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  2. 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 .

  3. C6H12 - Wikipedia

    en.wikipedia.org/wiki/C6H12

    Download QR code; Print/export Download as PDF; Printable version; In other projects ... 2-Hexene; 3-Hexene; Methylpentenes. 2-Methyl-1-pentene;

  4. Methylenecyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylenecyclohexane

    Download as PDF; Printable version; In other projects Wikimedia Commons; ... [2] [3] It can also be ... Structure Methylenecyclohexane ...

  5. 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]

  6. 1-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/1-Methylcyclohexene

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

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    ch 2 =ch 2 + ch 3 ch=chch 32 ch 2 =chch 3 Transition metal catalyzed hydrovinylation is another important alkene synthesis process starting from alkene itself. [ 31 ] It involves the addition of a hydrogen and a vinyl group (or an alkenyl group) across a double bond.

  8. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    3 C 6 H 6 + CHCl 3 → Ph 3 CH + 3 HCl. Alternatively, benzene may react with carbon tetrachloride using the same catalyst to obtain the triphenylmethyl chloride–aluminium chloride adduct which is then treated with diethyl ether for 24 hours at room temperature and hydrolyzed with concentrated hydrochloric acid: [3] 3 C 6 H 6 + CCl 4 + AlCl 3 ...

  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]