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  2. 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. It is a precursor to the commercial fragrance tonalide. [1]

  3. Dimethylbutene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutene

    3,3-Dimethyl-1-butene; 2,3-Dimethyl-2-butene This page was last edited on 20 October 2020, at 08:55 (UTC). Text is available under the Creative Commons Attribution ...

  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. 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.

  6. Dimethylbutadiene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutadiene

    Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH 3) 2 C 4 H 4. It is colorless liquid which served an important role in the early history of synthetic rubber. It is now a specialty reagent.

  7. File:2,3-dimethylbutane.svg - Wikipedia

    en.wikipedia.org/wiki/File:2,3-dimethylbutane.svg

    English: Chemical structure of 2,3-dimethylbutane. Français : Représentation du 2,3-Diméthylbutane. ... Add a one-line explanation of what this file represents.

  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. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    2-methylprop-1-ene In the chemical structures above, the small blue numbers in the structure images are the numbering of the atoms in the main backbone chain of the molecules. Other organic compounds have the formula C 4 H 8 , namely cyclobutane and methylcyclopropane , but are not alkenes and do not fall under the name butene .