For an ideal solution, the total vapour pressure is given by Raoult's Law: \[ P_{\text{total}} = P_X + P_Y \] where \(P_X\) and \(P_Y\) are the partial vapour pressures of components X and Y, respectively. The partial vapour pressure of a component in a solution is given by: \[ P_X = X_X \times P_X^0 \quad \text{and} \quad P_Y = X_Y \times P_Y^0 \] where \(X_X\) and \(X_Y\) are the mole fractions of X and Y, and \(P_X^0\) and \(P_Y^0\) are the vapour pressures of pure X and Y. Given:
The vapour pressure of pure X, \(P_X^0 = 200\) mm Hg.
The vapour pressure of pure Y, \(P_Y^0 = 300\) mm Hg.
The mole ratio of X and Y is 3:2,
so: \[ X_X = \frac{3}{3+2} = \frac{3}{5} \quad \text{and} \quad X_Y = \frac{2}{3+2} = \frac{2}{5} \]
Now, calculate the partial pressures: \[ P_X = \frac{3}{5} \times 200 = 120 \, \text{mm Hg} \] \[ P_Y = \frac{2}{5} \times 300 = 120 \, \text{mm Hg} \] Thus, the total vapour pressure is: \[ P_{\text{total}} = 120 + 120 = 240 \, \text{mm Hg} \]
The correct option is (D) : \(240\)
According to Raoult's Law, the vapor pressure of an ideal solution is given by:
p_total = p_X + p_Y
where:
p_X = X_X * p_X^0 (vapor pressure of component X in the solution)
p_Y = X_Y * p_Y^0 (vapor pressure of component Y in the solution)
Here, \(X_X\) and \(X_Y\) are the mole fractions of X and Y, respectively, and \(p_X^0\) and \(p_Y^0\) are the vapor pressures of the pure components.
Given: - Vapor pressure of pure X (\(p_X^0\)) = 200 mm of Hg - Vapor pressure of pure Y (\(p_Y^0\)) = 300 mm of Hg - Mole ratio of X and Y = 3:2, hence:
- Mole fraction of X, \(X_X = \frac{3}{3+2} = \frac{3}{5} = 0.6\)
- Mole fraction of Y, \(X_Y = \frac{2}{3+2} = \frac{2}{5} = 0.4\) Now, applying Raoult's Law:
p_total = (0.6 * 200) + (0.4 * 300)
p_total = 120 + 120 = 240 mm of Hg
Therefore, the correct vapor pressure of the solution is 240 mm of Hg.