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  2. 3-Methylhexane - Wikipedia

    en.wikipedia.org/wiki/3-Methylhexane

    3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]

  3. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the " -ene " suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond .

  4. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Very often, cis–trans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.

  5. Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexene

    3-Methylcyclohexene; 4-Methylcyclohexene This page was last edited on 18 November 2024, at 14:45 (UTC). Text is available under the Creative Commons Attribution ...

  6. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    The hexynes are a subgroup from the group of alkynes.It consists of several isomeric compounds having the formula C 6 H 10.. The linear and branched members are: 1-Hexyne (n-butylacetylene)

  7. 2-Hexyne - Wikipedia

    en.wikipedia.org/wiki/2-Hexyne

    2-Hexyne can be semihydrogenated to yield 2-hexene or fully hydrogenated to hexane. [3] With appropriate noble metal catalysts it can selectively form cis-2-hexene. [4] 2-Hexyne can act as a ligand on gold atoms. [5] With strong sulfuric acid, the ketone 2-hexanone is produced. However this reaction also causes polymerization and charring. [6]

  8. C6H12 - Wikipedia

    en.wikipedia.org/wiki/C6H12

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  9. Methylenecyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylenecyclohexane

    2 Structure. 3 See also. ... [2] [3] It can also be synthesized as a side product of the dehydration of 2-methylcyclohexanol into 1-methylcyclohexene. Structure