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Halogen substitution in aromatic compounds

dc.contributor.authorSwindale, Leslie Denis
dc.date.accessioned2011-03-10T22:51:55Z
dc.date.accessioned2022-10-25T04:29:57Z
dc.date.available2011-03-10T22:51:55Z
dc.date.available2022-10-25T04:29:57Z
dc.date.copyright1950
dc.date.issued1950
dc.description.abstractIt is a feature of the chemistry of aromatic compounds that halogens substitute in the ring much more easily than they add. In fact substituent groups have similar effects in aromatic substitution as they have in addition to unsaturated compounds. We find that we can postulate similar mechanisms for both types. Let us them examine the principles which govern these mechanisms:- (1) Condition of the Halogen. Firstly it appears positively established that halogenation represents an electrophilic mode of attack. There is much experimental evidence in support of this, including:- (a) Bromine substitution is accelerated by electron repelling groups in the molecule and retarded by electron attracting groups.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/23161
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.rights.holderAll rights, except those explicitly waived, are held by the Authoren_NZ
dc.rights.licenseAuthor Retains Copyrighten_NZ
dc.rights.urihttps://www.wgtn.ac.nz/library/about-us/policies-and-strategies/copyright-for-the-researcharchive
dc.subjectHalogenationen_NZ
dc.titleHalogen substitution in aromatic compoundsen_NZ
dc.typeTexten_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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