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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/31664
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dc.contributor.advisorWarkentin, J.-
dc.contributor.authorTee, Oswald Sydney-
dc.date.accessioned2025-05-11T21:34:58Z-
dc.date.available2025-05-11T21:34:58Z-
dc.date.issued1965-09-
dc.identifier.urihttp://hdl.handle.net/11375/31664-
dc.description.abstractThe relative rates of hydrogen deuterium exchange at the α- and α' -positions in the simplest unsymmetrical ketone were determined by use of N.M.R. spectroscopy. It has been long held that in base-catalysed enolization processes the least alkyl substituted opposition is cost reactive. However it was observed that in the exchange reaction of 2-butanone catalyzed by OD- in D2O, the α- and α'-positions are similarly reactive while for weaker bases (p-NO2PHO-, AcO- ) the cost substituted α- position is the more reactive. The results are discussed in terms of a model for the transition state for enolization, and a continuity of mechanism between the acid-catalyzed, and base-catalyzed processes is proposed.en_US
dc.language.isoenen_US
dc.subjectRelative ratesen_US
dc.subjectHydrogenen_US
dc.subjectDeuteriumen_US
dc.subjectMethyl Ethyl Ketoneen_US
dc.subjectEnolizationen_US
dc.subjectN.M.R. spectroscopyen_US
dc.titleTHE RELATIVE RATES OF BΛSE-CATALYSED HYDROGEN-DEUTERIUM EXCHANGE IN METHYL ETHYL KETONEen_US
dc.title.alternativeBASE-CATALYZED HYDROGEN-DEUTERIUM EXCHANGE OF A SIMPLE KETONEen_US
dc.typeThesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreetypeThesisen_US
dc.description.degreeMaster of Science (MSc)en_US
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