Gibbs Free energy vs Gibbs Free energy at standard state

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SUMMARY

ΔG° represents the Gibbs Free energy change at 1 bar, while ΔG is a general term that does not adhere to the same conditions. In equilibrium reactions, ΔG equals zero, indicating a specific ratio of reactants to products, which is not 100% reactants or products. The relationship between ΔG°, ΔH°, and ΔS° is crucial for determining the temperature at which equilibrium occurs, using the equation ΔG° = ΔH° - TΔS°. The confusion arises from the interpretation of ΔG° as a non-zero value in certain contexts, particularly in phase changes.

PREREQUISITES
  • Understanding of Gibbs Free energy concepts
  • Familiarity with thermodynamic equations, specifically ΔG°, ΔH°, and ΔS°
  • Knowledge of equilibrium reactions and their characteristics
  • Basic grasp of phase changes in thermodynamics
NEXT STEPS
  • Study the derivation and applications of the Gibbs Free energy equation
  • Learn about the implications of ΔG° in various chemical reactions
  • Investigate the relationship between ΔH° and ΔS° in phase transitions
  • Explore graphical representations of reversible reactions and their equilibria
USEFUL FOR

Chemistry students, researchers in thermodynamics, and professionals involved in chemical engineering or physical chemistry will benefit from this discussion.

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ΔG° is the measure of Gibbs Free energy change at 1 bar but no specified temperature and also the stoichiometric amounts depending on the equation of the chemical reaction.

For example, if X ->2Y then the ΔG° would be equal to ΔG°f(2Y)-ΔG°f(X). While for ΔG it is a general term for Gibbs Free Energy that might not have the same properties as the ΔG° (1 bar, stoichiometric amounts)

So I was wondering, for a equilibrium reaction the ΔG=0 as when it reaches the lowest point the gradient=0. At this point, there is a certain composition of reactants to products that would not be 0% reactants and 100% products as that would mean the reaction is irreversible and reaches a lowest point at 100% products.

The graph for the reversible reaction would look like this: http://postimg.org/image/r9vtp0fh3/

So now in most questions, such as in phase changes questions they would give us the ΔH° and ΔS° and they then would want us to find the temperature at which equilibrium takes place. So using the formula ΔG°=ΔH°-TΔS° we would let ΔG° be 0 and solve for T. The part that i don't get is that ΔG° is a non-zero value and that we shouldn't be able to use ΔH° or ΔS° to find ΔG because either ΔH° or ΔS° represents 100% complete reaction. So I'm not sure why we are allowed to do those thing actually.

Thanks in advance for the help :)
 
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For the case of a. phase change, the ##\Delta\ zeros## are not at 1 bar. So their definitions are totally different.
 

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