E1 Elimination: mechanism

More free lessons at: www.khanacademy.org/video?v=28...

Пікірлер: 31

  • @WhiteKillerRabbits
    @WhiteKillerRabbits11 жыл бұрын

    Dude....oh my gosh. WHY DON'T MORE PEOPLE KNOW ABOUT THIS?! I've been looking for videos that explain the idea of E1 Elimination mechanisms fully and clearly, and I haven't been able to find one. Until now. Thank you, SO much.

  • @unitelanka
    @unitelanka9 жыл бұрын

    great video. you get really worked up to some excitement towards the end :)

  • @rawandgot6134
    @rawandgot61347 жыл бұрын

    why does the water attacks the proton i mean isn't the sulfuric acid more reactive i mean it needs to have 8 electrons HSO4- which now has 7 ?

  • @username6333
    @username633311 жыл бұрын

    Excellent video.

  • @OrgoMadeEasy
    @OrgoMadeEasy11 жыл бұрын

    Great video on the mechanisms! I'm actually trying to do something similar on my channel with Orgo hopefully I'll be able to explain it just as well as you :D

  • @balletto14
    @balletto149 жыл бұрын

    If o chem has taught me anything, it's how to draw perfect hexagons and seeing yours were like nails on a chalk board but other than that this video is amazing

  • @Bripirate
    @Bripirate6 жыл бұрын

    Why wouldn't the bromide anion grab the proton rather than the ethanol?

  • @lyricson4ya

    @lyricson4ya

    3 жыл бұрын

    Because bromide is a weak base and hence is more stable as bromide ion....ethanol being a stronger base will accept the proton

  • @MrOmar4159
    @MrOmar41599 жыл бұрын

    thanks man, helped a lot

  • @shotdoctor5869
    @shotdoctor58698 жыл бұрын

    Why would ethanol act as a base and not a nuecleophile for Sn1 reaction? That doesn't make sense to me. It's not a good base.

  • @BryhanEspinosa

    @BryhanEspinosa

    8 жыл бұрын

    +TheShot Doctorr No it's possible. It's called competitive reactions. An E1 elimination reaction and Sn1 reaction compete for the reactants. So it is possible for the ethanol to attack the carbocation intermediate .

  • @Bripirate

    @Bripirate

    6 жыл бұрын

    I think the SN1 is not favored because of the heat involved. I think I recall heat having a big influence on SN1 or E1.

  • @deefaaabulous9081
    @deefaaabulous90819 жыл бұрын

    Where do the H+ protons come from? From the H2SO4?

  • @geekbuddy4

    @geekbuddy4

    9 жыл бұрын

    DeeFaaabulous Yes. From the H2SO4. Sulphuric acid in it's aqueous state dissociates into two protons (H+) and one SO4(2-) ion.

  • @maryamasad8830

    @maryamasad8830

    6 жыл бұрын

    DeeFaaabulous yes

  • @alethfideli5087
    @alethfideli50878 жыл бұрын

    Chemistry is a very broad subject in Science

  • @Geeskaihin
    @Geeskaihin4 жыл бұрын

    thanks for yoour charming suggetion

  • @karmoosh100
    @karmoosh10011 жыл бұрын

    Thank you :)

  • @anujgiri5793
    @anujgiri57939 жыл бұрын

    how Oxygen gets positive charge. and what about those remaining lone pairs??

  • @BryhanEspinosa

    @BryhanEspinosa

    8 жыл бұрын

    +anuj giri Oxygen has a positive charge because it has 3 bonds and one lone pair. So it has 5 electrons in total and a neutral oxygen has 6 electrons! Hope this helped. I don't know what you mean by the remaining lone pairs. If you're asking why there's a lone pair and not one electron is because electrons like to have complete orbitals. That's why you will never have a single electron, although in Quantum mechanics that can be refuted but that's a different story.

  • @gehad-alsanwee.
    @gehad-alsanwee.11 жыл бұрын

    Thank you so much

  • @itachi2011100
    @itachi20111009 жыл бұрын

    @ 10:54 two beta carbons were labeled while there were three of them

  • @BryhanEspinosa

    @BryhanEspinosa

    8 жыл бұрын

    +Harsh Parekh No, there's only two beta carbons. The carbon you're referring to is the Alpha carbon. Why? Because that carbon is directly bonded to the leaving group. However alpha carbons can undergo a reaction known as a Sn1 reaction where the ethanol will act as nucleophile rather than a base.

  • @itachi2011100

    @itachi2011100

    8 жыл бұрын

    +Bryhan Espinosa I am talking about the carbon in methyl group

  • @BryhanEspinosa

    @BryhanEspinosa

    8 жыл бұрын

    Harsh Parekh Oh yes, you are correct.

  • @BryhanEspinosa

    @BryhanEspinosa

    8 жыл бұрын

    Harsh Parekh Also, what I meant to say was that a Sn1 reaction can occur on the tertiary carbon as well.

  • @toomuchcandor3293

    @toomuchcandor3293

    8 жыл бұрын

    +Harsh Parekh You should totally report these bastards

  • @user-be4yc2vr5c
    @user-be4yc2vr5c4 жыл бұрын

    Ok so clearly sorting by upload date only worked for the first 6 videos. Where am I supposed to go now? Because this I understand= zero. I must have missed a ton somewhere? Ya'll need better playlists on this. With the recommended viewing order for learning this stuff. Like throwing 80 books of french with all varying degrees and someone and saying hop in and learn french. Not to sound ungrateful, thank you for the vids. Just as stands now they pretty useless till organized in order. =/