Cyclohexene

From WikiMD's Wellness Encyclopedia

Cyclohexene[edit | edit source]

Cyclohexene is an organic compound with the formula C₆H₁₀. It is a colorless liquid with a sharp smell. Cyclohexene is a member of the alkene family, characterized by the presence of a carbon-carbon double bond.

Structure and Properties[edit | edit source]

Cyclohexene is a six-membered ring compound with one double bond. The presence of the double bond makes it unsaturated, and it is more reactive than its saturated counterpart, cyclohexane. The molecular geometry around the double bond is trigonal planar, which affects its chemical reactivity.

Physical Properties[edit | edit source]

  • Molecular formula: C₆H₁₀
  • Molar mass: 82.15 g/mol
  • Density: 0.811 g/cm³
  • Boiling point: 83 °C (181 °F)
  • Melting point: -103.5 °C (-154.3 °F)

Chemical Properties[edit | edit source]

Cyclohexene is more reactive than cyclohexane due to the presence of the double bond. It can undergo typical alkene reactions such as:

Synthesis[edit | edit source]

Cyclohexene can be synthesized through several methods:

Dehydration of Cyclohexanol[edit | edit source]

One common method is the dehydration of cyclohexanol using an acid catalyst such as sulfuric acid or phosphoric acid. The reaction proceeds as follows:

C₆H₁₁OH → C₆H₁₀ + H₂O

This reaction is an example of an elimination reaction, specifically an E1 mechanism.

Partial Hydrogenation of Benzene[edit | edit source]

Cyclohexene can also be produced by the partial hydrogenation of benzene using a suitable catalyst under controlled conditions.

Applications[edit | edit source]

Cyclohexene is used in various industrial applications:

  • As an intermediate in the production of adipic acid, which is a precursor for nylon synthesis.
  • In the manufacture of cyclohexanol and cyclohexanone, which are important intermediates in the production of nylon.
  • As a solvent and a starting material for various chemical syntheses.

Safety and Handling[edit | edit source]

Cyclohexene is flammable and should be handled with care. It can form explosive peroxides upon prolonged exposure to air. Proper storage conditions include keeping it in a cool, dry place away from light and air.

See Also[edit | edit source]

References[edit | edit source]

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