Friedel Crafts Acylation of Benzene Reaction Mechanism

[@TheOrganicChemistryTutor]

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[@Benzenediol]

I’ve been watching your content for a while now and I must say that I am very happy! We study this stuff in high school (we do advanced chemistry) and not only it made me better at the subject but it also made me somewhat love it. Honestly my chemistry teacher does a horrible job when it comes to motivating students, our work is never good enough for her, she makes students hate the subject and she expects way too much from us when we have pretty much just started our journey with this professional chemistry. I recall hating chemistry for the longest time. But this very content made me like it.

[@satvikaputcha]

That was very helpful!! Thanks!!

[@shashankchowdhary1784]

I think we have to take alcl3 anhydrous. h2o should not be taken as alcl3 will form coordinate bond with oxygen in h2o rather than cl.

[@tom_winguill]

1:02 is that benzene or a cyclo hexane

[@WSashy]

It's benzene because he drew the electrons inside the ring (they were blue, maybe a bit difficult to recognize)

[@pragnamamidipaka6154]

Hey! Catalytic hydrogenation of ketones gives alcohols right!

[@reenanwa]

are the reduction methods interchangeable? can i pick and choose?

[@Kelly-pf6hz]

Thanks now i can make my favourite cathinones :)

[@collinsm1687]

Blessings to you

[@wijdanayoub9770]

6:08 How could there still Alcl3 in the solution while it turned into Alcl4 - and reacted with the hydrogen came from benzene previously??

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never gonna give u up !!

[@edithkanja8002]

Thank you lot,God bless you

[@aliisleem4262]

What name of book you are using?

[@azyle2104]

Probably used many diff books and combined methods and stuff to teach it in his own way

[@khashayarsarmadi1433]

How does catalyzed hydrogenation (H2/Pd) remove the ketone-oxygen?

[@jesusmrosario-claudio4104]

Thank you once again.

[@nandianandia8702]

thanks for helping me

[@carlyjaff1935]

this was very helpful thank you

[@muminahmadbhat2658]

Love ur methods

[@m_jai3728]

i think you should start representing the bezene with the circle in the middle rather than the kekule structure since it causes confusion

[@proclubsgang8766]

Harder to show intermediates

[@LoneWolf-nt8up]

Then how you do show resonance 😂?

[@OgechukwuFlorence-uj7kx]

This was helpful

[@Darkshd]

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[@AmruMagdy]

Thanks 😊🙏❤

[@atlantascholar9572]

It would be better to start with a tertiary alkyl halide so a tertiary carbocation will be induced which is much more stable?

[@nursyahirahsuhaili5527]

hi anyone know why In the experiment synthesis of 4-bromobenzophenone excess of benzoyl chloride and aluminium chloride were used to react with bromobenzene ?

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Thank you Sir.

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I did. Here it is: www.patreon.com/MathScienceTutor

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[@Trident_Gaming03]

My professor is actually incompetent

[@aravindhkumar3976]

Isn't positive charge on a sp2 carbon unstable and doesn't form?

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[@LopamudraMohapatra-o9t]

You didn't made benzene in the first reaction