How to Find Equilibrium Pressures for NO₂ and N₂O₄ at 298 K?

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SUMMARY

The discussion focuses on calculating the equilibrium pressures of nitrogen dioxide (NO₂) and dinitrogen tetroxide (N₂O₄) at 298 K for the reaction 2 NO₂(g) ↔ N₂O₄(g). The standard enthalpy change (ΔH°_{rxn}) is -57.2 kJ, and the standard entropy change (ΔS°_{rxn}) is -175.8 J/K. The equilibrium constant (K_{eq}) was calculated to be 6.973 using the relation ΔG°_{rxn} = -RTln(K_{eq}). For constant pressure conditions, the equilibrium constant is determined to be 1, indicating that ΔG_{rxn} approaches zero.

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  • Understanding of thermodynamic equations, specifically dG = VdP - SdT
  • Knowledge of equilibrium constants and their relation to free energy
  • Familiarity with standard enthalpy and entropy changes
  • Basic principles of gas behavior under varying pressure and volume conditions
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  • Study the derivation of the Gibbs free energy equation in thermodynamics
  • Learn how to calculate equilibrium constants from free energy changes
  • Explore the effects of temperature and pressure on chemical equilibria
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Homework Statement



For the reaction

2 NO_{2}(g) \leftrightarrow N_{2}O_{4}(g)

ΔH°_{rxn} = -57.2 kJ and ΔS°_{rxn} = -175.8 J/K

A 1 L container is initially filled with 1 atm of NO_{2} at 298 K. Find the equilibrium pressures of NO_{2} and N_{2}O_{4} at 298 K if

a. volume is held constant

b. pressure is held constant

Homework Equations



dG = VdP - SdT

The Attempt at a Solution



So using the fundamental thermodynamic equation above, I found that ΔG = -4811.6 J. SdT goes to zero since the temperature doesn't appear to change. VdP can be substituted withdH -TdS, with all three values available in the problem.

So using the following relation between K_{eq} and free energy:

ΔG°_{rxn} = -RTln(K_{eq})

Solving for K_{eq}, I obtain 6.973

So from this point, how do I calculate the partial pressures of NO_{2} and N_{2}O_{4}? Can I stop at 6.973?

As for the second question, I find that if pressure is held constant, the equilibrium constant is just 1, since ΔG_{rxn} goes to zero.
 
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How is the equilibrium constant expressed in terms of the partial pressures of NO2 and N2O4? Also note that the standard heat of reaction and standard entropy change of reaction are evaluated at constant pressure (1 atm), not constant volume. So the problem you have been working on is really problem 2. You have yet to address problem 1.
 

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