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Strong hydrogen bonding in organic synthesis

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Show simple item record So, Kwok-Hung. en_US 2009-07-09T18:43:03Z 2009-07-09T18:43:03Z 1978-07-09T18:43:03Z
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 M.Sc. Chemistry en_US Masters en_US
dc.contributor.department Department of Chemistry en_US Faculty of Mathematics and Science en_US

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