Solvent polarity and organic reactivity in mixed solvents: evidence using a reactive molecular probe to assess the role of preferential solvation in aqueous alcohols

J Org Chem. 2005 Mar 4;70(5):1647-53. doi: 10.1021/jo048163j.

Abstract

Product selectivities [S = ([ester product]/[acid product]) x ([water]/[alcohol solvent])] are reported for solvolyses of p-methoxybenzoyl chloride (2) in aqueous methanol, ethanol, 2,2,2-trifluoroethanol, n-propyl alcohol, isopropyl alcohol, and tert-butyl alcohol at 25, 35, and 45 degrees C. S values are small and depend significantly on the alcohol cosolvent, varying from 1.3 in methanol to 0.1 in tert-butyl alcohol, but S depends only slightly on the solvent composition, and on the temperature. As S adjusts the product ratios for changes in bulk solvent compositions, it is suggested that preferential solvation by either alcohol or water at the reaction site is not a major factor influencing rates or products. Logarithms of rates of solvolyses of 2 correlate well with Kosower Z values (based on solvatochromism). In contrast, another solvatochromic polarity index, E(T)(30), shows "dispersion" in correlations with the solvent ionizing power parameter, Y(OTs), probably due to aromatic ring and other solvation effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemistry*
  • Benzoates / chemistry*
  • Hydrolysis
  • Molecular Probes / chemistry*
  • Molecular Structure
  • Solvents / chemistry*
  • Water / chemistry

Substances

  • Alcohols
  • Benzoates
  • Molecular Probes
  • Solvents
  • Water
  • benzoyl chloride