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1,3,5 trimethyl cyclohexane on bromination under uv light then how many monobrominated products will be obtained by this reacn?
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1,3,5 trimethyl cyclohexane on bromination under uv light then how man...
Bromination of 1,3,5 Trimethyl Cyclohexane



  • Bromination: The addition of a bromine atom to an organic molecule

  • 1,3,5 Trimethyl Cyclohexane: A cyclohexane molecule with three methyl groups attached to non-adjacent carbons

  • UV light: A form of electromagnetic radiation that can cause reactions to occur



Bromination Mechanism



  • Bromine reacts with the double bond in the cyclohexane ring

  • A bromine radical is formed, which can then react with a hydrogen atom on the ring to form HBr and a cyclohexyl radical

  • The cyclohexyl radical can then react with another bromine molecule to form the monobrominated product



Monobrominated Products



  • There are three possible sites for bromination on the 1,3,5 trimethyl cyclohexane molecule

  • Each site will produce a different monobrominated product:


    • 1-bromo-1,3,5-trimethylcyclohexane

    • 3-bromo-1,3,5-trimethylcyclohexane

    • 5-bromo-1,3,5-trimethylcyclohexane


  • The products will be formed in equal amounts if the reaction conditions are the same



Conclusion



  • When 1,3,5 trimethyl cyclohexane is brominated under UV light, three monobrominated products will be formed

  • The products will be formed in equal amounts

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1,3,5 trimethyl cyclohexane on bromination under uv light then how many monobrominated products will be obtained by this reacn?
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