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  2. 2,3-Dimethylbutane - Wikipedia

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

    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 ...

  3. C6H14 - Wikipedia

    en.wikipedia.org/wiki/C6H14

    The molecular formula C 6 H 14 (molar mass: 86.17 g/mol) may refer to: Dimethylbutanes 2,2-Dimethylbutane; 2,3-Dimethylbutane; Hexane; Methylpentanes 2-Methylpentane;

  4. 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 ...

  5. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    For example, compare isobutane (2-methylpropane) and n-butane (butane), which boil at −12 and 0 °C, and 2,2-dimethylbutane and 2,3-dimethylbutane which boil at 50 and 58 °C, respectively. [ 18 ] On the other hand, cycloalkanes tend to have higher boiling points than their linear counterparts due to the locked conformations of the molecules ...

  6. Wurtz reaction - Wikipedia

    en.wikipedia.org/wiki/Wurtz_reaction

    In organic chemistry, the Wurtz reaction, named after Charles Adolphe Wurtz, is a coupling reaction in which two alkyl halides are treated with sodium metal to form a higher alkane. 2 R−X + 2 Na → R−R + 2 NaX. The reaction is of little value except for intramolecular versions, such as 1,6-dibromohexane + 2 Na → cyclohexane + 2 NaBr.

  7. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 Cl 2 or CCl 4). The product is a vicinal dihalide. This type of reaction is a halogenation and an electrophilic addition.

  8. Isovaleraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isovaleraldehyde

    [2] [5] The compound is used as a reactant in the synthesis of a number of compounds. Notably it is used to synthesize 2,3-dimethylbut-2-ene, and is then converted to 2,3-dimethylbutane-2,3-diol and methyl tert-butyl ketone, better known as pinacolone. Pinacolone itself is then used in synthesis for number of pesticides.

  9. 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.