while its pressure is reduced.
Question 6
A volatile binary liquid has unequal pure-component vapour pressures. At equilibrium, what distinguishes vapour from liquid?
(a)The vapour and liquid must have identical compositions.
(b)The vapour is enriched in the more volatile component.
(c)Adding a non-volatile component would raise the vapour pressure.
(d)Only the less volatile component can enter the vapour.
Show answer
(b) The vapour is enriched in the more volatile component.
Unequal escaping tendencies make the vapour richer in the component with the greater pure vapour pressure.
Ideal solutions, non-ideal deviations, and azeotropes
Question 7
A solution shows a large positive deviation from Raoult's law. Which statement is correct?
(a)Weaker unlike attractions produce a maximum-boiling azeotrope.
(b)It forms a minimum-boiling azeotrope that ordinary fractional distillation fully separates.
(c)Positive deviation lowers vapour pressure below both pure liquids.
(d)It can form a minimum-boiling azeotrope that ordinary fractional distillation cannot cross.
Show answer
(d) It can form a minimum-boiling azeotrope that ordinary fractional distillation cannot cross.
Positive deviation raises vapour pressure and can create a boiling minimum; at the azeotrope liquid and vapour compositions coincide.
Question 8
Why can an azeotrope not be separated into pure components by ordinary fractional distillation?
(a)Its components always have identical pure boiling points.
(b)Its interaction deviation must be opposite to that implied by its boiling extremum.
(c)Repeated fractional distillation always separates it completely despite equal vapour and liquid compositions.
(d)Its liquid and equilibrium vapour have the same composition.
Show answer
(d) Its liquid and equilibrium vapour have the same composition.
Distillation enriches a vapour only when vapour and liquid compositions differ; at an azeotrope they coincide.
Colligative properties and relative lowering of vapour pressure
Question 9
Which method correctly compares ideal colligative effects in the same solvent?
(a)Ignore both particle count and solvent amount.
(b)Compare effective particle molality, i m.
(c)Swap solute and solvent masses before calculating molality.
(d)Rank the solutions by the chemical identity or molar mass of the solute.
Show answer
(b) Compare effective particle molality, i m.
A colligative effect is governed by dissolved-particle concentration; solvent mass remains the molality denominator.
Question 10
Two solutions in the same solvent have equal effective particle molality. Which conclusion is valid?
(a)They have equal ideal magnitudes of the same colligative property.
(b)The chemically heavier solute must give the larger effect.
(c)The effect changes if solute mass is used where solvent mass belongs.
(d)The electrolyte must always give the larger effect, even after i is included.
Show answer
(a) They have equal ideal magnitudes of the same colligative property.
Once effective particle concentration is equal in the same solvent, identity does not change the ideal colligative magnitude.
Depression of freezing point and molar-mass calculation
Question 11
Which statement about the molal freezing-point depression constant Kf is correct?
(a)Kf multiplies molarity measured per litre of solution.
(b)Kf is an absolute temperature to which 273.15 must be added.
(c)Kf is fixed by the chemical identity of the solute.
(d)Kf is a property of the solvent and multiplies molality.
Show answer
(d) Kf is a property of the solvent and multiplies molality.
Kf sets the depression per unit molality for a given solvent; concentration changes ΔTf, not Kf.
Question 12
Which setup correctly uses ΔTf=Kfm?
(a)Use grams of solvent per mole of solute.
(b)Use moles of solute per litre of solution.
(c)Add 273.15 to the calculated temperature difference.
(d)Use moles of solute per kilogram of solvent, with no 273.15 correction to ΔTf.
Show answer
(d) Use moles of solute per kilogram of solvent, with no 273.15 correction to ΔTf.
The symbol m denotes molality, and kelvin and Celsius temperature intervals have the same numerical magnitude.
Elevation of boiling point and molar-mass calculation
Question 13
One mole NaCl is dissolved in 1.000 kg water and dissociates completely. With water's Kb=0.52 K kg mol^-1, what boiling point is predicted?
(a)103.72 °C after incorrectly choosing a constant for the solute instead of water's Kb.
(b)98.96 °C
(c)101.04 °C
(d)About 101.02 °C after incorrectly using solution mass as the molality denominator.
Show answer
(c) 101.04 °C
Complete NaCl dissociation gives i=2, so ΔTb=2×0.52×1.0=1.04 K and Tb=101.04 °C.
Osmosis, osmotic pressure, tonicity, and reverse osmosis
Question 14
A red blood cell is placed in an isotonic solution. Which statement is correct?
(a)Water enters and the cell swells because isotonic means hypotonic.
(b)Equal density, rather than osmotic pressure, prevents flow.
(c)There is no net water flow, so the cell retains its normal volume.
(d)Water flows out to the solution because solvent always moves toward dilution.
Show answer
(c) There is no net water flow, so the cell retains its normal volume.
Isotonic solutions have equal osmotic pressure at the stated temperature, so opposing solvent flows balance.
Abnormal molar masses and the van't Hoff factor
Question 15
A solute undergoes complete tetramerisation. What is its ideal van't Hoff factor?
(a)0.25 (dimensionless)
(b)4.00 (dimensionless)
(c)0.50 (dimensionless)
(d)1.00 (dimensionless)
Show answer
(a) 0.25 (dimensionless)
Four monomers become one particle, so particles after/before=1/4=0.25.
Warming expands the example solution. The volume-based concentration falls while the mass-based concentration stays fixed.
A closed sample has 1.00 mol of solute in 1.00 L of solution made with 1.00 kg of solvent.
If volume grows to 1.02 L, molarity falls to 0.98 mol/L while molality stays 1.00 mol/kg.
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