Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/76910
DC FieldValue
dc.titleRotational isomerism in 2,3-dinitro-2,3-dimethylbutane
dc.contributor.authorTan, B.-G.
dc.contributor.authorChia, L.H.L.
dc.contributor.authorHuang, H.-H.
dc.contributor.authorKuok, M.-H.
dc.contributor.authorTang, S.-H.
dc.date.accessioned2014-06-23T05:48:36Z
dc.date.available2014-06-23T05:48:36Z
dc.date.issued1984
dc.identifier.citationTan, B.-G.,Chia, L.H.L.,Huang, H.-H.,Kuok, M.-H.,Tang, S.-H. (1984). Rotational isomerism in 2,3-dinitro-2,3-dimethylbutane. Journal of the Chemical Society, Perkin Transactions 2 (8) : 1407-1413. ScholarBank@NUS Repository.
dc.identifier.issn1472779X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76910
dc.description.abstractI.r. and Raman spectra of 2,3-dinitro-2,3-dimethylbutane (in the solid and solution states) are reported and assignments of frequencies made. Comparison of the Raman and i.r. spectra of the solid shows that the compound exists in the graucae-conformation in the solid state. Dipole moments in different solvents (benzene, carbon tetrachloride, dioxane, and cyclohexane) at different temperatures and molar Kerr constants (in carbon tetrachloride and benzene) are also reported. Analysis of the physical data shows that, at 25°C, 2,3-dinitro-2,3-dimethylbutane exists as a rotameric mixture of 42% gauche and 58% trans in carbon tetrachloride solution, and 79% gauche and 21% trans in benzene solution. Solvent effects are also discussed.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleJournal of the Chemical Society, Perkin Transactions 2
dc.description.issue8
dc.description.page1407-1413
dc.identifier.isiutNOT_IN_WOS
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