Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2492
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dc.contributor.authorBekdemir, Yunus-
dc.contributor.authorErturk, Aliye Gediz-
dc.contributor.authorKutuk, Halil-
dc.date.accessioned2022-08-17T06:22:19Z-
dc.date.available2022-08-17T06:22:19Z-
dc.date.issued2014-
dc.identifier.urihttp://doi.org/10.1002/poc.3242-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2492-
dc.description.abstractThe mechanism of acidaEurocatalyzed hydrolysis of a series of paEurosubstituted N,NaEuro(2)aEurodiarylsulfamides was investigated in aqueous mineral acid solutions. Rate profiles, reaction activation parameters, catalytic order of strong acids, solvent isotope effects, and analysis of the kinetic data by the excess acidity method suggest a change in the mechanism from A2 to A1. While the hydrolysis proceeds with an A2 mechanism in low acidity regions, an A1 mechanism takes place in high acid concentrations. Copyright a (c) 2013 John Wiley & Sons, Ltd.en_US
dc.language.isoengen_US
dc.publisherWILEY111 RIVER ST, HOBOKEN 07030-5774, NJen_US
dc.relation.isversionof10.1002/poc.3242en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectacid catalysis diarylsulfamides excess acidity hydrolysis mechanismen_US
dc.titleInvestigation of the acid-catalyzed hydrolysis and reaction mechanisms of N,N '-diarylsulfamides using various criteriaen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF PHYSICAL ORGANIC CHEMISTRYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0003-0831-7056en_US
dc.identifier.volume27en_US
dc.identifier.issue2en_US
dc.identifier.startpage94en_US
dc.identifier.endpage98en_US
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