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A friend tells you “Free energy G and pressure P are directly related by the equation

G=G°+RTln(P)

Also, G is related to the equilibrium constant K in that when Gproducts = Greactants, the system is at equilibrium. Therefore, it must be true that a system is at equilibrium when all pressures are equal.” Do you agree with this friend? Explain.

Short Answer

Expert verified

No, I wouldn’t agree because at equilibrium, free energy change is zero not the value of free energy.

Step by step solution

01

Relationship between Gibbs Free Energy change and Equilibrium Constant   

At Equilibrium change in Gibbs free energy is zero, i.e,

ΔG=Gproducts-Greactants=0

So that

ΔG=ΔG°-RTlnK=0ΔG°=RTlnK

02

Equilibrium and Pressure

So we can say from the equation that free energy change is zero at equilibrium not the value of free energy so we cannot say that for equilibrium pressure of all part must be equal.

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Most popular questions from this chapter

Consider the reaction

Fe2O3(s)+3H22Fe(s)+3H2O(g)

  1. Use ΔGrovalues in appendix 4 to calculate ΔGofor third reaction.
  2. Is this reaction spontaneous under standard conditions at 298K.
  3. The value of ΔHofor this reaction is 100KJ. At what temperatures is this reaction spontaneous at standard conditions? Assume that ΔHo and ΔSodo not depend on temperature.

How can one estimate the value of K at temperatures other than 25°C for a reaction? How can one estimate the temperature where K = 1 for a reaction? Do all reactions have a specific temperature where K = 1?

Consider 1.00 mole of an ideal gas at 25°C.
a. Calculate q,w,E,S,HandG for the expansion of this gas isothermally and irreversibly from 2.45×10-2 atm to 2.45×10-3 atm in one step.
b. Calculate for the same change of pressure as in part a but performed isothermally and reversibly.
c. Calculate localid="1649303003894" q,w,E,S,HandGfor the one-step so thermal, irreversible compression of 1.00 mole of an ideal gas at 25°C from 2.45×10-3atm to 2.45×10-3atm.
d. Construct the PV diagrams for the processes described in parts a, b, and c.
e. Calculate the entropy change in the surroundings for the processes described in parts a, b, and c.

The enthalpy of vaporization of chloroform (CHCI3) is 31.4KJ/moleat its boiling point (61.7°C).DetermineΔSsys,ΔSsurr,andΔSuniv when 1.00 mole of chloroform isvaporized at 61.7°C and 1.00 atm.

Consider 1.00 mole of an ideal gas that is expanded isothermally at 25°C from 2.45 ×10-2 atm to 2.45 ×10-3 atm in the following three irreversible steps:

Step 1: from 2.45 ×10-2atm to 9.87 ×10-3 atm
Step 2: from 9.87 × 10-3 atm to 4.97 ×10-3 atm

Step 3: from 4.97 ×10-3atm to 2.45 ×10-3 atm

Calculate q,w,E,S,HandGfor each step andfor the overall process.

See all solutions

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