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  2. 2,2-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylbutane

    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.

  3. Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutane

    Dimethylbutane (DMB) may refer to: 2,2-Dimethylbutane; 2,3-Dimethylbutane; See also. Dimethylbutanol This page was last edited on 1 April 2021, at ...

  4. 2,3-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylbutane

    2,3-Dimethylbutane is an isomer of hexane. It has the chemical formula (CH 3) 2 CHCH(CH 3) 2. It is a colorless liquid which boils at 57.9 °C. References

  5. Dimethylbutene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutene

    This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

  6. DMDNB - Wikipedia

    en.wikipedia.org/wiki/DMDNB

    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.

  7. 2,3-Dimethyl-1-butene - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethyl-1-butene

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  8. Pinacolone - Wikipedia

    en.wikipedia.org/wiki/Pinacolone

    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. It also is generated by ketonization of pivalic acid and acetic acid or acetone over metal oxide catalysts. 3-Methylbutanal is a starting material for 2,3-dimethyl-2-butene, which in turn is ...

  9. Dimethylbutadiene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutadiene

    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.