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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 453-460 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of Ruthenium(III) chloride mediated oxidation of acetone, 2-butanone, 4-methyl-2-pentanone, 2-pentanone, cyclopentanone, and cyclohexanone by sodium periodate in aqueous HClO4 media was zero-order in [IO4-] and first-order in [ketone]. The reaction was independent of added [Ru(III)] and showed first-order dependence on [H+] for all the ketones studied, except acetone. In the case of acetone at [H+] 〈 0.05 M, the rate was independent of [H+], the order in [Ru(III)] being unity; but at [H+] 〉 0.05 M the reaction showed unit dependence on [H+] and the order in [Ru(III)] was zero. Ruthenium(VIII) generated in situ is postulated as the hydride abstracting species. A mechanism involving enolization as the rate determining step is proposed. Acetone at lower acidity of the medium is shown to react directly with Ru(VIII). In the absence of ruthenium(III) chloride, the kinetics were first-order in [IO4-], [ketone], and [H+]. Structure-reactivity relationship is discussed and thermodynamic parameters are reported. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 1267-1279 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of chlorination of toluene, o-methyl toluene, p-methyl toluene, m-methyl toluene, and m-chlorotoluene by chloramine-T(CAT) in aqueous acetic acid in the presence of HClO4 have been studied. The reaction is first order with respect to [CAT] as well as [H+]. The order with respect to the substrate is unity in the case of toluene and m-chlorotoluene, fractional in the case of o-methyl toluene and p-methyl toluene, and zero order in the case of m-methyl toluene. Nuclear halogenation has been observed with m-methyl toluene, while nuclear and side-chain halogenation for p-methyl toluene and o-methyl toluene, and sidechain halogenation for toluene and m-chlorotoluene are the pathways. An increase in the proportion of acetic acid accelerates the rate. Added acetate ions inhibit the reaction, and added p-toluene sulfonamide causes a pronounced retardation. A mechanism involving AcO+HCl as the important electrophile is discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 731-740 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of aldosugars and ketosugar by quinquevalent vanadium in binary mixtures of DMSO-water and acetic acid-water in sulfuric acid medium have been studied. The reaction is first order in both oxidant and substrate. The effect of acidity on the reaction kinetics has been determined. The effect of acidity shows a clear difference. The ketose has a unit dependence, whereas aldoses have a 0.5 dependence in H0. The role of solvent in these reactions has also been studied, and the effect of temperature on these reactions has been determined. A suitable mechanism has been postulated taking all the observed facts into consideration.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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