\( \frac{2 K_p}{p} \)
$\sqrt[3]{\frac{2 K_p^2}{p}}$
To solve this problem, we need to find the degree of dissociation, $x$, in terms of the equilibrium constant $K_p$ and the total pressure $p$ for the given reaction.
1. Understanding the Equilibrium:
The reaction is: $AB_{2(g)} \rightleftharpoons AB_{(g)} + \frac{1}{2} B_{2(g)}$. We will use an ICE table to relate the initial pressure, the change in pressure due to dissociation, and the equilibrium pressures.
2. Setting Up the ICE Table:
Assume initial pressure of $AB_2$ is $p_0$.
| | $AB_{2(g)}$ | $AB_{(g)}$ | $B_{2(g)}$ | | :---------- | :---------- | :-------- | :---------------- | | Initial | $p_0$ | $0$ | $0$ | | Change | $-xp_0$ | $+xp_0$ | $+\frac{1}{2}xp_0$ | | Equilibrium | $p_0(1-x)$ | $xp_0$ | $\frac{1}{2}xp_0$ |
3. Total Pressure at Equilibrium:
The total pressure $p$ is the sum of the partial pressures at equilibrium:
$p = p_0(1-x) + xp_0 + \frac{1}{2}xp_0 = p_0(1 + \frac{1}{2}x)$
Since $x \ll 1$, $p \approx p_0$.
4. Expressing $K_p$ in Terms of Partial Pressures:
$K_p = \frac{P_{AB} \cdot (P_{B_2})^{1/2}}{P_{AB_2}} = \frac{(xp_0) \cdot (\frac{1}{2}xp_0)^{1/2}}{p_0(1-x)}$
5. Simplifying the Expression:
Since $x \ll 1$, we can approximate $(1-x) \approx 1$:
$K_p \approx \frac{(xp_0) \cdot (\frac{1}{\sqrt{2}}\sqrt{x}\sqrt{p_0})}{p_0} = \frac{x^{3/2}p_0^{3/2}}{\sqrt{2}p_0} = \frac{x^{3/2}\sqrt{p_0}}{\sqrt{2}}$
Since $p \approx p_0$, $K_p \approx \frac{x^{3/2}\sqrt{p}}{\sqrt{2}}$.
6. Solving for $x$:
$x^{3/2} = \frac{\sqrt{2}K_p}{\sqrt{p}}$
$x = \left(\frac{\sqrt{2}K_p}{\sqrt{p}}\right)^{2/3} = \left(\frac{2K_p^2}{p}\right)^{1/3} = \sqrt[3]{\frac{2K_p^2}{p}}$
Final Answer:
The degree of dissociation $x$ is $\sqrt[3]{\frac{2 K_p^2}{p}}$.
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The reaction : \(A_2 \rightleftharpoons 2A\)

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What will be the equilibrium constant of the given reaction carried out in a \(5 \,L\) vessel and having equilibrium amounts of \(A_2\) and \(A\) as \(0.5\) mole and \(2 \times 10^{-6}\) mole respectively?
The reaction : \(A_2 \rightleftharpoons 2A\)
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