Decomposition of N2O5 Entropy Equilibrium

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SUMMARY

The discussion focuses on the entropy equilibrium of the decomposition of N2O5, specifically addressing the calculation of equilibrium constants (Kp) and Gibbs free energy (DG). The formula derived for Kp is (1+x)(4x)^4/(1-2x)^2, with a calculated DGnaught of 28058 J and a DS of 258 mol/K. The reaction is confirmed to be endothermic, and temperature increases favor the forward reaction. The calculated Kp values at 298K and 345K are 5.29x10^34 and 8.61x10^29, respectively.

PREREQUISITES
  • Understanding of chemical equilibrium and Kp calculations
  • Familiarity with Gibbs free energy and its relation to reaction spontaneity
  • Knowledge of the Clausius-Clapeyron equation for temperature dependence of Kp
  • Basic algebraic manipulation skills for solving equations
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  • Study the derivation and application of the Clausius-Clapeyron equation
  • Learn about the relationship between Gibbs free energy and equilibrium constants
  • Explore advanced techniques for solving nonlinear equations in chemical equilibria
  • Investigate the effects of temperature on reaction kinetics and equilibrium
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Chemistry students, researchers in thermodynamics, and professionals working with chemical equilibria and reaction kinetics will benefit from this discussion.

yolo123
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Please see attached picture.
I need verification of my answers. I unfortunately found these problems on an old book with no answer. I would really appreciate it.

(a) Ok. For this one, I am really not sure. PLEASE help.
I get a very complicated formula.

(1+x)(x^4)/(1-x)^2=Kp.

Now, this makes no sense because I am not able to solve more than quadratics. This book should represent problems I could see on exams where they do not expect me to do more than quadratics. What do I do?

(b) DG=DGnaught+RTln(Q)
Q=Kp so DG=0.
DGnaught=28058J
DGnaught=DH-TDS.
DS=258mol/K.

(c) Reaction is endothermic. Adding temperature will make reaction go forward more.
 

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Part (a) does not look like it was set up correctly. If x is the final pressure of the NO2, the final pressure of the O2 is 1+x/4, and the final pressure of the final pressure of the N2O5 is 1-x/2. I guess you have to assume that the container is operating at constant volume.

Assume that x is small compared to 1, and see what you get. If you feel that you need to get better accuracy, solve by successive substitutions.

Chet
 
Chet, I corrected the situation:
I get a final x of 0.0147M. Please check my math.
(1+x)((4x)^4)/(1-2x)^2=Kp

Thank you so much.
 
Last edited:
I will post another problem on this thread. I do not want to overcrowd the forum with my "pollution."
 
Here is my attempt: calculate DGnaught using values (final - initial).
Calculate Kp noting that DG=0. So -DGnaught=RTln(Kp).
Use Clausius Clapeyron law to find new Kp at other temperature.

Kp 298K: 5.29x10^34
Kp 345K: 8.61x10^29
 

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yolo123 said:
Here is my attempt: calculate DGnaught using values (final - initial).
Calculate Kp noting that DG=0. So -DGnaught=RTln(Kp).
Use Clausius Clapeyron law to find new Kp at other temperature.

Kp 298K: 5.29x10^34
Kp 345K: 8.61x10^29
Your approach is correct. I haven't checked your arithmetic, or your use of units.

Chet
 

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