Wolff Rearrangement

Поделиться
HTML-код
  • Опубликовано: 29 окт 2024

Комментарии • 8

  • @parakhmody1413
    @parakhmody1413 7 лет назад +5

    +AK LECTURES
    The resonance structure on the right for diazoketone is incorrect; the middle nitrogen has five bonds. Also, the middle nitrogen should have positive charge and the end nitrogen should have negative charge.
    Similarly, resonance structure on the right for diazomethane is incorrect; for the same reasons mentioned above.

  • @rishisiva2363
    @rishisiva2363 Год назад

    this the best tutorial i ever seen , be your best...

  • @raudreyagupta2599
    @raudreyagupta2599 3 года назад

    The resonance structure of diazomethane on the right is wrong. Nitrogen can't have 5 bonds. Instead, one of the triple bonds must break, and the middle N gets a + charge, and the N to the right gets a - charge.

  • @madhusmitasahoo5555
    @madhusmitasahoo5555 6 лет назад +2

    Chloride ion is not a strong base how can it abstract an alpha hydrogen.since chloride ion is a congugate base of hcl which is a strong acid

    • @debapratimnag1950
      @debapratimnag1950 5 лет назад +1

      cuz it's abstracting a fucking acidic hydrogen ffs.

  • @김소연-g4i7p
    @김소연-g4i7p 3 года назад

    What is a driving force to arrange R?

  • @sachdev2312
    @sachdev2312 9 лет назад +1

    thank you so much!!!! :)

  • @김소연-g4i7p
    @김소연-g4i7p 3 года назад

    Acid chloride -> Acyl chloride