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) : \(240\)
For the reaction:
\[ 2A + B \rightarrow 2C + D \]
The following kinetic data were obtained for three different experiments performed at the same temperature:
\[ \begin{array}{|c|c|c|c|} \hline \text{Experiment} & [A]_0 \, (\text{M}) & [B]_0 \, (\text{M}) & \text{Initial rate} \, (\text{M/s}) \\ \hline I & 0.10 & 0.10 & 0.10 \\ II & 0.20 & 0.10 & 0.40 \\ III & 0.20 & 0.20 & 0.40 \\ \hline \end{array} \]
The total order and order in [B] for the reaction are respectively: