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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

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The correct Answer is:
To determine how the equilibrium constant \( K \) varies with temperature for an exothermic reaction, we can use Van't Hoff's equation, which relates the change in the equilibrium constant with temperature to the standard reaction enthalpy and entropy. ### Step-by-Step Solution: 1. **Understand Van't Hoff's Equation**: The Van't Hoff equation is given by: \[ \ln K = -\frac{\Delta H^\circ}{R} \cdot \frac{1}{T} + \frac{\Delta S^\circ}{R} \] where: - \( K \) is the equilibrium constant, - \( \Delta H^\circ \) is the standard reaction enthalpy, - \( R \) is the universal gas constant, - \( T \) is the temperature in Kelvin, - \( \Delta S^\circ \) is the standard reaction entropy. 2. **Identify the Nature of the Reaction**: For an exothermic reaction, the standard reaction enthalpy \( \Delta H^\circ \) is negative (i.e., \( \Delta H^\circ < 0 \)). 3. **Analyze the Equation**: Since \( \Delta H^\circ \) is negative, the term \(-\frac{\Delta H^\circ}{R}\) becomes positive. This means that the slope of the line when plotting \( \ln K \) against \( \frac{1}{T} \) is positive. 4. **Graphical Interpretation**: - On the graph, as \( T \) increases, \( \frac{1}{T} \) decreases. - Since \( \ln K \) is positively correlated with \( \frac{1}{T} \), an increase in \( T \) (which decreases \( \frac{1}{T} \)) will lead to a decrease in \( \ln K \). 5. **Conclude the Effect on \( K \)**: If \( \ln K \) decreases, then \( K \) itself must also decrease. Therefore, for an exothermic reaction, as the temperature increases, the equilibrium constant \( K \) decreases. ### Final Answer: For an exothermic reaction, the equilibrium constant \( K \) decreases as the temperature rises.
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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

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