In a considerable number of cases plots of T ![[Delta]](/img3/D_files/DDELTA.gif)
S vs. ![[Delta]](/img3/D_files/DDELTA.gif)
H, for a series of reactions, e.g. for a reaction in a range of different solvents, are straight lines of approximately unit slope. Therefore, the terms ![[Delta]](/img3/D_files/DDELTA.gif)
H and T ![[Delta]](/img3/D_files/DDELTA.gif)
S in the expression partially compensate, and ![[Delta]](/img3/D_files/DDELTA.gif)
G = ![[Delta]](/img3/D_files/DDELTA.gif)
H - T ![[Delta]](/img3/D_files/DDELTA.gif)
S often is a much simpler function of solvent (or other) variation than ![[Delta]](/img3/D_files/DDELTA.gif)
H or T ![[Delta]](/img3/D_files/DDELTA.gif)
S separately. CONNOR (1991). See also isokinetic relationship.
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