A Comparative investigation of the nucleophilic reactivities of hydroxide and phenoxide ions

dc.contributor.author	Jones, Richard Glyn
dc.date.accessioned	2010-11-22T23:19:46Z
dc.date.accessioned	2022-10-24T23:55:13Z
dc.date.available	2010-11-22T23:19:46Z
dc.date.available	2022-10-24T23:55:13Z
dc.date.copyright	1961
dc.date.issued	1961
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/22605
dc.description.abstract	In considering the rates of bimolecular nucleophilic substitution and elimination reactions, it has been a common practice to draw analogies between the nucleophilic character of the reagent and its basicity. If basicity can be considered to be a measure of nucleophilicity then the sequences OH-, OPh-, OAc-, Cl- or OR-, SR-, SeR- should correspond to a decreasing nucleophilic strength, just as they do to a decreasing basic strength. Since, however, the basicity of a reagent is its nucleophilic affinity for hydrogen ions	en_NZ
dc.format	pdf	en_NZ
dc.language	en_NZ
dc.language.iso	en_NZ
dc.publisher	Te Herenga Waka—Victoria University of Wellington	en_NZ
dc.title	A Comparative investigation of the nucleophilic reactivities of hydroxide and phenoxide ions	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ

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