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  2. 2,3-Dimethylbutane - Wikipedia

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

    2,3,4-Trimethylpentane Tetra- tert -butylmethane Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

  3. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    Figure 5 shows 2-chloro-2,3-dimethylbutane in a sawhorse projection with chlorine and a hydrogen anti-periplanar to each other. Syn-periplanar or synperiplanar is similar to anti-periplanar. In the syn-periplanar conformer, the A and D are on the same side of the plane of the bond, with the dihedral angle of A−B and C−D between +30° and ...

  4. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    In 1967 the group of George A. Olah obtained NMR spectra of tetramethylethylenebromonium ions by dissolving 2,3-dibromo-2,3-dimethylbutane in magic acid at −60 °C. [5] The spectrum for the corresponding fluorine compound on the other hand was consistent with a rapidly equilibrating pair of β-fluorocarbocations.

  5. Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutane

    Download as PDF; Printable version; In other projects ... move to sidebar hide. Dimethylbutane (DMB) may refer to: 2,2-Dimethylbutane; 2,3-Dimethylbutane ; See also ...

  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. 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 ...

  8. 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.

  9. 2,3-Dimethyl-1-butene - Wikipedia

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

    2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene , it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene .