If equilibrium constant for the equation $ A_2 + B_2 \rightleftharpoons 2AB \quad \text{is} \, K_p, $ then find the equilibrium constant for the equation $ AB \rightleftharpoons \frac{1}{2} A_2 + \frac{1}{2} B_2. $
Step 1: Relate the two equilibrium constants.
For the first reaction, the equilibrium constant is given by:
\[ K_p = \frac{[AB]^2}{[A_2][B_2]}. \] Now, for the second reaction: \[ AB \rightleftharpoons \frac{1}{2} A_2 + \frac{1}{2} B_2, \] The equilibrium constant for this reaction, say \( K' \), can be written as: \[ K' = \frac{[A_2]^{1/2} [B_2]^{1/2}}{[AB]}. \]
Step 2: Calculate the relationship between \( K_p \) and \( K' \).
Since the stoichiometry of the second reaction is half of that in the first, the equilibrium constant \( K' \) is related to \( K_p \) as: \[ K' = \frac{1}{\sqrt{K_p}}. \] Thus, the correct answer is \( \frac{1}{\sqrt{K_p}} \).
For the reaction A(g) $\rightleftharpoons$ 2B(g), the backward reaction rate constant is higher than the forward reaction rate constant by a factor of 2500, at 1000 K.
[Given: R = 0.0831 atm $mol^{–1} K^{–1}$]
$K_p$ for the reaction at 1000 K is:
The equilibrium constant for decomposition of $ H_2O $ (g) $ H_2O(g) \rightleftharpoons H_2(g) + \frac{1}{2} O_2(g) \quad (\Delta G^\circ = 92.34 \, \text{kJ mol}^{-1}) $ is $ 8.0 \times 10^{-3} $ at 2300 K and total pressure at equilibrium is 1 bar. Under this condition, the degree of dissociation ($ \alpha $) of water is _____ $\times 10^{-2}$ (nearest integer value). [Assume $ \alpha $ is negligible with respect to 1]