Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols

Curry, Omadee

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dc.contributor.author	Curry, Omadee	en_US
dc.date.accessioned	2013-10-21T14:48:21Z
dc.date.accessioned	2019-09-08T02:48:32Z
dc.date.available	2013-10-21T14:48:21Z
dc.date.available	2019-09-08T02:48:32Z
dc.date.issued	2013
dc.identifier	864303524	en_US
dc.identifier.other	b21400350	en_US
dc.identifier.uri	http://hdl.handle.net/1989/10452
dc.description	viii, 73 leaves : illustrations ; 29 cm.	en_US
dc.description.abstract	This thesis utilizes the method of One Pot synthesis to synthesize a series of alkyl functional groups. These group include...an alkyl azide, alkyl esters, and an alkyl chloride. Results showed that both primary and secondary alcohols were converted into products within the previously mentioned functional groups. The steric environment of each alcohol reagent dictated which product was produced. All of the findings... within this research were supported by high yields, appropriate spectrum data, and confirmed to be consistent with finding within previous literature.	en_US
dc.description.statementofresponsibility	by Omadee Curry.	en_US
dc.language.iso	en_US	en_US
dc.relation.ispartofseries	Master's Theses no. 1411	en_US
dc.subject.lcsh	Functional groups.	en_US
dc.subject.lcsh	Chemistry, Organic.	en_US
dc.title	Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols	en_US
dc.type	Thesis	en_US

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