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Study of initial state and transition state solvation in the Menschutkin reaction of triethylamine with ethyl iodide in alcohols from infinite dilution activity coefficients
Author(s) -
Gonçlalves Raquel M. C.,
Calado António R. T.,
Pinheiro Lídia M. V.,
Albuquerque Lídia M. P. C.,
Macedo Eugénia A.
Publication year - 1993
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/poc.610061011
Subject(s) - chemistry , triethylamine , unifac , activity coefficient , dilution , iodide , solvent , group contribution method , solvation , gibbs free energy , thermodynamics , ethyl iodide , organic chemistry , phase equilibrium , aqueous solution , phase (matter) , physics
The Gibbs energies of activation of the Menschutkin reactions of trethylamine with ethyl iodide in 10 monoalcohols and nine dialcohols, were dissected into contributions from the initial state and transition state. To perform this study, the infinite dilution activity coefficient values of the solutes in the solvents, γ ∞ , were determined by the UNIFAC group‐contribution method, using the modified Flory–Huggins equation in the combinatorial term. For triethylamine, the γ ∞ values were calculated using group‐interaction parameters from the VLE Parameter Table, due to the nonavailability of specific γ ∞ UNIFAC interaction parameters for the relevant groups. For ethyl iodide, the γ ∞ values were calculated using the group‐interaction parameters from the specific γ ∞ UNIFAC Parameter Table, except for the solvents diethylene glycol and triethlene glycol, where VLE parameters were used for the same reasons as explained above for the triethylamine. The results were compared with those obtained for the unimolecular decomposition of tert ‐butyl halides. For the Menschutkin reaction, we conclude that solvent disruption and reorganization to a state appropriate to solvating the molecular species is a dominant interaction mechanisim.