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Strong hydrogen bonding in organic synthesis

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dc.contributor.author So, Kwok-Hung. en_US
dc.date.accessioned 2009-07-09T18:43:03Z
dc.date.available 2009-07-09T18:43:03Z
dc.date.issued 1978-07-09T18:43:03Z
dc.identifier.uri http://hdl.handle.net/10464/2072
dc.description.abstract The preparation of phenacyl and para-phenylphenacyl esters, the reactions of carboxylic acids, phenols, 2-nitropropane and alcohols with alkyl halides in the presence of fluoride anion are described. The reactions are thought to be accelerated by the formation of hydrogen bonds between the fluoride anion and the organic electron acceptor. The fluoride ,carboxylic acids, fluoride-phenols and fluoride-2-nitropropane are better reaction systems than the fluoride-alcohol. The source of the fluoride anion and the choice of solvents are also discussed. en_US
dc.language.iso eng en_US
dc.publisher Brock University en_US
dc.subject Organic compounds--Synthesis. en_US
dc.subject Hydrogen bonding. en_US
dc.title Strong hydrogen bonding in organic synthesis en_US
dc.type Electronic Thesis or Dissertation en_US
dc.degree.name M.Sc. Chemistry en_US
dc.degree.level Masters en_US
dc.contributor.department Department of Chemistry en_US
dc.degree.discipline Faculty of Mathematics and Science en_US


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