To establish the relationship between the degree of dissociation, denoted by \(x\), of \(X_2Y(g)\) and its equilibrium constant, \(K_p\), we must first examine the provided reaction: \(X_2Y(g) \rightleftharpoons X_2(g) + \frac{1}{2} Y_2(g)\).
- Assume the initial pressure of \(X_2Y(g)\) is \(p\).
- At equilibrium, if the degree of dissociation of \(X_2Y(g)\) is \(x\), the corresponding equilibrium pressures are:
- For \(X_2Y(g)\): \(p(1-x)\)
- For \(X_2(g)\): \(px\)
- For \(\frac{1}{2} Y_2(g)\): \(\frac{px}{2}\)
- The total equilibrium pressure, \(P_T\), can be calculated as:
- \(P_T = p(1-x) + px + \frac{px}{2} = p(1 + \frac{x}{2})\)
- The equilibrium constant, \(K_p\), is defined by the equation:
- \(K_p = \frac{(P_{X_2})(P_{\frac{1}{2}Y_2})}{P_{X_2Y}}\)
- Substituting the equilibrium pressures yields:
- \(K_p = \frac{(px)(\frac{px}{2})}{p(1-x)}\)
- \(K_p = \frac{p^2 x^2 }{2p(1-x)}\)
- Rearranging the expression to solve for \(x\):
- \(K_p = \frac{px^2}{2(1-x)}\)
- Under the assumption that \(x\) is small, \(1 - x \approx 1\).
- \(K_p = \frac{px^2}{2}\)
- Solving for \(x\) produces:
- \(x = \sqrt{\frac{2K_p}{p}}\)
- Therefore, the established relationship between \(x\) and \(K_p\) is:
- \(x = \sqrt{\frac{2K_p}{p}}\)
This derivation confirms that the correct answer is the equation \(x = \sqrt{\frac{2K_p}{p}}\).