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The equilibrium constant for A(g)+B(2)...

The equilibrium constant for
`A(g)+B_(2)(g) hArr AB_(2)(g)" "k_(p)=100` at `522K`.
Structure of `AB_(2)` is like `H_(2)O` . If bond energy of `A-B` bond is `200 kJ//mol` and that of `B-B` bond is `100 kJ//mol,` the find `Delta S^(@)` of the above reaction `:`

A

`-0.53J //mol-K`

B

`-536 J //mol-K`

C

`-550J//mol-K`

D

`-5.36J//mol-K`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to find the standard entropy change (ΔS°) for the reaction: \[ A(g) + B_2(g) \rightleftharpoons AB_2(g) \] Given data: - Equilibrium constant \( K_p = 100 \) at \( 522 \, K \) - Bond energy of \( A-B \) bond = \( 200 \, kJ/mol \) - Bond energy of \( B-B \) bond = \( 100 \, kJ/mol \) ### Step 1: Write the reaction and identify the bonds The reaction is: \[ A(g) + B_2(g) \rightarrow AB_2(g) \] In this reaction: - We break one \( B-B \) bond in \( B_2 \). - We form two \( A-B \) bonds in \( AB_2 \). ### Step 2: Calculate the change in enthalpy (ΔH°) Using the bond energies, we can calculate the change in enthalpy (ΔH°) using the formula: \[ \Delta H° = \text{(Bond energies of reactants)} - \text{(Bond energies of products)} \] For the reactants: - Breaking one \( B-B \) bond: \( +100 \, kJ/mol \) For the products: - Forming two \( A-B \) bonds: \( -2 \times 200 \, kJ/mol = -400 \, kJ/mol \) Thus, we have: \[ \Delta H° = 100 - 400 = -300 \, kJ/mol \] ### Step 3: Calculate the change in Gibbs free energy (ΔG°) Using the equilibrium constant \( K_p \), we can calculate ΔG° using the formula: \[ \Delta G° = -RT \ln K_p \] Where: - \( R = 8.314 \, J/(mol \cdot K) = 0.008314 \, kJ/(mol \cdot K) \) - \( T = 522 \, K \) - \( K_p = 100 \) Calculating: \[ \Delta G° = - (0.008314 \, kJ/(mol \cdot K)) \times (522 \, K) \times \ln(100) \] Using \( \ln(100) = 4.605 \): \[ \Delta G° = - (0.008314 \times 522 \times 4.605) \approx -19.99 \, kJ/mol \] ### Step 4: Calculate the standard entropy change (ΔS°) Using the relationship between ΔG°, ΔH°, and ΔS°: \[ \Delta G° = \Delta H° - T \Delta S° \] Rearranging gives: \[ \Delta S° = \frac{\Delta H° - \Delta G°}{T} \] Substituting the values: \[ \Delta S° = \frac{-300 \, kJ/mol - (-19.99 \, kJ/mol)}{522 \, K} \] \[ \Delta S° = \frac{-300 + 19.99}{522} = \frac{-280.01}{522} \approx -0.536 \, kJ/(mol \cdot K) \] Converting to Joules: \[ \Delta S° \approx -536 \, J/(mol \cdot K) \] ### Final Answer: The standard entropy change (ΔS°) for the reaction is approximately: \[ \Delta S° = -536 \, J/(mol \cdot K) \]

To solve the problem, we need to find the standard entropy change (ΔS°) for the reaction: \[ A(g) + B_2(g) \rightleftharpoons AB_2(g) \] Given data: - Equilibrium constant \( K_p = 100 \) at \( 522 \, K \) - Bond energy of \( A-B \) bond = \( 200 \, kJ/mol \) - Bond energy of \( B-B \) bond = \( 100 \, kJ/mol \) ...
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