Association in solution includes replacement of solute–solvent contacts, not just formation of the isolated dimer. cyclohexane solvates the benzene surface well through dispersion. Much of the London dispersion gained on bringing two benzene molecules together replaces comparable benzene–cyclohexane contacts, leaving only a modest net gain before the translational and orientational entropy penalty. cyclohexane cannot provide the complementary donor/acceptor interactions available when two waters hydrogen-bond, so water association gains a more distinctive interaction relative to its separated solvated monomers.
Using the same concentration standard state, and . For illustration at 298 K and , the ratio of the two supplied association constants corresponds to
Thus the water-molecule pair can associate more favourably in this solvent even though the stipulated isolated-pair binding energies are similar. Gas-phase potential energy alone omits both differential solvation and the entropy of association.

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