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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. Isobutyl chloride - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_chloride

    Isobutyl chloride (1-chloro-2-methylpropane) is an organochlorine compound. It is a chlorinated derivative of isobutane. Synthesis

  4. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    In Figure 6, 2-chloro-2,3-dimethylbutane is stabilized through hyperconjugation from electron donation from σ C-H into σ* C-Cl, but both C–H and C–Cl bonds are weakened. A molecular orbital diagram shows that the mixing of σ C–H and σ* C–Cl in 2-chloro-2,3-dimethylbutane lowers the energy of both the orbitals (Figure 7).

  5. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cyclo alkyl -" (e.g. "cyclohexyl-") or for benzene, "phenyl-".

  6. 1-Chlorobutane - Wikipedia

    en.wikipedia.org/wiki/1-Chlorobutane

    1-Chlorobutane is an alkyl halide with the chemical formula CH 3 (CH 2) 3 Cl. It is a colorless, flammable liquid. It is a colorless, flammable liquid. Preparation and reactions

  7. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    3D structure A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [ 1 ] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes.

  8. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  9. Isopentane - Wikipedia

    en.wikipedia.org/wiki/Isopentane

    The traditional name isopentane was still retained in the 1993 IUPAC recommendations, [5] [6] but is no longer recommended according to the 2013 recommendations. [1] The preferred IUPAC name is the systematic name 2-methylbutane. An isopentyl group is a subset of the generic pentyl group. It has the chemical structure -CH 3 CH 2 CH(CH 3) 2.