Mixed Crossed Aldol Reaction Trick and Limiting Products

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  • Опубликовано: 5 окт 2024
  • leah4sci.com/en... presents: Mixed or Cross Aldol Condensation using Aldehydes and Ketones for mixed products
    Need help with orgo? Download my free guide '10 Secrets to Acing Organic Chemistry' HERE: leah4sci.com/or...
    This video shows you how to identify all products in a mixed or cross aldol reaction including how to limit side products
    This is video 6 in the Enolate Reaction series. Catch the entire series along with the Enolate practice quiz and cheat sheet on my website: leah4sci.com/en...
    For more in-depth review including practice problems and explanations, check out my online membership site: studyhall.leah4...
    For private online tutoring visit my website: leah4sci.com/or...
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Комментарии • 50

  • @tiibrahim5714
    @tiibrahim5714 6 лет назад +33

    Seriously this is magic you cover two hours lectures within 11 minutes.thanks a lot

    • @Leah4sci
      @Leah4sci  6 лет назад +2

      Too funny about it being magic! You're very welcome :)

  • @nSackStyles
    @nSackStyles 7 лет назад +25

    This seriously cannot be a 11 min video. It cannot. Is it? really? There's a mistake i guess!
    I mean thanks a lot LEAH, you cover so much theory in a video which looks so small.
    Every sentence you speak, has an important note and a deep theory inside. You edit it, so that we can skip to the most important parts. That is the reason, why it covers an entire lecture in 11 min video. THANK YOU!

    • @Leah4sci
      @Leah4sci  9 месяцев назад

      Oh wow, thanks so much for all of your kind words, I'm beyond happy to help

  • @princessogwu2939
    @princessogwu2939 Год назад +2

    May God bless you, Leah. I thought for sure I was going to fail this topic. You made it easy to understand, and your examples were comprehensive.

    • @Leah4sci
      @Leah4sci  Год назад

      Always happy to help! Thanks for watching. :)

  • @anagar4434
    @anagar4434 7 лет назад +8

    really like how you explain everything so easy!!☺

    • @Leah4sci
      @Leah4sci  7 лет назад +1

      Glad you enjoyed it!

  • @siyandadube8352
    @siyandadube8352 Год назад +1

    Wow this is beautiful, you just made it simple and straight forward. SIMPLICITY

  • @EmelithCErbito99
    @EmelithCErbito99 8 лет назад +4

    you saved my life .. ur techniques are amazing ! I love your videos ! my exam is coming up

    • @Leah4sci
      @Leah4sci  9 месяцев назад

      Yay, so happy to help!

  • @razlemaze29876
    @razlemaze29876 4 года назад +2

    thank you so much. ive been struggling to get this down

  • @gevorgdanielyan1685
    @gevorgdanielyan1685 6 лет назад +3

    Very helpful and right to the point.

    • @Leah4sci
      @Leah4sci  5 лет назад

      Glad the video helped! Thanks!

  • @shashwatdogra9786
    @shashwatdogra9786 4 года назад

    your videos are far batter than coaching classes for engineering ug entrance in India thanks mam

    • @Leah4sci
      @Leah4sci  4 года назад +1

      It's my pleasure!

  • @redibeyan8777
    @redibeyan8777 6 лет назад +1

    Really awesome video​ !!

  • @DrMohammedHashimAL-Thahbi
    @DrMohammedHashimAL-Thahbi 8 лет назад

    Thank you very much Dr.Leah Fisch

    • @Leah4sci
      @Leah4sci  8 месяцев назад

      Not a Dr, but you're very welcome :)

  • @jessicajohnson1180
    @jessicajohnson1180 6 месяцев назад

    This was great, thank you!!!!

    • @Leah4sci
      @Leah4sci  6 месяцев назад

      You're so very welcome!

  • @apoorvtyagi7441
    @apoorvtyagi7441 6 лет назад +1

    Thanks ma'am. This video was very helpful. But is there anyway we can tell which product is going to be major or are they just formed in equal proportional if we take equal moles if reactants?

