Halogenation of Alkenes | Mechanism | Stereochemistry | Examples

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  • Опубліковано 4 січ 2025

КОМЕНТАРІ • 18

  • @peybak
    @peybak Рік тому +5

    @1:14 Showing the electrons move like that was top notch!

  • @vladmirputinpr
    @vladmirputinpr 9 днів тому

    Your videos are always amazing making everyone like the chemistry!

  • @just_josh_scoups_of_icecream
    @just_josh_scoups_of_icecream 7 місяців тому +5

    Can't believe an explanation this good has so low recognition, this is the probably the only video which explained stereochemistry so well
    Thank u so much i was initially so confused but now its all good thanks to ur amazing explanation

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  7 місяців тому

      Glad it was helpful! My channel is fairly new, so hopefully, more students will find it in the future.

  • @lidyacorrea8860
    @lidyacorrea8860 5 місяців тому

    organic chemistry is a mandatory course for my major, and i underestimated it the entire semester!! the exam is tomorrow and you saved my semester, thank you so much!!

  • @Liam23333-f
    @Liam23333-f 6 місяців тому +2

    the video deserve more views!

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  6 місяців тому

      Tell this to UA-cam algorithm 😂 I do appreciate your support though. I started seriously posting last September but my channel only started to pick up some pace in the spring, so just give it a bit time and I think more students will see these videos.

  • @Nick-jw1gr
    @Nick-jw1gr 7 місяців тому

    Love your videos! You always give amazing tips and give clear explanations

  • @lalayatem3758
    @lalayatem3758 2 місяці тому

    Thank you, this is very insightful! Could please you do a video on total synthesis of a product eg taxol?

  • @ANURAGIITG202
    @ANURAGIITG202 9 місяців тому

    Which app do you use for notes taking ?

  • @melazaskhia9512
    @melazaskhia9512 Рік тому

    help me to answer this question 2-heptanone+iodine, with catalysm NaOH plisss

  • @karola9236
    @karola9236 9 місяців тому

    Thanks

  • @rockubabe
    @rockubabe Рік тому

    In your first example at 5:15, isn't the bond between the C and BR SP3 hybridization? I thought the bond would be flat without coming forward or backward.
    Also, I is more electronegative than Cl, doesn't that mean I should be partial negative? Not partial positive?

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  Рік тому

      Bond cannot have any hybridization. It’s the carbon that’s sp3 hybridized. And precisely because of that it has a tetrahedral geometry.
      No, iodine is not more electronegative than chlorine. Look at your periodic table.