Many individuals have been perplexed by the seeming incompatibility in the different temperature dependencies of the equilibrium constant K for a chemical reaction and the degree of spontaneity of the same reaction as measured by the standard Gibbs function difference DG°. A related apparent inconsistency is that the temperature of a maximum or minimum in K does not correspond to the temperature of an extremum in DG° for the same reaction. These paradoxes vanish if we use the Planck function instead of the Gibbs function as our criterion of spontaneity. Furthermore, the Planck function provides a more direct connection to the combined first and second laws of thermodynamics.
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Citation
Rosenberg, Robert M.; Klotz, Irving M. J. Chem. Educ.1999 76 1448.
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