The nature of a critical complex may often be related to the change of the rate of the corresponding reaction when the solvent medium is varied by altering either the electrolyte concentration or the dielectric constant. It is necessary to take into consideration the ratio of volume concentration to mole fraction, the possibility of catalytic action, even that due to an ionic charge, and the possibility that the nature of the critical complex may change with changing composition. The critical complex of the bromoacetate‐thiosulfate reaction appears to be the two tangent ions. In the ammonium‐cyanate reaction there may be a partial de‐polarization of the tangent ions. The effect of changing dielectric constant on the solvolysis of tertiary butyl chloride indicates a rather wide separation of the ions in the critical complex.

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This paper has been written after the Conference of the Section of Physics and Chemistry of the New York Academy of Sciences on February 24, 1939, at which papers in this field were presented by (a) Eyring and Laidler, (b) J. C. Warner, and (c) P. D. Bartlett; and after the presentation at the Baltimore meeting of the American Chemical Society of the paper by (d) Laidler and Eyring. Although many of the ideas were developed before these meetings and were put forward at the Conference, others arose from these papers and their discussion. The author has attempted to give proper credit, but it must be remembered that citations refer to a memory, which may not be accurate, of an oral report which may differ from the written paper.
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This theory differs from that of La Mer and Kamner, references 7 and 9, only in recognizing that the complex ions do not greatly outnumber the simple ions in the range of experimental measurements, and that their effect must vanish at zero concentration.
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The activity coefficients of ions as determined by the solubilities of electrolytes behave qualitatively in the same manner.
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