We can use the formula for freezing point depression to calculate the lowering in vapour pressure. The formula is:
\[
\Delta T_f = \frac{K_f \cdot m}{1000}
\]
where:
\(\Delta T_f\) is the freezing point depression,
\(K_f\) is the cryoscopic constant (1.86 K kg mol\(^{-1}\) for water),
and \(m\) is the molality of the solution.
Since the solution freezes at -0.3°C, the freezing point depression \(\Delta T_f = 0.3\) K. Using the equation for freezing point depression, we can solve for \(m\), the molality of the solution.
\[
m = \frac{\Delta T_f \cdot 1000}{K_f} = \frac{0.3 \cdot 1000}{1.86} = 161.29 \, \text{mol/kg}
\]
Next, the lowering of vapour pressure is given by Raoult's Law:
\[
\frac{\Delta P}{P_0} = m \cdot X_1
\]
where \(X_1\) is the mole fraction of the solvent (water) and \(P_0\) is the vapour pressure of pure water. Since the molality of the solution is high, we can estimate the lowering of vapour pressure by the formula:
\[
\Delta P = P_0 \cdot \left( \frac{m}{1000} \right)
\]
Substituting the values:
\[
\Delta P = 24.8 \cdot \left( \frac{161.29}{1000} \right) = 4.0 \, \text{mm Hg}
\]
Therefore, the lowering in vapour pressure is 4.0 mm Hg.