C. Consider a chemical reaction. At a temperature T1 = 300. K and an external pressure P, the enthalpy of reaction is A„H(T,, P) = 400.J and the Gibbs potential of reaction is A, G(T,, P) = 100. J. We will prove later that Gibbs-Helmholtz relation can also extended to describe chemical reactions ( ). ArH *. Assuming this relation to hold true, consider the following: T

Introduction to Chemical Engineering Thermodynamics
8th Edition
ISBN:9781259696527
Author:J.M. Smith Termodinamica en ingenieria quimica, Hendrick C Van Ness, Michael Abbott, Mark Swihart
Publisher:J.M. Smith Termodinamica en ingenieria quimica, Hendrick C Van Ness, Michael Abbott, Mark Swihart
Chapter1: Introduction
Section: Chapter Questions
Problem 1.1P
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Assuming that deltarH is independent of temperature, estimate the temperature at which the forward reaction is favorable. 

### Thermodynamic Concepts in Chemical Reactions

**Consideration of a Chemical Reaction:**

At a temperature \( T_1 = 300.\,\text{K} \) and an external pressure \( P \), the enthalpy of reaction is given by:

\[ \Delta_r H(T_1, P) = 400.\,\text{J} \]

Additionally, the Gibbs potential of the reaction is:

\[ \Delta_r G(T_1, P) = 100.\,\text{J} \]

**Extension of Gibbs-Helmholtz Relation:**

We will prove later that the Gibbs-Helmholtz relation can also be extended to describe chemical reactions. The relation is expressed as:

\[
\left( \frac{\partial}{\partial T} \left( \frac{\Delta_r G}{T} \right) \right)_P = -\frac{\Delta_r H}{T^2}
\]

Assuming this relation to hold true, we can make further considerations.
Transcribed Image Text:### Thermodynamic Concepts in Chemical Reactions **Consideration of a Chemical Reaction:** At a temperature \( T_1 = 300.\,\text{K} \) and an external pressure \( P \), the enthalpy of reaction is given by: \[ \Delta_r H(T_1, P) = 400.\,\text{J} \] Additionally, the Gibbs potential of the reaction is: \[ \Delta_r G(T_1, P) = 100.\,\text{J} \] **Extension of Gibbs-Helmholtz Relation:** We will prove later that the Gibbs-Helmholtz relation can also be extended to describe chemical reactions. The relation is expressed as: \[ \left( \frac{\partial}{\partial T} \left( \frac{\Delta_r G}{T} \right) \right)_P = -\frac{\Delta_r H}{T^2} \] Assuming this relation to hold true, we can make further considerations.
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