Thermodynamics equilibrium constant problem

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SUMMARY

The discussion focuses on calculating the equilibrium constant (Keq) for the reaction N2 + 3H2 --> 2NH3 at 500K and estimating the percentage conversion at equilibrium under different pressures (1 bar and 50 bar). The Van Hoff equation is utilized to determine Keq, while Dalton's law of partial pressures is applied to find initial partial pressures of reactants. The participants clarify that the initial partial pressures for N2 and H2 are 1/4 bar and 3/4 bar, respectively, leading to the establishment of an ICE table for further calculations. Ultimately, the user successfully resolves the problem with guidance from peers.

PREREQUISITES
  • Understanding of the Van Hoff equation for equilibrium constants
  • Knowledge of Dalton's law of partial pressures
  • Familiarity with ICE tables for equilibrium calculations
  • Basic concepts of gas stoichiometry
NEXT STEPS
  • Study the application of the Van Hoff equation in different temperature scenarios
  • Learn how to construct and interpret ICE tables for various chemical reactions
  • Explore the implications of pressure changes on equilibrium positions
  • Investigate the effects of temperature on equilibrium constants
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Chemistry students, educators, and professionals involved in chemical equilibrium analysis and thermodynamics, particularly those focusing on gas-phase reactions.

Samuel1321
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Homework Statement



N2 + 3H2 --> 2NH3 (all gases)

Why is such a high pressure needed? Calculate the equilibrium constant at 500k then estimate the percentage conversion at equilibrium at 1 bar total pressure, assuming the stoichiometric ratio of N2:H2 is 1:3.

Repeat the process at 50 bar.

Homework Equations



Van Hoff equation : ln(keq) at final temp = -((delta G)/RTi) - ((delta H)/R)(1/Tf-1/Ti)

Keq = ((PNH3)^2)/((PH2)^3)(PN2)

PNH3 + PH2 + PN2 = 1 bar

The Attempt at a Solution


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I solved for keq at 500k. I have no idea how to estimate the percentage conversion at equilibrium at 1 bar total pressure since we aren't given any of the partial pressures.

I tried using molar ratios to solve but it doesn't really make sense. Here's what I did 1x + 3x + 2x = 1, 6x=1 x=0.33 = 33%. For 50 bar 1x+3x+2x=50, then 6x=50, x would be over 100%.
 
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What are the initial partial pressures at 1 bar? What are the initial partial pressures at 50 bars?
 
Chestermiller said:
What are the initial partial pressures at 1 bar? What are the initial partial pressures at 50 bars?

They did not say what the initial pressures are.
 
Samuel1321 said:
They did not say what the initial pressures are.
You know the total pressure and the mole fractions of H2 and N2. So, from Dalton's law of partial pressures, what are the initial partial pressures of H2 and N2?
 
Chestermiller said:
You know the total pressure and the mole fractions of H2 and N2. So, from Dalton's law of partial pressures, what are the initial partial pressures of H2 and N2?

So assuming that there is no product in at the beginning of the reaction, partial pressure of N2 would be 1/3 bar and the partial pressure of H2 would be 2/3 bar.
 
Samuel1321 said:
So assuming that there is no product in at the beginning of the reaction, partial pressure of N2 would be 1/3 bar and the partial pressure of H2 would be 2/3 bar.
No, 1/4 and 3/4. These are the mole fractions.
 
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Chestermiller said:
No, 1/4 and 3/4. These are the mole fractions.

Oh right, just had a brain fart, don't know how I missed that. So how should I proceed? Should I set up an equation for Keq?
 
Let x be the fraction of the reactants converted to ammonia. What are the new mole fractions of N2 and H2, and what is the mole fraction ammonia.
 
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Chestermiller said:
Let x be the fraction of the reactants converted to ammonia. What are the new mole fractions of N2 and H2, and what is the mole fraction ammonia.
Thanks for the reply! I appreciate the help! I asked my professor and I figured it out.
 

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