Gibbs Free energy vs Gibbs Free energy at standard state

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ΔG° measures the change in Gibbs Free Energy at 1 bar and specific stoichiometric amounts for a chemical reaction, while ΔG is a more general term that may not adhere to these conditions. At equilibrium, ΔG equals zero, indicating a balance between reactants and products, which does not imply complete conversion to products. The discussion highlights confusion regarding the use of ΔH° and ΔS° to determine temperature at equilibrium, particularly when ΔG° is considered non-zero. It is noted that phase change scenarios involve different definitions of ΔG° that may not apply at 1 bar. Understanding these distinctions is crucial for accurately applying thermodynamic principles in chemical reactions.
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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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