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 |