Investigation of the acid-catalyzed reactions of arylhydroxylamines

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dc.contributor.advisor Kruger, Terry L. en_US
dc.contributor.author Hartzell, Stephen L., 1944- en_US
dc.date.accessioned 2011-06-03T19:30:29Z
dc.date.available 2011-06-03T19:30:29Z
dc.date.created 1971 en_US
dc.date.issued 1971
dc.identifier LD2489.Z78 1971 .H37 en_US
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/handle/180201
dc.description.abstract AbstractEugen Bomberger's original work was concerned with the rearrangement of the substituted N-phenylhydroxylamines, but the mechanism responsible for the wide variety of products has remained unsettled.First, this investigation was concerned with a suitable synthesis for the substituted N-alkyl-N-phenylhydroxylamines. Secondly, a better understanding of the mechanism could be accomplished by the identification of the decomposition products and through a kinetic study of the rearrangement utilizing ultraviolet spectroscopy. The study was successful with the product identification of five decomposed substituted N-.phenylhydroxylamines, but numerous products, which interfered with the kinetic study, were isolated from the rearrangement and only uninterpretable kinetic data could be collected.Ball State UniversityMuncie, IN 47306 en_US
dc.format.extent v, 54 leaves : ill. ; 28 cm. en_US
dc.source Virtual Press en_US
dc.subject.lcsh Arylhydroxylamine. en_US
dc.subject.lcsh Hydroxylamine. en_US
dc.subject.other Ball State University. Thesis (M.S.) en_US
dc.title Investigation of the acid-catalyzed reactions of arylhydroxylamines en_US
dc.description.degree Thesis (M.S.)--Ball State University, 1971. en_US
dc.identifier.cardcat-url http://liblink.bsu.edu/catkey/416052 en_US


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  • Master's Theses [5256]
    Master's theses submitted to the Graduate School by Ball State University master's degree candidates in partial fulfillment of degree requirements.

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