The existence of a high-density phase separation for molecular and con
tinuum solvent models of ion-water solutions are demonstrated using th
e DRISM/HNC theory. The molecular lever effects which influence solubi
lity and the inability of continuum models to exhibit some of these ef
fects are discussed. The general trends in experimental alkali halide
solubilities are found to be consistent with the present model calcula
tions. The dependence of the phase separation on ion size is found to
be primarily entropic in nature.