How to Analyze Nucleophiles & Electrophiles to Predict EVERY ORGANIC CHEMISTRY REACTION! MCAT O-CHEM

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  • Опубликовано: 1 янв 2025

Комментарии • 22

  • @noahjohnson8389
    @noahjohnson8389 3 года назад +49

    dude I wish I was as passionate about organic chem as you. thought you were going to cry a few times. Love the enthusiasm - video was very helpful!

  • @karilynnwilson8967
    @karilynnwilson8967 3 года назад +42

    best MCAT channel out there

  • @theegress3131
    @theegress3131 11 месяцев назад +3

    This helped SOOO MUCH please keep up the good work!!!

  • @MS-mg3lz
    @MS-mg3lz Год назад +4

    In the last problem, why wouldn't the electrophile react with the carbon bound to oxygen and nitrogen? Since in that case there would be more electronegative atoms pulling charge away from the carbon.

  • @JamieFinan
    @JamieFinan 5 месяцев назад +1

    Really like the simplicity! However, I didn't hear you discuss steric hindrance of electrophilic reactivity (aldehydes = least hindered and most kinetically favored/strongest) or resonance stabilization of your formal charges. Thanks!

  • @GhilledM21
    @GhilledM21 2 года назад +7

    i got so tired of reading jack westin/shem for months and my eyes were kneeling over. really nice to watch videos, and to have something as clear cut as this

  • @curtpiazza1688
    @curtpiazza1688 Год назад +2

    I love the thorough explanations! 😂 🎉 ❤

  • @MegaBaller234
    @MegaBaller234 3 года назад +10

    dude.. thank you

  • @Dustin_-
    @Dustin_- 3 года назад +1

    Thank you for the video

  • @kingofpirates891
    @kingofpirates891 Год назад

    wow thank you so much!

  • @niloofarkh4779
    @niloofarkh4779 2 года назад +1

    thank u very much

  • @nateweinstock4427
    @nateweinstock4427 3 года назад +1

    SO HELPFUL :))

  • @espanadorada7962
    @espanadorada7962 8 месяцев назад

    Your thumbnail has them backwards…

  • @aymanamiera
    @aymanamiera 2 года назад +1

    youre the bestest

  • @harley6659
    @harley6659 3 года назад

    Wouldn’t that phosphate group be sterically hindered so it wouldn’t even react or am I tripping

    • @sciencesimplified3890
      @sciencesimplified3890  3 года назад +2

      Do you mean would the oxygens around the phosphate block any nucleophile from being able to react with the phosphate? If that’s what you mean then I can tell you that nucleophiles are able to reach the phosphate, and this type of reaction is very common (for example adding nucleotides to DNA and RNA, hydrolysis of ATP etc)

    • @harley6659
      @harley6659 3 года назад +1

      @@sciencesimplified3890 yes that’s what I meant. Thank you for clarifying that!

  • @elenagalkina5653
    @elenagalkina5653 3 года назад +11

    good material, but I hope you are not having a stroke

  • @Realbusinessfoundations
    @Realbusinessfoundations Год назад

    thnk u u u u u u u u u uu uu

  • @Kencan254
    @Kencan254 11 месяцев назад

    Too noisy 😊

  • @phrenologisto
    @phrenologisto Год назад +2

    As a 'rule of thumb' you might consider working on losing that phrase from your vocab. Etymology aint pretty (max size of stick youre allowed to beat your wife with = width of your thumb = rule of thumb). Amazing content and cant thank you enough for sharing! By all means, use the phrase. I just know that when I found out what the og rule of thumb was, it stopped feeling right when it slipped out. hard one to lose.