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Show that Kp for the reaction, 2H2S(g)...

Show that `K_p` for the reaction,
`2H_2S(g) hArr 2H_2(g) +S_2(g)` is given by the expression
`K_p=(alpha^3P)/((2+alpha)(1-alpha)^2)`
where `alpha` is the degree of dissociation and P is the total equilibrium pressure. Calculate `K_c` of the reaction if `alpha` at 298 k and 1 atm . pressure is 0.055.

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The correct Answer is:
To solve the problem, we need to derive the expression for \( K_p \) for the reaction: \[ 2H_2S(g) \rightleftharpoons 2H_2(g) + S_2(g) \] ### Step 1: Define the degree of dissociation Let \( \alpha \) be the degree of dissociation of \( H_2S \). If we start with 1 mole of \( H_2S \), then at equilibrium: - Moles of \( H_2S \) remaining = \( 1 - \alpha \) - Moles of \( H_2 \) produced = \( 2\alpha \) - Moles of \( S_2 \) produced = \( \alpha \) ### Step 2: Calculate total moles at equilibrium The total number of moles at equilibrium \( n_{total} \) is given by: \[ n_{total} = (1 - \alpha) + 2\alpha + \alpha = 1 + 2\alpha \] ### Step 3: Calculate partial pressures The total pressure \( P \) is given, and the partial pressures can be expressed as: - Partial pressure of \( H_2S \) = \( P_{H_2S} = \frac{(1 - \alpha)P}{(1 + 2\alpha)} \) - Partial pressure of \( H_2 \) = \( P_{H_2} = \frac{2\alpha P}{(1 + 2\alpha)} \) - Partial pressure of \( S_2 \) = \( P_{S_2} = \frac{\alpha P}{(1 + 2\alpha)} \) ### Step 4: Write the expression for \( K_p \) The expression for \( K_p \) is given by: \[ K_p = \frac{(P_{H_2})^2 \cdot (P_{S_2})}{(P_{H_2S})^2} \] Substituting the partial pressures: \[ K_p = \frac{\left(\frac{2\alpha P}{(1 + 2\alpha)}\right)^2 \cdot \left(\frac{\alpha P}{(1 + 2\alpha)}\right)}{\left(\frac{(1 - \alpha)P}{(1 + 2\alpha)}\right)^2} \] ### Step 5: Simplify the expression After substituting and simplifying: \[ K_p = \frac{(4\alpha^2 P^2) \cdot (\alpha P)}{(1 - \alpha)^2 \cdot P^2} \cdot \frac{(1 + 2\alpha)^2}{(1 + 2\alpha)^2} \] This simplifies to: \[ K_p = \frac{4\alpha^3 P}{(1 - \alpha)^2 (1 + 2\alpha)} \] ### Step 6: Final expression for \( K_p \) The final expression for \( K_p \) is: \[ K_p = \frac{\alpha^3 P}{(2 + \alpha)(1 - \alpha)^2} \] ### Step 7: Calculate \( K_c \) Using the relation \( K_p = K_c (RT)^{\Delta n} \): - Calculate \( \Delta n \): \[ \Delta n = n_p - n_r = (2 + 1) - 2 = 1 \] - Therefore, \( K_c = \frac{K_p}{RT} \). ### Step 8: Substitute values Given: - \( \alpha = 0.055 \) - \( P = 1 \, atm \) - \( R = 0.082 \, L \cdot atm/(K \cdot mol) \) - \( T = 298 \, K \) First, calculate \( K_p \): \[ K_p = \frac{(0.055)^3 \cdot 1}{(2 + 0.055)(1 - 0.055)^2} \] Calculating this gives: \[ K_p \approx 9.066 \times 10^{-5} \] Now calculate \( K_c \): \[ K_c = \frac{9.066 \times 10^{-5}}{0.082 \cdot 298} \] Calculating this gives: \[ K_c \approx 3.71 \times 10^{-6} \, mol/L \] ### Final Answer Thus, the value of \( K_c \) is approximately \( 3.71 \times 10^{-6} \, mol/L \).
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