Hydrohalogenation of Alkenes

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  • Опубліковано 21 гру 2024

КОМЕНТАРІ • 13

  • @steveng724
    @steveng724 7 місяців тому

    Hello Mr. Victor , since the hydrogen and halogen can be placed anywhere since its not a syn addition if there were 2 chiral centers you would draw 4 stereoisomers for number 2 16:30 ( the cyclopentane ) ?

  • @ttnylamb4525
    @ttnylamb4525 11 місяців тому

    at 16:30 can't you do a ring expansion as well?

  • @AlJalilaAlMukhaini
    @AlJalilaAlMukhaini 8 місяців тому

    Thank you so much ❤️❤️❤️❤️❤️❤️❤️❤️

  • @ttnylamb4525
    @ttnylamb4525 11 місяців тому

    Great video!

  • @steveng724
    @steveng724 7 місяців тому

    If the chiral center existed before hydrohalogenation , would it still be factored in the number of stereoisomers? Like if there were 2 new chiral centers made and 1 there before hydrohalogenation would there be 2^3 stereoisomers or 2^2?

    • @steveng724
      @steveng724 7 місяців тому

      also if we consider old chiral centers why is that?

    • @steveng724
      @steveng724 7 місяців тому

      the possible stereoisomers that are valid products are only the absolute configurations of the new chiral centers you create through hydrohalogenation right?

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  7 місяців тому

      This is too broad of a statement/question. You always need to consider the structure of your substrate. Is it chiral or enantiomerically pure? Are there any carbocation rearrangements that may create or erase chiral centers? Are we making or destroying any elements of symmetry?
      Always consider the starting material and don't try to come up with the "universal solution" -- it doesn't exist.

  • @hilal8674
    @hilal8674 2 місяці тому

    👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻👏🏻