In concentrated chloride media, nickel is reduced at far more positive potentials than in dilute solutions. The positive shift in half-wave potential increases as the ionic strength is raised, and is also greater when the cation of the supporting electrolyte has a high hydration number. Evidence is presented to show that the reduction in overpotential is due to the formation of a nickel chloride complex, [Ni(H2O)5Cl]+, which has a stoicheiometric stability constant of 0.094 � 0.009 at an ionic strength of 10.0. Spectrophotometric results show that this nickel species is not formed in low ionic strength solutions. In anhydrous methanol saturated with lithium chloride, nickel is present as the tetrachloro complex, [NiCl,]2-, which has similar polarographic behaviour to the monochloro complex. Current-potential curves recorded at a rotated pyrolytic graphite electrode enabled the behaviour of nickel to be studied in the absence of specific adsorption of the chloride ion. Nickel is reduced at more positive potentials at a dropping mercury electrode than at the pyrolytic graphite electrode, and the results indicate that this difference is due to specific adsorption of chloride on the mercury electrode.