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Van't Hoff's equation for a chemical rea...

Van't Hoff's equation for a chemical reaction under equilibrium is given by standard reaction enthalpy at temperature T and K is the equilibrium constant . Predict how K will vary with temperature for an exothermic

A

K decreases as the temperature rises

B

K is remain unchanged

C

K increases as the temperature rise

D

Information is not sufficient

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To solve the problem regarding how the equilibrium constant \( K \) varies with temperature for an exothermic reaction, we can follow these steps: ### Step-by-Step Solution: 1. **Understand Van't Hoff's Equation**: Van't Hoff's equation relates the change in the equilibrium constant \( K \) with temperature \( T \) and the standard reaction enthalpy \( \Delta H \). The equation is given by: \[ \log\left(\frac{K_1}{K_2}\right) = -\frac{\Delta H}{R} \left(\frac{1}{T_2} - \frac{1}{T_1}\right) \] where \( R \) is the universal gas constant. 2. **Identify the Nature of the Reaction**: For an exothermic reaction, the standard reaction enthalpy \( \Delta H \) is negative (\( \Delta H < 0 \)). 3. **Consider Two Temperatures**: Let’s consider two temperatures, \( T_1 \) and \( T_2 \), where \( T_2 > T_1 \). 4. **Analyze the Equation**: Since \( \Delta H \) is negative, the right side of the equation becomes positive when \( T_2 > T_1 \): \[ \log\left(\frac{K_1}{K_2}\right) = -\frac{\Delta H}{R} \left(\frac{1}{T_2} - \frac{1}{T_1}\right) > 0 \] This implies that: \[ K_1 > K_2 \] 5. **Interpret the Results**: Since \( K_1 > K_2 \) and \( T_2 > T_1 \), it indicates that as the temperature increases, the equilibrium constant \( K \) decreases for an exothermic reaction. 6. **Conclusion**: Therefore, we conclude that for an exothermic reaction, the equilibrium constant \( K \) decreases as the temperature increases. ### Final Answer: For an exothermic reaction, the equilibrium constant \( K \) decreases with an increase in temperature.
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Effect of temperature on the equilibrium process analysed by using the thermodynamics From the thermodynamics reaction DeltaG^(@)=-2.30RTlogk DeltaG^(@): Standing free energy change DeltaG^(@)=DeltaH^(@)-TDeltaS^(@) …(ii) DeltaH^(@) : Standard heat of the reaction gt From eqns.(i) and(ii) -2RTlogk=DeltaH^(@)=TDeltaS^(@) DeltaS^(@) : standard entropy change implies" "logK=-(DeltaH^(@))/(2.3RT)+(DeltaS^(@))/(2.3R) Clearly, if a plot of k vs 1/T is made then it is a straight lone having slope =(-DeltaH^(@))/(2.3R) amd y intercept =(DeltaS^(@))/(2.3R) If at temperature T_(1) equilibrium constant be k_(1) and at temperature T_(2) equilibrium constant be k_(2) then : implies" "logK_(1)=-(DeltaH^(@))/(2.3RT_(1))+(DeltaS^(@))/(2.3R) ..(iv) implies" "logK_(2)=-(DeltaH^(@))/(2.3RT_(2))+(DeltaS^(@))/(2.3R) ...(v) Substracting e.q (iv) from (v), we get from the relation we can conclude that the of equilibrium constant increase in temperature for endothermic reaction eith but value of equilibrium constant decrease with the increase in temperature for exothermic reaction For exothermic reaction if DeltaS^(@)lt0 then the sketch of log k vs (1)/(T) may be

Effect of temperature on the equilibrium process analysed by using the thermodynamics From the thermodynamics reaction DeltaG^(@)=-2.30RTlogk DeltaG^(@): Standing free energy change DeltaG^(@)=DeltaH^(@)-TDeltaS^(@) …(ii) DeltaH^(@) : Standard heat of the reaction gt From eqns.(i) and(ii) -2RTlogk=DeltaH^(@)=TDeltaS^(@) DeltaS^(@) : standard entropy change implies" "logK=-(DeltaH^(@))/(2.3RT)+(DeltaS^(@))/(2.3R) Clearly, if a plot of k vs 1/T is made then it is a straight lone having slope =(-DeltaH^(@))/(2.3R) amd y intercept =(DeltaS^(@))/(2.3R) If at temperature T_(1) equilibrium constant be k_(1) and at temperature T_(2) equilibrium constant be k_(2) then : implies" "logK_(1)=-(DeltaH^(@))/(2.3RT_(1))+(DeltaS^(@))/(2.3R) ..(iv) implies" "logK_(2)=-(DeltaH^(@))/(2.3RT_(2))+(DeltaS^(@))/(2.3R) ...(v) Substracting e.q (iv) from (v), we get from the relation we can conclude that the of equilibrium constant increase in temperature for endothermic reaction eith but value of equilibrium constant decrease with the increase in temperature for exothermic reaction If for a particular reversible reaction K_(C)=57 abd 355^(@)C and K_(C)=69 at 450^(@)C then