Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16090
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dc.contributor.authorReddy, Ch Sanjeeva-
dc.contributor.authorKumar, T Vijaya-
dc.date.accessioned2013-02-26T19:30:29Z-
dc.date.available2013-02-26T19:30:29Z-
dc.date.issued1999-11-
dc.identifier.urihttp://hdl.handle.net/123456789/16090-
dc.description1188-1194en_US
dc.description.abstractUncatalysed acid bromate oxidation of lactic acid (LA) exhibits fractional order (1.6) in [acid) and first order each in [Br(V)) and [LA]. Kinetic isotope effect (kH/kD=1) is absent, however an in verse solvent isotope effect (kH2O /  kD2O = 1.78 at 313 K) is observed. The mechanism proposed consists of a rate determining formation of bromate ester due to the nucleophilic attack by the alcoholic / hydroxyl group at the bromine atom of HOBrO2/ H2O22Br+O, followed by a fast disproportionation of the ester through C-C bond cleavage to form products. Oxovanadium(lV)-catalysed LA-Br(V) reaction exhibits second order in [acid], fraction al order in [lactic acid) and first order each in [VOSO4] and [oxidant]. The envisaged mechanism assumes a ternary complex formation involving a binary complex of LA and V(IV) and protonated bromate, which subsequently decomposes to the intermediate/products. The rate constants involved for each step of thc react ions are evaluated along with their thermodynamic parameters.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.38A(11) [November 1999]en_US
dc.titleMechanism of oxovanadium (IV)catalysed and uncatalysed bromate oxidation of lactic acid in acid medium: Evaluation of composite and individual kinetic and thermodynamic parametersen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.38A(11) [November 1999]

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