Acid Catalyzed Epoxide Ring Opening

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  • Опубліковано 15 гру 2024

КОМЕНТАРІ • 23

  • @inessa255
    @inessa255 9 років тому +7

    the explanation of this was beyond phenomenal. thank you for helping me to understand! wish you were my professor

  • @aryakaran2743
    @aryakaran2743 3 роки тому +2

    This video is helpful after 6 years too.. thanks for providing the clarity of the topic and being on point... I have my exam day after tomorrow 🙃🙃

  • @Danoroxursox13
    @Danoroxursox13 9 років тому +5

    don't bases, such as Cl-, attack on the least substituted carbon?

    • @tarunyadav2765
      @tarunyadav2765 2 роки тому +1

      Cl- will attack least substituted carbon when it is base catalysed.
      But in acid catalysed + plus charge on O is unstable so O will break any one bond (that will cause more + charge on carbon atom)

  • @sweetness583
    @sweetness583 3 місяці тому

    I thought SN2 reactions didn't happen at tertiary carbons.

  • @sophiecantelope713
    @sophiecantelope713 3 роки тому +1

    THANK YOU this is what i needed, now where can I find the base catalyzed???

    • @Clutchprep
      @Clutchprep  2 роки тому

      Hey there! You can learn that here: www.clutchprep.com/organic-chemistry/epoxide-reactions

  • @1314Fher
    @1314Fher 5 років тому +3

    This makes so much more sense now! Thank you so much T.T

  • @ramasamykuppusamy7974
    @ramasamykuppusamy7974 4 роки тому +1

    Is it sn2 or sn1 mechanism

    • @Clutchprep
      @Clutchprep  4 роки тому +1

      Hey there! The nucleophilic attack will be considered SN1 since Cl attacks the more substituted side. :)

  • @songoku362
    @songoku362 3 роки тому +1

    Why the nucleophile attack to the most substituted carbon atom

    • @Clutchprep
      @Clutchprep  3 роки тому +1

      The nucleophile attacked the most substituted carbon atom because it has the most positive character. Hope that helps! :)

    • @SourajeetSahoo
      @SourajeetSahoo 27 днів тому

      How it has the most positive charge ?

    • @songoku362
      @songoku362 27 днів тому

      ​Due to inductive effect​ the density of +ve charge increases and makes it unstable which prefers for acid catalyzed reaction thus base attacks easily.@@SourajeetSahoo

    • @SourajeetSahoo
      @SourajeetSahoo 26 днів тому

      @@songoku362 due to inductive effect +I... positive charge decreases...

  • @danielgladish2502
    @danielgladish2502 4 роки тому +1

    Good video showing the arrow pushing, but the title says this is "acid catalyzed". You should have your acid reformed in the product no?

    • @Clutchprep
      @Clutchprep  4 роки тому +1

      Hey Daniel! That's correct. Most of the time, mechanisms don't show catalysts being reformed anymore. I hope this helps! :)

  • @melodymix9495
    @melodymix9495 Рік тому

    Thank you

  • @estellaque8615
    @estellaque8615 8 років тому +3

    Nice video... The olcohol tho
    😂

    • @Clutchprep
      @Clutchprep  8 років тому +1

      Thanks! Happy to help! :)

  • @phoenixll9858
    @phoenixll9858 2 роки тому

    😍👍👍👍👍👍👍👍