Please use this identifier to cite or link to this item: http://repository.aaup.edu/jspui/handle/123456789/1371
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dc.contributor.authorAmer, Iqab$AAUP$Palestinian-
dc.date.accessioned2021-05-10T08:08:57Z-
dc.date.available2021-05-10T08:08:57Z-
dc.date.issued2021-
dc.identifier.issnDOI: 10.21608/EJCHEM.2020.22459.2338-
dc.identifier.urihttp://repository.aaup.edu/jspui/handle/123456789/1371-
dc.description.abstractThe reaction of 2-methylindole with hexacyanoferrate(III) in alkaline media to produce the corresponding 2-methylindolin-3-one has been studied at constant temperature and ionic strength. The reaction followed first order kinetics with respect to [2-methylindole], [OH-] and [Fe(CN)63-]. The effects of added electrolytes, potassium hexacyanoferrate(II), relative permitivity and temperature have also been studied. On the basis of experimental observations, a probable reaction mechanism has been proposed.en_US
dc.language.isoenen_US
dc.publisherNational Information and Documentation Centre(NIDOC)en_US
dc.relation.ispartofseriesEgypt. J. Chem. Vol. 64;No. 3 pp. 1441-1446 (2021)-
dc.titleKinetics and Mechanism of The Oxidation of 2-Methylindole by Alkaline Potassium Hexacyanoferrate(III)en_US
dc.typeArticleen_US
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