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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/20681
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DC FieldValueLanguage
dc.contributor.advisorWarkentin, J.-
dc.contributor.authorWest, Paul Ronald-
dc.date.accessioned2016-10-14T12:41:36Z-
dc.date.available2016-10-14T12:41:36Z-
dc.date.issued1967-03-
dc.identifier.urihttp://hdl.handle.net/11375/20681-
dc.description.abstract<p> The reaction of lead tetra-acetate with ketone carbohydrazones and 4-substituted semicarbazones gave a series of 2-(substituted imino)-△^3-1,3,4-oxadiazolines. Spectroscopic and chemical evidence is presented to establish the proposed structure, and the scope of the reaction is described. The thermolysis of the 5,5-diaryl-2-phenylimino-△^3-1,3,4-oxadiazolines was studied in chlorobenzene solution. The results of kinetic experiments (gas evolution and infra-red) are reported, and the mechanism of the decomposition is discussed. A survey of the literature pertaining to related lead tetra-acetate oxidations, and to decomposition of cyclic azo compounds is presented.</p>en_US
dc.language.isoen_USen_US
dc.subjectoxidative, cyclization, ketone, carbohydrazones, semicarbazones, decomposition, reactionen_US
dc.titleThe Oxidative Cyclization of Ketone Carbohydrazones and 4-Substituted Semicarbazones. Thermal Decomposition of 5,5-Diaryl-2-Phenylimino-△^3 -1,3,4-Oxadiazolinesen_US
dc.typeThesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreetypeThesisen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
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