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For the reaction at 298 k, A(g) +B(g)...

For the reaction at 298 k,
`A(g) +B(g) hArr C(g) +D(g)`
`DeltaH_0=-29.8 kcal, DeltaS^@=-0.100 kcal K^(-1)`
Find the value of equilibrium constant at the same temp.

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To find the equilibrium constant \( K \) for the reaction \( A(g) + B(g) \rightleftharpoons C(g) + D(g) \) at 298 K, we can use the relationship between Gibbs free energy change (\( \Delta G \)), enthalpy change (\( \Delta H \)), and entropy change (\( \Delta S \)). Here are the steps to solve the problem: ### Step 1: Write the Gibbs Free Energy Equation The Gibbs free energy change at standard conditions is given by: \[ \Delta G^\circ = \Delta H^\circ - T \Delta S^\circ \] ### Step 2: Substitute Given Values We know: - \( \Delta H^\circ = -29.8 \, \text{kcal} \) - \( \Delta S^\circ = -0.100 \, \text{kcal K}^{-1} \) - \( T = 298 \, \text{K} \) Substituting these values into the Gibbs free energy equation: \[ \Delta G^\circ = -29.8 \, \text{kcal} - (298 \, \text{K}) \times (-0.100 \, \text{kcal K}^{-1}) \] ### Step 3: Calculate the Entropy Contribution Calculate the entropy contribution: \[ 298 \times (-0.100) = -29.8 \, \text{kcal} \] ### Step 4: Calculate \( \Delta G^\circ \) Now substituting back: \[ \Delta G^\circ = -29.8 + 29.8 = 0 \, \text{kcal} \] ### Step 5: Relate \( \Delta G^\circ \) to the Equilibrium Constant We know that: \[ \Delta G^\circ = -2.303 RT \log K \] Where \( R \) is the gas constant. In kcal, \( R = 0.001987 \, \text{kcal K}^{-1} \text{mol}^{-1} \). ### Step 6: Substitute \( \Delta G^\circ \) into the Equation Since \( \Delta G^\circ = 0 \): \[ 0 = -2.303 \times (0.001987) \times (298) \log K \] ### Step 7: Solve for \( K \) Since the left side is zero, we have: \[ \log K = 0 \] This implies: \[ K = 10^0 = 1 \] ### Final Answer The equilibrium constant \( K \) at 298 K is: \[ K = 1 \]
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