Online Test — Solutions
20 Questions • 15 min • Chapter MCQ
15:00
Question 1 of 20
Molarity is defined as moles of solute per:
kg of solvent
litre of solution
litre of solvent
kg of solution
Explanation: Molarity $M=n/V$ uses litres of solution.
Question 2 of 20
Which concentration term is temperature-dependent?
Mole fraction
Molality
Molarity
Mass percentage
Explanation: Volume changes with temperature, so molarity varies.
Question 3 of 20
Henry's law is expressed as:
$p=K_H/x$
$p=K_H x$
$x=K_H p^2$
$p=x/K_H$
Explanation: Partial pressure is proportional to mole fraction: $p=K_H x$.
Question 4 of 20
Solubility of a gas in a liquid generally:
increases with temperature
decreases with pressure
decreases with temperature
is independent of pressure
Explanation: Gas dissolution is exothermic, so higher temperature lowers solubility.
Question 5 of 20
For an ideal solution, $\Delta_{mix}H$ and $\Delta_{mix}V$ are:
both positive
both negative
both zero
positive and negative respectively
Explanation: Ideal solutions show no enthalpy or volume change on mixing.
Question 6 of 20
Ethanol + water is an example of:
ideal solution
positive deviation
negative deviation
maximum-boiling azeotrope only
Explanation: Weaker A–B interactions give higher-than-ideal vapour pressure (positive deviation).
Question 7 of 20
Acetone + chloroform shows negative deviation because:
A–B forces are weaker
hydrogen bonding strengthens A–B forces
there is no interaction
both are non-polar
Explanation: Hydrogen bonding between unlike molecules lowers vapour pressure.
Question 8 of 20
A minimum-boiling azeotrope is associated with:
large negative deviation
ideal behaviour
large positive deviation
zero deviation
Explanation: Positive deviation produces a vapour-pressure maximum, hence a boiling-point minimum.
Question 9 of 20
The relative lowering of vapour pressure equals the:
mole fraction of solvent
mole fraction of solute
molality
molarity
Explanation: $(p^0-p)/p^0=x_{solute}$.
Question 10 of 20
Which of the following is NOT a colligative property?
Osmotic pressure
Boiling point of pure water
Depression of freezing point
Relative lowering of vapour pressure
Explanation: Colligative properties relate to the solution, not the pure solvent's boiling point.
Question 11 of 20
The elevation of boiling point is given by:
$\Delta T_b=K_f m$
$\Delta T_b=K_b m$
$\Delta T_b=CRT$
$\Delta T_b=p^0 x$
Explanation: $\Delta T_b=K_b m$ where $K_b$ is the ebullioscopic constant.
Question 12 of 20
Ethylene glycol is added to car radiators to:
raise vapour pressure
depress the freezing point
increase density only
speed up boiling
Explanation: It depresses the freezing point, preventing the coolant from freezing.
Question 13 of 20
Osmotic pressure $\Pi$ for a dilute solution equals:
$K_b m$
$CRT$
$K_f m$
$x p^0$
Explanation: $\Pi=CRT$ with $C$ the molar concentration.
Question 14 of 20
Two solutions with the same osmotic pressure are called:
hypertonic
hypotonic
isotonic
saturated
Explanation: Equal osmotic pressure means the solutions are isotonic.
Question 15 of 20
For NaCl dissolving completely in water, the van't Hoff factor is about:
0.5
1
2
3
Explanation: NaCl gives 2 ions, so $i\approx2$.
Question 16 of 20
A van't Hoff factor less than 1 indicates:
dissociation
no change
association
ionisation
Explanation: Association reduces particle count, giving $i<1$ (e.g. benzoic acid in benzene).
Question 17 of 20
Osmotic pressure is preferred for molar mass of macromolecules because:
it is temperature-independent
it gives measurable values at low concentration
it needs no membrane
it equals molality
Explanation: Even dilute protein solutions give measurable osmotic pressures at room temperature.
Question 18 of 20
The degree of dissociation is $\alpha=$
$\frac{i-1}{n-1}$
$\frac{n-1}{i-1}$
$i(n-1)$
$\frac{1}{i}$
Explanation: $\alpha=\frac{i-1}{n-1}$ for a solute dissociating into $n$ particles.
Question 19 of 20
Molality of a solution containing 1 mol solute in 2 kg solvent is:
0.5 m
1 m
2 m
0.25 m
Explanation: $m=1/2=0.5\ \text{mol kg}^{-1}$.
Question 20 of 20
A larger Henry's constant $K_H$ corresponds to:
a more soluble gas
a less soluble gas
no change in solubility
a solid solute
Explanation: Since $x=p/K_H$, a larger $K_H$ gives lower solubility.