Tricky SN1 Reactions

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  • Опубліковано 17 січ 2025

КОМЕНТАРІ • 15

  • @peybak
    @peybak 2 роки тому +3

    Hi Victor, I've see a question somewhat similar to the last example. It was on a tough mcat practice passage. I forgot the details but it was an SN1 where the nu could only attack from one side because of steric hindrance, giving a stereospecific product. And many people got it wrong unfortunately.

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  2 роки тому +1

      Yeah, this is a common problem with some of the more advanced questions when students think that if we make a racemic mixture, it will always make the 50-50 mix, while in reality certain molecular features may prevent one attack completely or at least make it very unfavorable like in the last example that you've mentioned.

    • @peybak
      @peybak 2 роки тому +2

      @@VictortheOrganicChemistryTutor Great point. I will definitely be recommending your videos. You're pointing out a lot of problematic areas that trouble the novice students, specially on standardized tests. Cheers!

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  2 роки тому +1

      Thank you! I appreciate any and all help with promoting my channel 😊

  • @luca-jminecraftxx9960
    @luca-jminecraftxx9960 2 роки тому +1

    Truly amazing and helpful examples,keep it up

  • @ramihammoud355
    @ramihammoud355 2 роки тому +1

    this is amazing!!!! im watching all your playlist and im finallly understanding!!1

  • @dereksavastano
    @dereksavastano 9 місяців тому

    Great video bro💪

  • @danielamartinezandrade7378
    @danielamartinezandrade7378 2 роки тому

    Thanks so much!!!

  • @dominicdjan8700
    @dominicdjan8700 Рік тому

    I wish you could draw their stereoisomers

  • @esetesey7346
    @esetesey7346 Рік тому

    On the 1st eg you said 5 mem ring is more stable than 4 mem ring but on the 2nd one you said 6mem ring is more stable how? 🤔
    Thank you!