All About Reductive Amination

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  • Опубликовано: 26 ноя 2024
  • joechem.io/vid... for video on jOeCHEM and attached worksheet + solution (below video on jOeCHEM aka the link).
    Worksheet: worksheets.joec...
    Worksheet Solution: worksheets.joec...
    Worksheet Solution Walkthrough video: joechem.io/vid...
    Study Guide: N/a (Joe's working on it!)
    In this video, we take a look at Reductive Amination--its mechanism and how to predict products successfully. What's awesome is, if you put in the work back when we worked with imines (joechem.io/vid...) this will be very familiar and a cakewalk for you.
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Комментарии • 16

  • @user8_8
    @user8_8 Год назад +1

    Very helpful explanation, thank you so much!!

  • @shoutitallloud
    @shoutitallloud 4 года назад +15

    You look too young for mr.Heisenberg... But anyway, here's your phenyl-propan-2-one.

  • @NikOthman
    @NikOthman 3 года назад +3

    👍👍👍Next pls how to synthesis 1phenyl2propanone?? Thank you

  • @doaamahmoud7114
    @doaamahmoud7114 2 года назад +2

    Thanks that was so much helpful!!!

  • @Piocoto123
    @Piocoto123 10 месяцев назад

    Thank you for the video! Do you know what does the boron ends up turning into? some borate?

  • @kobold7763
    @kobold7763 2 года назад +1

    So would this reaction work for reductive animation of n,n diethylamine to n,n Diethylmethylamine?

  • @ajx8571
    @ajx8571 3 года назад +1

    This is awesome bro thank you.

  • @skriosorgooeltkhgo4068
    @skriosorgooeltkhgo4068 Год назад

    Can't you use LAH if you extract and purify the imine instead of doing a one pot reaction?

  • @directionerhere932
    @directionerhere932 2 года назад

    how to do this mechanism if we're doing it in neutral condition. Amine directly attacks the aldehyde, but the double bond of the carbonyl wont shift right?

  • @erikdejong4509
    @erikdejong4509 2 года назад

    When you add your NaCNBH3 do you still need to add acid to protonate the N or is there still H3O in your solution

  • @spurti
    @spurti 2 года назад

    Hii I have a question can we produce 1° aromatic amines from gabriel pthalimide synthesis???like aniline for example.

  • @krish1596
    @krish1596 3 года назад +1

    Can we use H2, raney Ni? Instead of nabh3cn?

    • @jOeCHEM
      @jOeCHEM  3 года назад

      In theory, that would perform a reduction, but I have personally never seen something used in place of nabh3cn for this reaction. So I would say stick with nabh3cn unless your instructor uses something different.

  • @jhyland87
    @jhyland87 2 года назад

    well done. subscribed

  • @ghadasalah1937
    @ghadasalah1937 2 года назад

    thankkkkkkkkkkkkk uuuuu

    • @jOeCHEM
      @jOeCHEM  2 года назад +1

      yourrrrrrrrrrrrr welcomeeeee (thanks for watching!)