Epoxide Opening in Acidic and Basic Conditions

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  • čas přidán 30. 07. 2024
  • In this video we'll look at the epoxide opening in acidic and basic conditions.
    00:00 Intro, TLDR:
    01:35 Opening of epoxides in acidic conditions
    06:12 Opening of epoxides in basic conditions
    #organicchemistry #organicchemistrytutor #epoxides
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Komentáře • 12

  • @VictortheOrganicChemistryTutor

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    • @smalliver365
      @smalliver365 Před 8 měsíci +1

      That's crazy man I have an exam over this tomorrow. You're the best. One simple question if I may. Does 'acidic and basic conditions' correlate to 'acidic opening of epoxides' and 'nucleophilic opening of epoxides' as my professor teaches? he does explain that 'nucleophilic' is also a backside SN2 attack.

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  Před 8 měsíci

      @@smalliver365 Yep. "Basic" opening and "Nucleophilic" opening refer to the same thing when it comes to the opening of epoxides. That's why I pointed it out in the video. It's just the "basic" opening is more popular among professors and textbooks since it gives an easy to remember dichotomy.
      And yes, both proceed through the SN2 mechanism with the inversion of stereochemistry when applicable. I prolly should've mentioned that more explicitly in the video.
      Best of luck tomorrow!

    • @smalliver365
      @smalliver365 Před 8 měsíci

      @@VictortheOrganicChemistryTutor Awesome, thank you so much!

    • @alindajustus2133
      @alindajustus2133 Před 3 měsíci

      @@smalliver365 i also had the same question

  • @amandad.2321
    @amandad.2321 Před 3 měsíci

    Hi Victor, thanks for another great video! My question is how would you go about opening an epoxide ring if it is symmetrical? Thanks for the help!

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  Před 3 měsíci

      If it is symmetrical, it doesn't matter which side you're going to choose. If you're concerned with the stereochemistry, you'll have a 50/50 split opening from each side giving you a pair of stereoisomers (typically, enantiomers, but might be diastereomers depending on the molecule).

  • @user-gn3if7mo2y
    @user-gn3if7mo2y Před 8 měsíci

    what software are you using ?

    • @akshadnimbarte
      @akshadnimbarte Před 8 měsíci

      It’s an app called goodnotes

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  Před 8 měsíci +1

      Not in this video or the vast majority of my other videos... I've used goodnotes to make a few of my videos, but it's by far the least used app I use for my videos. I use up to 8 different apps/software packages to make my content, and I don't see any point in listing them all. What works for me may or may not work for others.

    • @user-gn3if7mo2y
      @user-gn3if7mo2y Před 8 měsíci

      @@VictortheOrganicChemistryTutor I think if you make a video about how you make such useful videos it would be great viictor pro max😅

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  Před 8 měsíci +1

      @@user-gn3if7mo2y I dunno, maybe at some point I'll consider that. But that's not my channel focus, so even if I make a video like that some time in the future, it's not going to be any time soon.