Oxidation of benzyl alcohol by pyridinium dichromate in acetonitrile. Using the para/meta ratio of substituent effects for mechanism elucidationElectronic supplementary information (ESI) available: Table S1 containing kinetic data for establishing rate laws. See http://www.rsc.org/suppdata/p2/b2/b200742h/

Abstract

Rate constants were measured for the oxidation reaction of benzyl alcohol and twenty-five ortho-, meta- and para-monosubstituted derivatives in the temperature range 293–323 K at intervals of 10 K. The kinetics were followed spectrophotometrically in dry acetonitrile acidified with trichloroacetic acid (TCA) using pyridinium dichromate (PDC) as oxidising agent under pseudo-first-order conditions with respect to PDC. Benzaldehyde is the only oxidation product and no reaction takes place without TCA. From good linear Eyring plots activation enthalpies Δ‡H° and entropies Δ‡S° are calculated. For ortho-substituted benzyl alcohols high Δ‡H° values and small negative Δ‡S° values point to an ortho effect on the rate-determining step. Using the tetralinear approach to substituent effects, the average value = 1.09 ± 0.05 for the para/meta ratio of inductive or Electra effects is obtained and negative Hammett reaction constants decreasing in magnitude with increasing temperature are found. A mechanism implicating the prior acid-catalysed formation of neutral benzyl hydrogen dichromate ester followed by intramolecular proton transfer is proposed. Modelling of parameter λ in terms of the electrostatic theory showed its experimental value to be consistent with the ratio of electric potentials generated in the immediate vicinity of the nearest chromium atom by dipolar substituents introduced in the aromatic ring on para and meta positions. At a molecular level the oxidative, rate-determining step is suggested to be triggered by the retraction or shrinkage of electron pairs from sigma bonds in Cr2VI species to non-bonding orbitals in unstable CrIV–O–CrVI species. In contrast with past interpretations, an electrochemical approach is used to explain negative values for the Hammett reaction constant.