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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bekdemir, Yunus | - |
dc.contributor.author | Erturk, Aliye Gediz | - |
dc.contributor.author | Kutuk, Halil | - |
dc.date.accessioned | 2022-08-17T06:22:19Z | - |
dc.date.available | 2022-08-17T06:22:19Z | - |
dc.date.issued | 2014 | - |
dc.identifier.uri | http://doi.org/10.1002/poc.3242 | - |
dc.identifier.uri | http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2492 | - |
dc.description.abstract | The 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.iso | eng | en_US |
dc.publisher | WILEY111 RIVER ST, HOBOKEN 07030-5774, NJ | en_US |
dc.relation.isversionof | 10.1002/poc.3242 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | acid catalysis diarylsulfamides excess acidity hydrolysis mechanism | en_US |
dc.title | Investigation of the acid-catalyzed hydrolysis and reaction mechanisms of N,N '-diarylsulfamides using various criteria | en_US |
dc.type | article | en_US |
dc.relation.journal | JOURNAL OF PHYSICAL ORGANIC CHEMISTRY | en_US |
dc.contributor.department | Ordu Üniversitesi | en_US |
dc.contributor.authorID | 0000-0003-0831-7056 | en_US |
dc.identifier.volume | 27 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.startpage | 94 | en_US |
dc.identifier.endpage | 98 | en_US |
Appears in Collections: | Kimya |
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