The general effect of an added electrolyte (i.e. an effect other than, or in addition
to, that due to its possible involvement as a reactant or
catalyst) on the observed
rate constant of a reaction in solution. At low concentrations (when only long-range coulombic
forces need to be considered) the effect on a given reaction is determined only by
the
ionic strength of the solution and not by the chemical identity of the ions. For practical purposes,
this concentration range is roughly the same as the region of validity of the
Debye–Hückel limiting law for activity coefficients. At higher concentrations, the effect
of an added electrolyte depends also on the chemical identity of the ions. Such specific
action can usually be interpreted as the incursion of a
reaction path involving an ion of the electrolyte as reactant or
catalyst, in which case the action is not properly to be regarded just as a kinetic electrolyte
effect. Kinetic electrolyte effects are usually (too restrictively and therefore incorrectly)
referred to as '
kinetic salt effects'. A kinetic electrolyte effect ascribable solely to the influence of the
ionic strength on activity coefficients of ionic reactants and transition states is called a '
primary kinetic electrolyte effect'. A kinetic electrolyte effect arising from the influence of the
ionic strength of the solution upon the
pre-equilibrium concentration of an ionic species that is involved in a subsequent
rate-limiting step of a reaction is called a '
secondary kinetic electrolyte effect'. A common case encountered in practice is the effect on the concentration of hydrogen
ion (acting as
catalyst) produced from the
ionization of a weak acid in a buffer solution. Synonymous with
kinetic equivalence.
Source:
PAC, 1994, 66, 1077
(Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994))
on page 1133