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The degree of dissociation of SO(3) is a...

The degree of dissociation of `SO_(3)` is `alpha` at equilibrium pressure `P_(0)`.
`K_(P)` for `2SO_(3)(g)hArr2SO_(2)(g)+O_(2)(g)`is

A

`[(P_(0)alpha^(3))//2(1-alpha)^(3)]`

B

`[(P_(0)alpha^(3))//(2+alpha)(1-alpha)^(2)]`

C

`[(P_(0)alpha^(2))//2(1-alpha)^(2)]`

D

None of these

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The correct Answer is:
To find the equilibrium constant \( K_p \) for the reaction \[ 2 \text{SO}_3(g) \rightleftharpoons 2 \text{SO}_2(g) + \text{O}_2(g) \] given that the degree of dissociation of \( \text{SO}_3 \) is \( \alpha \) at equilibrium pressure \( P_0 \), we can follow these steps: ### Step 1: Write the Initial and Equilibrium Conditions Assume we start with 2 moles of \( \text{SO}_3 \). At equilibrium, the degree of dissociation \( \alpha \) indicates how much of \( \text{SO}_3 \) has dissociated. - **Initial moles:** - \( \text{SO}_3 = 2 \) - \( \text{SO}_2 = 0 \) - \( \text{O}_2 = 0 \) - **Change in moles:** - \( \text{SO}_3 \) dissociates: \( -2\alpha \) - \( \text{SO}_2 \) forms: \( +2\alpha \) - \( \text{O}_2 \) forms: \( +\alpha \) - **Equilibrium moles:** - \( \text{SO}_3 = 2 - 2\alpha \) - \( \text{SO}_2 = 2\alpha \) - \( \text{O}_2 = \alpha \) ### Step 2: Calculate Total Moles at Equilibrium The total moles at equilibrium can be calculated as: \[ \text{Total moles} = (2 - 2\alpha) + (2\alpha) + \alpha = 2 + \alpha \] ### Step 3: Determine Partial Pressures The partial pressures of each species can be expressed in terms of the total pressure \( P_0 \): - **Partial pressure of \( \text{SO}_3 \):** \[ P_{\text{SO}_3} = \left(\frac{2 - 2\alpha}{2 + \alpha}\right) P_0 \] - **Partial pressure of \( \text{SO}_2 \):** \[ P_{\text{SO}_2} = \left(\frac{2\alpha}{2 + \alpha}\right) P_0 \] - **Partial pressure of \( \text{O}_2 \):** \[ P_{\text{O}_2} = \left(\frac{\alpha}{2 + \alpha}\right) P_0 \] ### Step 4: Write the Expression for \( K_p \) The equilibrium constant \( K_p \) is given by the expression: \[ K_p = \frac{(P_{\text{SO}_2})^2 \cdot P_{\text{O}_2}}{(P_{\text{SO}_3})^2} \] Substituting the partial pressures we calculated: \[ K_p = \frac{\left(\left(\frac{2\alpha}{2 + \alpha}\right) P_0\right)^2 \cdot \left(\frac{\alpha}{2 + \alpha}\right) P_0}{\left(\left(\frac{2 - 2\alpha}{2 + \alpha}\right) P_0\right)^2} \] ### Step 5: Simplify the Expression Now, simplifying the expression: \[ K_p = \frac{\left(\frac{4\alpha^2}{(2 + \alpha)^2} P_0^2\right) \cdot \left(\frac{\alpha}{2 + \alpha}\right) P_0}{\left(\frac{(2 - 2\alpha)^2}{(2 + \alpha)^2} P_0^2\right)} \] This simplifies to: \[ K_p = \frac{4\alpha^3 P_0}{(2 - 2\alpha)^2} \cdot \frac{(2 + \alpha)^2}{(2 + \alpha)^2} \] The \( P_0^2 \) cancels out, leading to: \[ K_p = \frac{4\alpha^3 P_0}{(2 - 2\alpha)^2} \] ### Step 6: Final Expression for \( K_p \) Thus, the final expression for \( K_p \) is: \[ K_p = \frac{P_0 \alpha^3}{(2 + \alpha)(1 - \alpha)^2} \]

To find the equilibrium constant \( K_p \) for the reaction \[ 2 \text{SO}_3(g) \rightleftharpoons 2 \text{SO}_2(g) + \text{O}_2(g) \] given that the degree of dissociation of \( \text{SO}_3 \) is \( \alpha \) at equilibrium pressure \( P_0 \), we can follow these steps: ...
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