Intro to Markovnikov Additions to Double Bonds--Using Binary Acids and Water

Поделиться
HTML-код
  • Опубликовано: 29 окт 2024

Комментарии • 8

  • @andre816
    @andre816 5 месяцев назад +1

    THANK YOU SO MUCH

  • @kenhagiya565
    @kenhagiya565 2 года назад +1

    Awesome, so easy to understand!
    There's just one thing I'm confused on: 12:00 where you mention an intramolecular methyl shift.
    I know previously that protons can move around a molecule so that it's more stable, etc.. but how does the methyl shift? I thought it is a bad leaving group. Is it floating in solution for a while before shifting? Is it "hard" or "unfavourable" to do such a methyl shift?
    Sorry, the idea was a bit unintuitive to me.. thanks Joe!

    • @jOeCHEM
      @jOeCHEM  2 года назад +1

      Hi, Ken! Thanks for watching and being a jOeCHEMist! In terms of carbocation shifts, yes you can certainly have hydride (aka "proton" even though you're technically moving H:- & not H+, so its a hydride shift, not a proton shift), BUT you can also move methyl groups in the event you're next door to a quaternary carbon. Methyl groups, although they're larger than hydride atoms, are "small enough" to move if it leads to a more stable result in terms of the carbocation.
      For a deeper explanation on carbocation shifts, see the video below!
      ruclips.net/video/hwQ8cFd3d88/видео.html

    • @kenhagiya565
      @kenhagiya565 2 года назад +1

      @@jOeCHEM Thanks so much for the help!

  • @Badgerbahalwan
    @Badgerbahalwan 3 года назад

    Thanks for the lesson G

  • @congdao3042
    @congdao3042 3 года назад +1

    I lmaoed at the intro

  • @omgvideos9237
    @omgvideos9237 Год назад

    Dinguerie bb