Fused Rings, Bridged Bicyclic and Spiro Compounds, Cis and Trans Decalin, Bredt' s rule

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  • Опубликовано: 25 ноя 2024

Комментарии • 6

  • @Senthilkumar-nf5sp
    @Senthilkumar-nf5sp 4 года назад

    Super fantastic mam

  • @ranjanaladdu3817
    @ranjanaladdu3817 4 года назад

    Thankuu so much mam very nice leature.

  • @amarkrish628
    @amarkrish628 3 года назад

    In naphthalene also we can name as bicyclo[4.4.0]decane . Is possible

  • @Holistichomoeo
    @Holistichomoeo 4 года назад

    Mam fused rings m b to bridge head carbon h to phir wha kyun bredt's rule fail ho gya....I mean wo stable kyun hota h ..hybridisation to uski b sp2 hi ho gai na....
    Plzz reply

    • @Chemistryunplugged
      @Chemistryunplugged  4 года назад

      Hello Bhoomika.. Double bond formation means first a carbocation is generated at bridghead position and carbocation has planar structure which is not feasible for bridged compound while fused ring may get somewhat planar structure and it depends on fused ring size.. This rule is only for bridged compounds.

  • @Senthilkumar-nf5sp
    @Senthilkumar-nf5sp 4 года назад

    Super fantastic mam