Structure and reactivity in the naphthalene series: monobromo - peri-alkylnaphthalene isomer distributions

dc.contributor.author	Lewis, I. K.	en
dc.date.accessioned	2014-06-23T09:54:22Z
dc.date.available	2014-06-23T09:54:22Z
dc.date.issued	1965	en
dc.description.abstract	1,8-Dimethylnaphthalene, perinaphthane and pleiadene were synthesized to form, with acenaphthene, a group of structurally analogous hydrocarbons. Acenaphthene was brominated under a variety of conditions and the distributions of the product isomers were measured by vapor phase chromatography. A selection of the brominating conditions was then tried on the group of hydrocarbons in an endeavour to relate the isomer distributions to the structural differences between the hydrocarbons. Finally, pairs of the hydrocarbons were brominated to determine their order of reactivity. The inferences that may be drawn from the results are discussed together with their reproducibility and reliability.	en
dc.identifier.uri	http://hdl.handle.net/10092/9293
dc.identifier.uri	http://dx.doi.org/10.26021/6018
dc.language.iso	en
dc.publisher	University of Canterbury. Chemistry	en
dc.relation.isreferencedby	NZCU	en
dc.rights	Copyright I. K. Lewis	en
dc.rights.uri	https://canterbury.libguides.com/rights/theses	en
dc.title	Structure and reactivity in the naphthalene series: monobromo - peri-alkylnaphthalene isomer distributions	en
dc.type	Theses / Dissertations
thesis.degree.discipline	Chemistry
thesis.degree.grantor	University of Canterbury	en
thesis.degree.level	Doctoral	en
thesis.degree.name	Doctor of Philosophy	en
uc.bibnumber	347534
uc.college	Faculty of Science	en

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