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Iodine Addition to Related Ethylenic Compounds

dc.contributor.authorBythell, Noel John
dc.date.accessioned2011-12-13T21:29:05Z
dc.date.accessioned2022-10-31T22:03:16Z
dc.date.available2011-12-13T21:29:05Z
dc.date.available2022-10-31T22:03:16Z
dc.date.copyright1937
dc.date.issued1937
dc.description.abstractThe addition of halogens to unsaturated compounds according to the equation X₂ + A=B → AX.BX has been gradually accepted to occur by an ionic mechanism. T. M. Lowry early made the suggestion that the reactivity of double bonds was caused by the development of polarisation such as CH₂(+)-CH₂(-) while the halogen molecule dissociated into ions which reacted with this. Activation of the ethylenic compound would take place by means of some catalyst in the gas, liquid, or solid phase. As will be seen, the environment of the double link determines the mode of this polarisation and the ease or tardiness with which it takes place. The molecule of every halogen has an appreciable permanent dipole moment - that of iodine being the greatest. Not only is liquid iodine an ionising solvent, but also iodine in certain ionising solvents has been found to conduct electricity, demonstrating actual ionic dissociation of the molecule.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/27175
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.subjectIodine
dc.subjectChemistry
dc.subjectEthylenic Compounds
dc.titleIodine Addition to Related Ethylenic Compoundsen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineChemistryen_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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