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Halogen addition to acetylenic compounds

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dc.contributor.author Dasent, W. E.
dc.date.accessioned 2011-12-13T21:18:17Z
dc.date.accessioned 2022-10-31T21:12:56Z
dc.date.available 2011-12-13T21:18:17Z
dc.date.available 2022-10-31T21:12:56Z
dc.date.copyright
dc.date.copyright 1949
dc.date.issued 1949
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/27064
dc.description.abstract This thesis is concerned with the relative reactivity of ethylenic and acetylenic compounds with respect to the addition of halogens. Kinetic studies have been made on bromine addition reactions occurring in the dark at 25°C in acetic acid and aqueous solution. Rate constants for the compounds stilbene, phenyl acetylene, tolane, and the sodium salts of fumaric acid and acetylene dicarboxylic acid have been established. Evidence concerning the properties of the acetylenic linkage has been reviewed and summarised, and the mechanism of halogen addition interpreted in terms of these properties. 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 Halogen addition to acetylenic compounds 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
thesis.degree.name Master of Science en_NZ


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