Michael Addition Reaction Mechanism

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  • čas přidán 9. 05. 2018
  • This organic chemistry video tutorial provides a basic introduction into the michael addition reaction mechanism which consist of a michael donor / nucleophile and a michael acceptor / electrophile. The michael donor is resonance stabilized enolate ion and the michael acceptor is usually an alpha beta unsaturated aldehyde or ketone.
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Komentáře • 57

  • @TheOrganicChemistryTutor
    @TheOrganicChemistryTutor  Před 6 měsíci +2

    Final Exams and Video Playlists: www.video-tutor.net/

  • @augustineakor5004
    @augustineakor5004 Před 5 lety +126

    You've been so helping that i let long ads run through so you some how get paid. Not enough but it's the least i can do to say thank you!

  • @pronounceitpro1073
    @pronounceitpro1073 Před 5 lety +73

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  • @danielpugh2660
    @danielpugh2660 Před 3 lety +21

    I appreciate your videos so much. You are truly saving so many people’s grades. Thank you so much for making these available.

  • @ItsMe-kv9yq
    @ItsMe-kv9yq Před rokem +4

    Thanks to this dude, I ended up with As in both orgo 1 and 2. I appreciate you sm!!

  • @shatabdichanda636
    @shatabdichanda636 Před 4 lety +2

    More than awesome.very helpful..subscribed to your channel. 🙇‍♀️

  • @derrickmutuma7721
    @derrickmutuma7721 Před rokem +1

    Your videos are so helpful

  • @janaequinones3693
    @janaequinones3693 Před 6 lety +6

    What’s crazy is that everything you’ve been posting lately I was looking for 3 months ago when I was struggling in orgo 2 😩

    • @txqwx
      @txqwx Před 2 lety

      do u know john quinones ???

  • @jonathansanchez8802
    @jonathansanchez8802 Před 3 lety +1

    Getting an A for sure with this guy

  • @priyasharma-ki4mq
    @priyasharma-ki4mq Před 4 lety

    Thanku soo much sir very nice explained

  • @PunmasterSTP
    @PunmasterSTP Před rokem +1

    I had no idea (or totally forgot) about the difference in attack between weak and strong bases. Thanks for another very high-quality demonstration!

    • @lilbanana6159
      @lilbanana6159 Před rokem +1

      hey! why did the weak base attack at the beta carbon and not at the carbon hving the oxygen?

    • @PunmasterSTP
      @PunmasterSTP Před rokem +1

      @@lilbanana6159 I think that's a great question! I just googled it and found a page on LibreTexts that had this to say:
      If the nucleophile is a weak base, such as alcohols or amines, then the 1,2 addition is usually reversible. This means the competition between 1,2 and 1,4 addition is under thermodynamic control. In this case 1,4-addition dominates because the stable carbonyl group is retained.

    • @shreemoyde7031
      @shreemoyde7031 Před rokem +1

      I have a question. Why is not the nucleophile adding in alpha position? Why doesn't the alpha Carbon become positive since the keto group is an electron withdrawing group?

    • @PunmasterSTP
      @PunmasterSTP Před 11 měsíci +1

      @@shreemoyde7031I think it has to do with how the electrons flow. If the nucleophile attacked and donated electrons to the alpha carbon, then the electrons from the carbon-carbon double bond would have to move onto the beta carbon, forming a carbanion. On the other hand, if the nucleophile attacked at the beta carbon, then the electrons can move up onto the oxygen, which is more electronegative.

    • @nostro1940
      @nostro1940 Před 8 měsíci +1

      has nothing to do with that otherwise why would a strong base work?@@PunmasterSTP

  • @chemist7908
    @chemist7908 Před 3 lety

    This was very informing, could you at some point do the thia-michael addition

  • @anubhabgoswami7188
    @anubhabgoswami7188 Před rokem

    I have a question
    suppose there is a leaving grp like a OME on the acceptor will 1,4 addition still be there or can the grp(OME) leave?

  • @gargitripathi6331
    @gargitripathi6331 Před 2 lety

    Thank you so much sir

  • @shanzasalam2630
    @shanzasalam2630 Před rokem

    Thank you Soo much sir 😢

  • @kashifarashidmalik6257

    Superb sir

  • @mekdesbelete8766
    @mekdesbelete8766 Před 3 lety

    my carbonyl lecture i love you

  • @samriddhimishra557
    @samriddhimishra557 Před 3 lety

    In the last ques won't the water also hydrolyse the cyanide to an acid I just got that part wrong...???

