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2,3-Dimethylbutane Skeletal formula of 2,3-dimethylbutane with some implicit hydrogens shown: Ball and stick model of 2,3-dimethylbutane: Names Preferred IUPAC name.
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2,2-Dimethylbutane, trivially known as neohexane at William Odling's 1876 suggestion, [4] is an organic compound with formula C 6 H 14 or (H 3 C-) 3-C-CH 2-CH 3. It is therefore an alkane , indeed the most compact and branched of the hexane isomers — the only one with a quaternary carbon and a butane (C 4 ) backbone.
DMDNB, or also DMNB, chemically 2,3-dimethyl-2,3-dinitrobutane, is a volatile organic compound used as a detection taggant for explosives, mostly in the United States where it is virtually the only such taggant in use.
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Dimethylbutane; Hexanol This page was last edited on 1 April 2021, at ... About Wikipedia; Disclaimers; Contact Wikipedia; Code of Conduct; Developers; Statistics;
Dimethylbutadiene readily undergoes Diels-Alder reactions and reacts faster than 1,3-butadiene.Its effectiveness in this reaction is attributed to the stabilization of the cis-conformation owing to the influence of the methyl groups on the C2 and C3 positions.
Most famously, at least in the classroom, pinacolone arises by the pinacol rearrangement, which occurs by protonation of pinacol (2,3-dimethylbutane-2,3-diol). [4] Industrially pinacolone is made by the hydrolysis of 4,4,5-trimethyl-1,3-dioxane, which is the product of isoprene and formaldehyde via the Prins reaction.