1-Methylcyclohexene is an organic compound, specifically a cyclic alkene. It consists of a six-membered ring (cyclohexene) with a methyl group attached to one of the carbon atoms involved in the double bond.
Structure: The molecule is based on a cyclohexene ring, meaning it has a single double bond within the ring. A methyl group (-CH3) is attached to a carbon directly adjacent to the double bond.
Isomers: 1-Methylcyclohexene can exist as cis- and trans- isomers, although the cis form is less common due to steric hindrance. The cis/trans isomerism is related to the relative position of groups connected to the 1 and 2 carbon atoms relative to the ring plane.
Reactivity: As an alkene, 1-methylcyclohexene undergoes addition reactions at the double bond. Common reactions include hydrogenation, halogenation, hydration, and hydrohalogenation. The methyl group can also influence the regioselectivity of these reactions.
Preparation: It can be prepared through various methods, including the dehydration of 1-methylcyclohexanol or the elimination reaction of a leaving group from a substituted cyclohexane.
Uses: 1-Methylcyclohexene is used as a reagent in organic synthesis.
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