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  2. 3-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/3-Methylcyclohexene

    3-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent adjacent to the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 4-methylcyclohexene .

  3. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.

  4. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    C 6 H 12: 13 isomers: 1-hexene, 2-hexene, 3-hexene, 2-methyl-1-pentene, 3-methyl-1-pentene, ... (a.k.a. trans-2-butene) the methyl groups appear on opposite sides ...

  5. 4-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/4-Methylcyclohexene

    4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.

  6. 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 .

  7. 1-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/1-Methylcyclohexene

    Oxidation of 1-methylcyclohexene catalyzed by cytochrome P450 yields a 2:1 mixture of hydroxylation to epoxidation products. [4] The stereochemistry of hydroformylation has been examined using 1-methylcyclohexene. The main product has the formyl group on the less substituted alkene-carbon, trans with respect to the methyl substituent. [5]

  8. trans-3-Methyl-2-hexenoic acid - Wikipedia

    en.wikipedia.org/wiki/Trans-3-methyl-2-hexenoic_acid

    trans-3-Methyl-2-hexenoic acid (TMHA) is an unsaturated short-chain fatty acid that occurs in sweat secreted by the axillary apocrine glands of Caucasians and some Asians. [1] Hexanoic acids such as TMHA have a hircine odor. Of the fatty acids contributing to Caucasian men's underarm odor, TMHA has the most prominent odor. [2]

  9. 3-Hexyne - Wikipedia

    en.wikipedia.org/wiki/3-Hexyne

    3-Hexyne is the organic compound with the formula C 2 H 5 CCC 2 H 5. This colorless liquid is one of three isomeric hexynes. 3-Hexyne forms with 5-decyne, 4-octyne, and 2-butyne a series of symmetric alkynes. It is a reagent in organometallic chemistry. [1] Structure of the coordination complex NbCl 3 (dimethoxyethane)(3-hexyne). [2]