Halogenation of Alkenes & Halohydrin Formation Reaction Mechanism

[@TheOrganicChemistryTutor]

Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html Full-Length Exams and Worksheets: www.patreon.com/MathScienceTutor/collections Next Video: kzbin.info/www/bejne/gZnJcoOgoZusnpY Alkene Reactions: kzbin.info/www/bejne/ony1gItneJV9iNU

[@amacgregor92]

My professor rushed and spent like 2 minutes on this. Thank god I decided to check my understanding because there's way more to it than I thought.

[@PunmasterSTP]

I just came across your comment and was curious. How'd the class end up going?

[@xxllkira_editszx]

You guys study this in college or smth? :D

[@neroaintyourfriend]

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[@xxllkira_editszx]

@@neroaintyourfriend we have to study this in high-school :D

[@neroaintyourfriend]

That's impressive. it's just an extended course module, just for basics​@@xxllkira_editszx

[@exivir2010]

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[@deathwiddle3826]

Are you blamck???

[@ahorizontallychallengedora5262]

@@deathwiddle3826 👨🏿‍🌾

[@SaebaRyo21]

Thank you very much sir! You've explained an in-depth Halogenation of Alkenes in the presence of an inert solvent along with halohydrin formation with respective stereochemistry. I was searching such kind of single video, where all such useful concepts are present! Thank you! 😊

[@angelsdevil7521]

Lot of love from India 🇮🇳sir I totally understood this topic

[@proprofs8733]

Best explanation

[@DevSharma-ez1gx]

You explained wonderfully

[@jessicad7546]

Is it possible to monochlorinate an alkene, such as 1-pentene? The double bond is making it seem like monochlorination would not be possible, because then it would be dichlorination

[@aiyshasulaiman5755]

Very helpful. Thank you!

[@senny-]

i'm still confused by how both the bromine and the double bond attack each other. can someone explain?

[@hermanmangaba9547]

God bless you

[@RawDoggin_78]

i will name my son organic chemistry tutor

[@ekemulder9851]

What do you need the solvent for at 1:50? And how do you determine the solvent

[@schrodinger8605]

ch2cl2 is non polar solvent which helps in anti addition of bromine While h20 being polar substitutes oh and br

[@hananalsakka.330]

Thank you 😊

[@LifewithAmairanny]

beautiful

[@hainguyenthithanh7686]

0:48 why cyclohexen react with Br2 not form cacboncation and form cyclobromine ?

[@nickolauslim2068]

How do you determine where your OH group will end up? Do you just assume it will be on the wedge?

[@nolanschrader7230]

The h20 will attack the more substituted side of the bridged halonium, then is deprotonated by another H2O atom (in solution). You get trans enantiomers as products so the OH exists on the wedge in one conformation, and on the dash in another conformation. Same for the Br atom

[@alexw.1091]

no at all you study where there is a hydrogen atom .

[@moeburgol4863]

At 10:56, can we use Br (minus) instead of water to take off the hydrogen? Since we had Br2 in the beginning .

[@yourmummy13]

ye

[@tengwenxiang1692]

May i know why is the bromonium ion the positive on bromine? since i tot bromine is much more electronegative

[@magickitten742]

Sure love the "alkenes" here

[@anthonycobo21]

oh wait your second example is a meso compound so no enantomer

[@jaycarpentero3857]

what if two alkenes on the cyclohexane?

[@shahilali2555]

10:14 why didn't the Br- attak instead of H2O

[@kofiowusu8410]

Im not getting this one please help

[@marilynmegaro6506]

Are enantiomers always going to be a race mic mixture?

[@marilynmegaro6506]

Racemic *

[@PunmasterSTP]

Sometimes one enantiomer is produced more than the other, and sometimes only a single enantiomer is produced. I think the terms for those two situations are "stereoselective" and "stereospecific", respectively.

[@PunmasterSTP]

Halogenation of alkenes? More like "Hey, you've got amazing videos, know what I mean?" 👍

[@lauramarra6388]

Honestly still lost

[@yasc2723]

2:23 you mean E 2-butene?

[@RahmanIbraheem]

I get your point though but It’s the same thing. trans and E geometry are describing the same structure.

[@yasc2723]

@@RahmanIbraheem trans and cis are for cyclohexanes and E / Z are for alkenes.

[@RahmanIbraheem]

@@yasc2723 Okay, agreed. But I’m saying he’s not wrong with the naming of the compound.

[@kamalkishorebhuria8862]

Mechanism to bataya hi nhi

[@priyu8312]

Any indian?

[@Sweetener.-jy8ku]

We are everywhere bro

[@priyu8312]

@@Sweetener.-jy8ku Great

[@scottwerner5092]

Does anyone know this guy's name? a first name is fine, I just want to be able to refer to this guy without having to say "math and science tutor" or the "organic chemistry tutor"

[@fernandocruz9882]

Julio González

[@philipgao299]

is the benzene ring planar tho? so why would you have anti addition of the bromine?

[@jeremymcadams7743]

Benzene doesn't do dihalogenation. That was cyclohexene.