2000
DOI: 10.3184/030823400103166814
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Kinetic Evidence of a Common Mechanism in the Oxidation by Chromium(vi) Complexes: Oxidation of Benzyl Alcohol

Abstract: The oxidation of benzyl alcohol by dichromate and seven chromium(VI) complexes in aqueous acetic acid in the presence of perchloric acid is first order each in the oxidants, the alcohol and the mineral acid. The oxidation conforms to the isokinetic and Exner relationships and follows a common mechanism.

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Cited by 3 publications
(2 citation statements)
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“…So are those dealing with the structure–reactivity relationships operating in these oxidations 8, 9. But reports on comparison of the rates and mechanisms of oxidations of a substrate by these reagents are a few; diphenyl sulfide in glacial acetic acid 10, diethyl sulfide 11, benzyl alcohol 12, 2‐propanol 13, and 1‐pentanol 14 in aqueous acetic acid individually exhibit identical kinetic behavior on oxidation with dichromates and halochromates of heterocyclic bases. Here, for the first time, we compare the reaction constants of the oxidations by dichromates, fluorochromates, chlorochromates, and bromochromate of heterocyclic bases; primary aliphatic alcohols have been chosen for the study, as the oxidation mechanism has been elucidated recently 14.…”
Section: Introductionmentioning
confidence: 99%
“…So are those dealing with the structure–reactivity relationships operating in these oxidations 8, 9. But reports on comparison of the rates and mechanisms of oxidations of a substrate by these reagents are a few; diphenyl sulfide in glacial acetic acid 10, diethyl sulfide 11, benzyl alcohol 12, 2‐propanol 13, and 1‐pentanol 14 in aqueous acetic acid individually exhibit identical kinetic behavior on oxidation with dichromates and halochromates of heterocyclic bases. Here, for the first time, we compare the reaction constants of the oxidations by dichromates, fluorochromates, chlorochromates, and bromochromate of heterocyclic bases; primary aliphatic alcohols have been chosen for the study, as the oxidation mechanism has been elucidated recently 14.…”
Section: Introductionmentioning
confidence: 99%
“…So are those dealing with the structure-reactivity relationships operating in these oxidations [8,9]. But reports on comparison of the rates and mechanisms of oxidations of a substrate by these reagents are a few; diphenyl sulfide in glacial acetic acid [10], diethyl sul- fide [11], benzyl alcohol [12], 2-propanol [13], and 1-pentanol [14] in aqueous acetic acid individually exhibit identical kinetic behavior on oxidation with dichromates and halochromates of heterocyclic bases. Here, for the first time, we compare the reaction constants of the oxidations by dichromates, fluorochromates, chlorochromates, and bromochromate of heterocyclic bases; primary aliphatic alcohols have been chosen for the study, as the oxidation mechanism has been elucidated recently [14].…”
Section: Introductionmentioning
confidence: 99%