The Wittig Reaction

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  • Опубліковано 31 січ 2025

КОМЕНТАРІ • 19

  • @jeremyharrison9265
    @jeremyharrison9265 4 роки тому +10

    you are awesome, just came across your channel and these are one of the best explanations I have seen. Thanks!!

    • @jOeCHEM
      @jOeCHEM  4 роки тому

      Jeremy, thanks a ton, man! I've since made a second video on this topic ua-cam.com/video/PiFpT2Zxwhw/v-deo.html
      (I go a bit more in depth because you can get a different double bond if you have a ylide thats attached next door to an aromatic system). Make sure to check out joechem.io/videos/38 where I have a worksheet + solutions linked (literally for free).
      And if you subscribe that would be H U G E L Y appreciated :)

  • @DaBaaaang
    @DaBaaaang 2 роки тому +13

    You remind me of Joey from Friends, just smarter. Thanks for your work bro.

    • @Tina-xw8mb
      @Tina-xw8mb 4 місяці тому +1

      This! 👆

    • @mitcho5452
      @mitcho5452 3 місяці тому +1

      I WAS JUST THINKING THIS AHH😂

  • @mohammadsaifullahkhan53
    @mohammadsaifullahkhan53 3 роки тому +4

    This channel is awesome!!!

  • @kenhagiya565
    @kenhagiya565 2 роки тому +3

    JoeChem saving my ass once again. Thank you for the videos!

  • @tharushimunasinghe1716
    @tharushimunasinghe1716 8 місяців тому +1

    Thank you soomuch ❤

  • @meryammaryam4348
    @meryammaryam4348 2 роки тому +2

    Thank you my friend🤗

  • @Sophia-rl5ph
    @Sophia-rl5ph 2 роки тому +1

    Thank you so much, I really appreciate you!

  • @stormydoctor9009
    @stormydoctor9009 10 місяців тому +1

    hi you know for the lda how it deprotonates less sterically hindered alpha hydrogens why did it deprotonate the sterically hindered alpha H's

    • @stormydoctor9009
      @stormydoctor9009 10 місяців тому

      why not just use NaOme if you deprotonated the least sterically hindered H's

    • @jOeCHEM
      @jOeCHEM  10 місяців тому

      It does because LDA is VERY large, so it is hard to reach more "crowded" alpha H's. So it is lazy and opts for alpha H's that are less sterically hindered, aka more accessible.
      Something like NaOMe is MUCH smaller, so it can access more "crowded" alpha H's.

  • @irem9955
    @irem9955 10 місяців тому +1

    would be better if you also solve questions which wittig is involved as a step. more complex questions pls

    • @jOeCHEM
      @jOeCHEM  10 місяців тому

      Check out ua-cam.com/video/PiFpT2Zxwhw/v-deo.html

  • @LuoanaBelénMuiñoSosa
    @LuoanaBelénMuiñoSosa Місяць тому +1

    I never thought Joey Tribbiani would teach me organic chemistry lol

    • @jOeCHEM
      @jOeCHEM  Місяць тому +1

      What's so funny is that I've been getting that comparison since I was 5 years old lol

  • @aminazeh
    @aminazeh Місяць тому

    ordinarry thinks

  • @francoislaflammeawono317
    @francoislaflammeawono317 3 роки тому

    Je ne suis pas d’accord avec ta réaction mon type