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For a reaction taking place in a contain...

For a reaction taking place in a container in equilibrium with its surroundings, the effect of temperature on its equilibrium constant Kin terms of change in entropy is described by

A

With increase in temperature, the value of Kfor exothermic reaction decreases because the entropy change of the system is positive

B

With increase in temperature, the value of Kfor endothermic reaction increases because unfavourable change in entropy of the surroundings decreases

C

With increase in temperature, the value of Kfor endothermic reaction increases because the entropy change of the system is negative

D

With increase in temperature, the value of Kfor exothermic reaction decreases because favourable change in entropy of the surroundings decreases

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To solve the question regarding the effect of temperature on the equilibrium constant (K) in terms of change in entropy (ΔS), we can follow these steps: ### Step 1: Understanding the Relationship Between K and Temperature The equilibrium constant (K) for a reaction is temperature-dependent. The Van 't Hoff equation describes how K changes with temperature. It is given by: \[ \log \left( \frac{K_2}{K_1} \right) = -\frac{\Delta H}{2.303R} \left( \frac{1}{T_2} - \frac{1}{T_1} \right) \] where: - \( K_1 \) and \( K_2 \) are the equilibrium constants at temperatures \( T_1 \) and \( T_2 \) respectively, - \( \Delta H \) is the change in enthalpy, - \( R \) is the universal gas constant. ### Step 2: Analyzing Exothermic Reactions For exothermic reactions, the change in enthalpy (\( \Delta H \)) is negative. According to the Van 't Hoff equation: - If the temperature increases (\( T_2 > T_1 \)), the term \( \frac{1}{T_2} - \frac{1}{T_1} \) becomes negative, making \( \log \left( \frac{K_2}{K_1} \right) \) positive. - This implies that \( K_2 < K_1 \), meaning that the equilibrium constant decreases with an increase in temperature. ### Step 3: Analyzing Endothermic Reactions For endothermic reactions, the change in enthalpy (\( \Delta H \)) is positive. In this case: - If the temperature increases, the term \( \frac{1}{T_2} - \frac{1}{T_1} \) remains positive, making \( \log \left( \frac{K_2}{K_1} \right) \) negative. - This implies that \( K_2 > K_1 \), meaning that the equilibrium constant increases with an increase in temperature. ### Step 4: Relating ΔS to K The change in entropy (\( \Delta S \)) is related to the change in enthalpy and the change in Gibbs free energy (\( \Delta G \)) by the equation: \[ \Delta G = \Delta H - T\Delta S \] At equilibrium, \( \Delta G = 0 \), thus: \[ 0 = \Delta H - T\Delta S \implies \Delta S = \frac{\Delta H}{T} \] ### Step 5: Conclusion - For exothermic reactions, as temperature increases, \( K \) decreases, and the entropy change of the system is negative while that of the surroundings is positive. - For endothermic reactions, as temperature increases, \( K \) increases, and the entropy change of the system is positive while that of the surroundings is negative. ### Summary of Key Points 1. **Exothermic Reactions**: \( K \) decreases with increasing temperature. 2. **Endothermic Reactions**: \( K \) increases with increasing temperature. 3. **Entropy Changes**: The sign of \( \Delta S \) for the system and surroundings varies based on whether the reaction is exothermic or endothermic.
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