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CHEColligative Properties

Depression of Freezing Point Numericals

A non-volatile solute lowers the freezing point in proportion to molality, the basis for antifreeze use and for cryoscopic molar-mass determination. ISC numericals apply ΔTf=Kfm\Delta T_f = K_f m to find molar mass, the freezing point, the mass of solute, or KfK_f itself.

Freezing-point depression
ΔTf=iKfm=Tf(solvent)−Tf(solution)\Delta T_f = i K_f m = T_f(\text{solvent}) - T_f(\text{solution})
KfK_f cryoscopic constant, mm molality, ii van't Hoff factor
Molar mass from depression
M2=i Kf w2×1000ΔTf×w1M_2 = \dfrac{i \, K_f \, w_2 \times 1000}{\Delta T_f \times w_1}
w2w_2 solute mass (g), w1w_1 solvent mass (g)
Cryoscopic constant from data
Kf=ΔTf×M2×w1w2×1000K_f = \dfrac{\Delta T_f \times M_2 \times w_1}{w_2 \times 1000}
use when the solute molar mass M2M_2 is known (non-electrolyte, i=1i = 1)
  • Depression of freezing point: ΔTf=iKfm\Delta T_f = i K_f m, where KfK_f is the molal (cryoscopic) constant.
  • ΔTf=Tf(pure solvent)−Tf(solution)\Delta T_f = T_f(\text{pure solvent}) - T_f(\text{solution}); for water Kf=1.86 K kg mol−1K_f = 1.86\,\text{K kg mol}^{-1}.
  • Molar mass from depression: M=iKf×w2×1000ΔTf×w1M = \dfrac{i K_f \times w_2 \times 1000}{\Delta T_f \times w_1}, with masses w2w_2 (solute) and w1w_1 (solvent) in grams.
  • Rearranged to find KfK_f for a known non-electrolyte: Kf=ΔTf×M×w1w2×1000K_f = \dfrac{\Delta T_f \times M \times w_1}{w_2 \times 1000}.
  • Mass of solute for a target freezing point: get mm from ΔTf=Kfm\Delta T_f = K_f m, then w=m×(kg solvent)×Mrw = m \times (\text{kg solvent}) \times M_r.
  • Ethylene glycol is the common antifreeze example — a non-electrolyte (i=1i = 1) added to water to lower its freezing point.
  • A solute lowers the freezing point because it reduces the solvent's vapour pressure, so the solid-liquid equilibrium is reached at a lower temperature.
  • KfK_f is the depression for a 1 molal1\,\text{molal} non-electrolyte solution and is a property of the solvent alone, with units K kg mol−1\text{K kg mol}^{-1}.
  • For benzene Kf=5.12 K kg mol−1K_f = 5.12\,\text{K kg mol}^{-1}, larger than water's 1.861.86, so benzene gives bigger, more precisely measured depressions — useful in molar-mass work.
  • Order of solving: find ΔTf\Delta T_f from the two freezing points, then molality, then moles and molar mass (including ii for electrolytes).
  • Freezing-point depression is the basis of antifreeze (ethylene glycol in radiators) and of de-icing roads with salt, which gives a large ΔTf\Delta T_f because of its ii.
  • Trap: a freezing point of −0.372∘C-0.372^\circ\text{C} means ΔTf=0.372 K\Delta T_f = 0.372\,\text{K} (magnitude below 0∘C0^\circ\text{C}), not the temperature itself.
Where the marks go
  • Substituting the negative freezing-point temperature for ΔTf\Delta T_f; the depression is its magnitude below the pure-solvent freezing point.
  • Computing ΔTf\Delta T_f as solution minus solvent; depression is solvent minus solution (a positive value).
  • Forgetting ii for an electrolyte (e.g. de-icing salt), which underestimates the depression.
  • Using water's Kf=1.86K_f = 1.86 when the solvent is benzene (5.125.12) or another liquid — KfK_f is solvent-specific.
  • Unit slip: molality requires solvent mass in kg, while the molar-mass formula keeps w1w_1 in grams with the ×1000\times 1000 factor.
How the board asks it
  • Numericalmolar mass from depression
    On dissolving 1.9 g1.9\,\text{g} of a non-volatile, non-electrolyte solute in 75 g75\,\text{g} of water, the freezing point of the solution is found to be −0.465 ∘C-0.465\,^\circ\text{C}. Calculate the molar mass of the solute (KfK_f for water =1.86 K kg mol−1= 1.86\,\text{K kg mol}^{-1}).
  • Numericalfreezing point from ΔTf=Kfm\Delta T_f = K_f m
    Calculate the freezing point of a solution prepared by dissolving 18 g18\,\text{g} of glucose (M=180 g mol−1M = 180\,\text{g mol}^{-1}) in 250 g250\,\text{g} of water, given Kf=1.86 K kg mol−1K_f = 1.86\,\text{K kg mol}^{-1} for water.
  • Numericalmass of solute for a target freezing point
    What mass of ethylene glycol (M=62 g mol−1M = 62\,\text{g mol}^{-1}) must be added to 5.5 kg5.5\,\text{kg} of water to lower its freezing point to −10 ∘C-10\,^\circ\text{C}? (Kf=1.86 K kg mol−1K_f = 1.86\,\text{K kg mol}^{-1})
  • NumericalKfK_f of solvent from a known non-electrolyte
    A solution of 1.0 g1.0\,\text{g} of a non-electrolyte (M=256 g mol−1M = 256\,\text{g mol}^{-1}) in 50 g50\,\text{g} of benzene freezes 0.40 K0.40\,\text{K} below the freezing point of pure benzene. Calculate the molal depression constant KfK_f of benzene.
  • Numericalvan't Hoff factor and degree of dissociation
    1.0 g1.0\,\text{g} of a strong electrolyte ABAB (M=100 g mol−1M = 100\,\text{g mol}^{-1}) is dissolved in 100 g100\,\text{g} of water and the solution freezes at −0.31 ∘C-0.31\,^\circ\text{C}. Calculate the van't Hoff factor ii and the degree of dissociation (Kf=1.86 K kg mol−1K_f = 1.86\,\text{K kg mol}^{-1}).
  • Numericaldepression as proportional to molality
    Equal masses of urea (M=60 g mol−1M = 60\,\text{g mol}^{-1}) and glucose (M=180 g mol−1M = 180\,\text{g mol}^{-1}) are each dissolved in 100 g100\,\text{g} of water. Calculate the ratio of the freezing-point depressions of the two solutions.

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Written for Sublevo. Question text quoted anywhere in these notes is the Council’s and carries its year and paper; the board’s own diagrams are not reproduced.