Please use this identifier to cite or link to this item: http://13.232.72.61:8080/jspui/handle/123456789/2233
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dc.contributor.authorRamachandrappa, R.-
dc.contributor.authorIyengar, Pushpa-
dc.contributor.authorJoseph, Usha-
dc.date.accessioned2019-05-17T10:20:34Z-
dc.date.available2019-05-17T10:20:34Z-
dc.date.issued2012-10-
dc.identifier.citationRamachandrappa, R., Iyengar, Pushpa., Joseph, Usha. (2013). Kinetics and Mechanistic Studies on Oxidation of Levocarnitine by Bromamine-T in HCl Medium Catalyzed by Ru (III). Journal of Chemistry, 2013, 1-7.en_US
dc.identifier.urihttp://dx.doi.org/10.1155/2013/574626-
dc.identifier.urihttp://13.232.72.61:8080/jspui/handle/123456789/2233-
dc.description.abstractA kinetic study on RuCl3-catalysed oxidation of levocarnitine (LC) by sodium N-bromo-p-toluenesulphonamide or bromamine-T (BAT) has been carried out in HCl medium at 303 K. The reaction rate shows a 􀄕rst order dependence on [BAT]0 and fractional order with respect to both [LC]0 and [H+]. Addition of the reaction product, p-toluenesulphonamide, retards the rate. e addition of RuCl3 and chloride ions to the reaction mixture shows an increase in the rate of the reaction. e dielectric effect is positive. e variation of ionic strength of the medium has no signi􀄕cant effect on the rate of the reaction. e reaction fails to initiate polymerization of acrylamide. Michaelis-Menten type of kinetics has been proposed. ermodynamic parameters have been computed from Arrhenius plot by studying the reaction at different temperatures.The reaction stoichiometry and oxidation products were identi􀄕ed. Based on the experimental observations a suitable mechanism was proposed and rate law deduced.en_US
dc.language.isoenen_US
dc.publisherHindawi Publishing Corporationen_US
dc.subjectChemistryen_US
dc.subjectOxidationen_US
dc.subjectLevocarnitineen_US
dc.titleKinetics and Mechanistic Studies on Oxidation of Levocarnitine by Bromamine-T in HCl Medium Catalyzed by Ru(III)en_US
dc.typeArticleen_US
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