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For the reaction,SO(2)(g)+1//2O(2)(g)hAr...

For the reaction,`SO_(2)(g)+1//2O_(2)(g)hArrSO_(3)(g)`
`DeltaH_(298)^(@)=-98.32KJ//mol e,DeltaS_(298)^(@)=-95.0J//mol e-K`. Find the `K_(p)` for this reaction at `298K. `

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To find the equilibrium constant \( K_p \) for the reaction \[ SO_2(g) + \frac{1}{2} O_2(g) \rightleftharpoons SO_3(g) \] at 298 K, we will use the Gibbs free energy change (\( \Delta G^\circ \)) and its relation to \( K_p \). ### Step-by-step Solution: 1. **Identify the Given Values**: - \( \Delta H^\circ_{298} = -98.32 \, \text{kJ/mol} \) - \( \Delta S^\circ_{298} = -95.0 \, \text{J/mol K} \) 2. **Convert \( \Delta H^\circ \) to Joules**: Since \( \Delta H^\circ \) is given in kJ, we convert it to J: \[ \Delta H^\circ = -98.32 \, \text{kJ/mol} \times 1000 \, \text{J/kJ} = -98320 \, \text{J/mol} \] 3. **Use the Gibbs Free Energy Equation**: The Gibbs free energy change is given by: \[ \Delta G^\circ = \Delta H^\circ - T \Delta S^\circ \] Plugging in the values: \[ \Delta G^\circ = -98320 \, \text{J/mol} - 298 \, \text{K} \times (-95.0 \, \text{J/mol K}) \] 4. **Calculate \( T \Delta S^\circ \)**: \[ T \Delta S^\circ = 298 \times (-95.0) = -28310 \, \text{J/mol} \] 5. **Calculate \( \Delta G^\circ \)**: \[ \Delta G^\circ = -98320 + 28310 = -70010 \, \text{J/mol} \] 6. **Relate \( \Delta G^\circ \) to \( K_p \)**: The relationship between \( \Delta G^\circ \) and \( K_p \) is given by: \[ \Delta G^\circ = -RT \ln K_p \] Rearranging gives: \[ \ln K_p = -\frac{\Delta G^\circ}{RT} \] 7. **Substituting Values**: Using \( R = 8.314 \, \text{J/mol K} \) and \( T = 298 \, \text{K} \): \[ \ln K_p = -\frac{-70010}{8.314 \times 298} \] 8. **Calculate \( \ln K_p \)**: \[ \ln K_p = \frac{70010}{2477.572} \approx 28.24 \] 9. **Calculate \( K_p \)**: To find \( K_p \), we take the exponential: \[ K_p = e^{28.24} \approx 1.8 \times 10^{12} \] ### Final Answer: \[ K_p \approx 1.8 \times 10^{12} \]
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