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The kinetics of bromine addition to allyl halides in carbon tetrachloride

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dc.contributor.author Caradus, John Nelson
dc.date.accessioned 2011-12-13T21:27:00Z
dc.date.accessioned 2022-10-31T21:28:35Z
dc.date.available 2011-12-13T21:27:00Z
dc.date.available 2022-10-31T21:28:35Z
dc.date.copyright 1947
dc.date.issued 1947
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/27099
dc.description.abstract Although the addition of halogens at the double bond is one of the most general reactions of unsaturated compounds, there is extreme variation of reactivity displayed by different unsaturated compounds towards halogens. Considerable complexity is revealed by Kinetic investigations, and the celerity of halogen addition to certain olefins (e.g. ethylene and styrene) is deceptive if taken to signify that the reaction mechanism is simple. As well as the internal structure of the compound itself, there are considerable effects produced in certain reactions due to the external factors temperature, light, solvent, and catalysts. 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 The kinetics of bromine addition to allyl halides in carbon tetrachloride 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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