    • @Leah4sci
      @Leah4sci  6 лет назад

      Glad you found the video helpful, but I'm sorry. I don't offer tutoring over RUclips comments. For more help with this, I recommend joining the orgo study hall. Full details: leah4sci.com/join

  • @youssefatef5633
    @youssefatef5633 3 года назад

    Iam form Egypt Finally I understoooooooood I will tell you thanks in Arabic [شكرا]

    • @Leah4sci
      @Leah4sci  3 года назад

      Yay, glad you understand now!

  • @leularegawi1735
    @leularegawi1735 3 месяца назад

    Thank you so much, you're the best fr😊

    • @Leah4sci
      @Leah4sci  3 месяца назад

      Aww you're very welcome!

  • @nimoosman7716
    @nimoosman7716 7 месяцев назад

    Thank you madam i understood ❤

    • @Leah4sci
      @Leah4sci  7 месяцев назад

      You're welcome!

  • @keerthanasatheesh9639
    @keerthanasatheesh9639 3 года назад +1

    OMGOD T?HIS TICK IS SOOO GOOD

    • @Leah4sci
      @Leah4sci  3 года назад +1

      Glad you like it!

  • @mohamadhanan5706
    @mohamadhanan5706 3 года назад +1

    See you in haven, Leah

  • @sarahbahreinian9713
    @sarahbahreinian9713 3 года назад

    @leah4sci or anyone who can help! When you have a ketone, how do you tell what "#2" is? How can you tell which carbon is the alpha carbon?
    Is it the presence of a hydrogen atom that is needed? Also, whichever "R" group on the ketone that is less sterically hindered will be preferred?

    • @Leah4sci
      @Leah4sci  2 года назад

      The alpha carbon is the one adjacent to the carbon of the carbonyl group. I'm unsure of exactly what you're asking in regards to R groups. Less bulky R groups will facilitate the reaction due to steric effects.

  • @brendamanni9087
    @brendamanni9087 6 лет назад

    I don't know when you number the ketone first or the aldehyde first in the reaction how do you tell? That is the only thing I get wrong. Thank you.

    • @Leah4sci
      @Leah4sci  5 лет назад

      At which part of the video?

  • @PunmasterSTP
    @PunmasterSTP 2 года назад

    Crossed aldol reaction trick? More like "Cool videos, and your presentation style is slick!" 👍

  • @watertantrums2000
    @watertantrums2000 2 года назад

    Please at 3:42 why is there a methyl on carbon 3?
    Ok I see a pattern...when there is no H attached(ketone) there's an extra methyl added in the product, I hope I am right.

    • @Leah4sci
      @Leah4sci  2 года назад

      Yes, I think you have it. The methyl on carbon 3 was the same methyl group in the original ketone, that was opposite the phenyl group. Each molecule reacting brought two carbons that were outside of the benzene ring.

    • @watertantrums2000
      @watertantrums2000 2 года назад

      @@Leah4sci thank you

  • @rahulmathias8758
    @rahulmathias8758 7 лет назад

    How do we do it with benzaldeyhyde and 1 phenyl Ethanone

    • @Leah4sci
      @Leah4sci  7 лет назад

      I'm sorry, but I don't offer tutoring through RUclips comments. For help with questions like this and more, I recommend you join the organic chemistry study hall. Details: leah4sci.com/join

  • @shnoalimhamadkaram1594
    @shnoalimhamadkaram1594 Год назад

    hellow teacher
    if we have (acetone + 2,2-di methy propanal ) also we have 4 product ?

    • @Leah4sci
      @Leah4sci  Год назад +1

      I'm sorry, but I don't offer tutoring over social media. For help with questions like this and more, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/

    • @shnoalimhamadkaram1594
      @shnoalimhamadkaram1594 Год назад

      Thanks a lot dear teacher .