  • @5minchem563
    @5minchem563 Před 4 lety +2

    Very nice example of steric effects, which prevent the attack on carbonyl and favor michael addition’s product formation. Well done 👍🏻
    I also just made a video about Michael addition and would be happy to hear honest opinions :)

  • @intheworldoforganicchemist7384

    Please make a video about synthesis of vitamin A by darzen condensation and reformatsky condensation

  • @sumitsinha4199
    @sumitsinha4199 Před 4 lety

    Thanks sir

  • @adarshck3010
    @adarshck3010 Před 4 lety

    Thanks

  • @mediwise2474
    @mediwise2474 Před 3 měsíci

    Can acrylamide and acrylic acid undergoes micheal addition

  • @fabiocetrulo4462
    @fabiocetrulo4462 Před 2 lety

    Massive legend

  • @gaphenprojects4172
    @gaphenprojects4172 Před 3 lety

    Thanks Ganzalo

  • @lmaobuhbuh3563
    @lmaobuhbuh3563 Před 4 lety +2

    in the last step at 6:40 can I protonate the O- and then forms an enol and then the enol tautomerized into aldehyde ? (sr for bad english)

    • @aiswaryanath9844
      @aiswaryanath9844 Před 4 lety +2

      Enolates are resonance stabilized..so that step happen faster to stabilize it.
      More over keto form is more stable than enol,c=o is more stable bond than c=c.
      Hope it helped.

    • @aiswaryanath9844
      @aiswaryanath9844 Před 4 lety

      czcams.com/video/Egret-LpbTE/video.html
      A simplified chemistry channel.

    • @lmaobuhbuh3563
      @lmaobuhbuh3563 Před 4 lety

      @@aiswaryanath9844 thank you very much

  • @abouddrogo2504
    @abouddrogo2504 Před 4 lety

    Can you add mannich reaction plz

  • @kaviyarasanm7133
    @kaviyarasanm7133 Před rokem

    Sir how to calculate pka value?

  • @innocentntuli6995
    @innocentntuli6995 Před 6 lety +6

    Thank you sir you are a life saver.....can u plz do a face reveal please

    • @matthewellingsworth9238
      @matthewellingsworth9238 Před 4 lety

      Innocent Ntuli his voice reminds me of Mark Wahlberg... I think it’s Mark Wahlberg.

    • @MrXxColexX1
      @MrXxColexX1 Před 4 lety

      he'd probably make like 10k just by revealing his face.

    • @shatabdichanda636
      @shatabdichanda636 Před 4 lety

      @@matthewellingsworth9238 😂😂

  • @Inuhoozuki
    @Inuhoozuki Před 5 lety

    Whats the first prodcuts name o: ? Please and thank you

    • @timotheus34
      @timotheus34 Před 4 lety

      I think it is called 3-(1-oxoethyl)hexane-2,6-dione but I am not 100% sure if the =O at the last carbon atome is named as a ketone or an aldehyde

  • @user-pg3hw9qg8t
    @user-pg3hw9qg8t Před rokem

    Awesome

  • @teresafernando9509
    @teresafernando9509 Před 4 lety +2

    I believe you are missing a + on the nitrogen of nitroethane at 13:16

    • @yoselinelliott6744
      @yoselinelliott6744 Před 3 lety

      I was thinking the same thing! I was like do i know nothing about nitro group charges?

  • @akmikki3251
    @akmikki3251 Před 3 lety

    Isnt there a Internal tautomerization going on instead of just adding a hydrogen? czcams.com/video/dEdsR-6dKWE/video.html

  • @1.4142
    @1.4142 Před 2 lety

    If you're named michael you should apply to the michael acceptor school.

  • @pengpleb9523
    @pengpleb9523 Před 5 lety

    sup michael; patreeeeek

  • @nostro1940
    @nostro1940 Před 8 měsíci +1

    wants to explain the michael reaction... 1st we need a Michael donor
    *DOESNT EXPLAIN WHAT A MICHAEL DONOR IS*
    And people wonder why chemistry is hard... it's not hard but the teachers suck

  • @michelletheunambiguousslay93
    @michelletheunambiguousslay93 Před 8 měsíci +1

    Is this considered part of the Enolate/Enol/Keytone/Aldehyde reaction group? Have an exam in 5 days and looking for videos that help.