Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46809
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dc.contributor.authorSharma, L R-
dc.contributor.authorSingh, Gurcharan-
dc.contributor.authorSharma, Arun-
dc.date.accessioned2019-03-26T11:10:43Z-
dc.date.available2019-03-26T11:10:43Z-
dc.date.issued1989-09-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46809-
dc.description757-759en_US
dc.description.abstractCyclcic voltammetry (anodic) of o-chlorophenol has been carried out in six background solutions having different acidities. The first forward scan exhibits a single oxidation peak in each case. During the subsequent cyclic operation, three additional redox couples appear in sulphuric acid solutions of concentrations 1.0 M and 0.1 M, two redox couples appear in buffer of pH 4.5 and one redox couple appears in buffers of pH 6.0 and 8.5. A plausible explanation for this typical redox behaviour which is considerably different from that of phenol and o-cresol has been offered on the basis of free radical couplings followed by acid-favoured intramolecular rearrangements in the reaction intermediates.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.28A(09) [September 1989]en_US
dc.titleRedox behaviour of o-chlorophenol in aqueous solutionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(09) [September 1989]

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