Acid catalysed acetylene-allene isomerisations

dc.contributor.author	Hei, Siang-King
dc.date.accessioned	2011-03-10T22:53:46Z
dc.date.accessioned	2022-10-25T04:40:09Z
dc.date.available	2011-03-10T22:53:46Z
dc.date.available	2022-10-25T04:40:09Z
dc.date.copyright	1969
dc.date.issued	1969
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/23184
dc.description.abstract	The isomerisation of l-hexyne, 2-hexyne, 3-hexyne, 1,2-hexadiene and 2,3-hexadiene have been studied in solutions of sulphuric acid in sulpholane. The probable mechanism of the isomerisations involving carbonium ions has been outlined. There appears to be no rearrangement of the intermediate carbonium ions involving hydride ion shifts. Free energy changes in the isomerisation were not determined, since equilibration studies could not be carried out due to side reactions during the isomerisations.	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.subject	Isomerism	en_NZ
dc.title	Acid catalysed acetylene-allene isomerisations	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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