C. Consider a chemical reaction. At a temperature T1 enthalpy of reaction is A,H(T,, P) = 400. J and the Gibbs potential of reaction is A, G(T,,P) 100.J. 300. K and an external pressure P, the
C. Consider a chemical reaction. At a temperature T1 enthalpy of reaction is A,H(T,, P) = 400. J and the Gibbs potential of reaction is A, G(T,,P) 100.J. 300. K and an external pressure P, the
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Is the reaction endothermic or exothermic? Is the forward or backward reaction favorable under these conditions?
![**Chemical Reactions and Thermodynamics**
**Consider a chemical reaction.** At a temperature \( T_1 = 300. \, \text{K} \) and an external pressure \( P \), the enthalpy of reaction is \( \Delta_r H(T_1, P) = 400. \, \text{J} \) and the Gibbs potential of reaction is \( \Delta_r G(T_1, P) = 100. \, \text{J} \).
We will prove later that the Gibbs-Helmholtz relation can also be extended to describe chemical reactions:
\[
\left( \frac{\partial}{\partial T} \left( \frac{\Delta_r G}{T} \right) \right)_P = -\frac{\Delta_r H}{T^2}.
\]
Assuming this relation to hold true, consider the following:
---
**Explanation of the Gibbs-Helmholtz Relation in Chemical Reactions:**
The Gibbs-Helmholtz equation connects changes in temperature to changes in Gibbs energy divided by temperature, under constant pressure. It provides an approach to quantify how the Gibbs free energy of a reaction varies with temperature, taking the enthalpy change into account. This is important for understanding the temperature dependence of reaction spontaneity.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F37df213a-2c14-4822-a979-37f159717cfc%2Fa75953c9-6c38-483f-ab15-8349b2c930da%2Fqj5pnqh_processed.png&w=3840&q=75)
Transcribed Image Text:**Chemical Reactions and Thermodynamics**
**Consider a chemical reaction.** At a temperature \( T_1 = 300. \, \text{K} \) and an external pressure \( P \), the enthalpy of reaction is \( \Delta_r H(T_1, P) = 400. \, \text{J} \) and the Gibbs potential of reaction is \( \Delta_r G(T_1, P) = 100. \, \text{J} \).
We will prove later that the Gibbs-Helmholtz relation can also be extended to describe chemical reactions:
\[
\left( \frac{\partial}{\partial T} \left( \frac{\Delta_r G}{T} \right) \right)_P = -\frac{\Delta_r H}{T^2}.
\]
Assuming this relation to hold true, consider the following:
---
**Explanation of the Gibbs-Helmholtz Relation in Chemical Reactions:**
The Gibbs-Helmholtz equation connects changes in temperature to changes in Gibbs energy divided by temperature, under constant pressure. It provides an approach to quantify how the Gibbs free energy of a reaction varies with temperature, taking the enthalpy change into account. This is important for understanding the temperature dependence of reaction spontaneity.
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By studying the temperature, enthalpy, and Gibbs free energy we can conclude that if the reaction is exothermic or endothermic and forward or backward in nature.
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