Friedel Crafts Acylation of Benzene Reaction Mechanism
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- Опубликовано: 6 май 2018
- This organic chemistry video tutorial provides a basic introduction into the friedel crafts acylation reaction mechanism of benzene. It explains how to add a ketone functional group to a benzene ring using an acid chloride and an AlCl3 lewis acid catalyst. In addition, it explains how to reduce the ketone into an alkyl group using the clemmensen reduction reaction.
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That was very helpful!! Thanks!!
Love ur methods
this was very helpful thank you
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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.
Thanks now i can make my favourite cathinones :)
Thank you Sir.
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This was helpful
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are the reduction methods interchangeable? can i pick and choose?
Lovely
How does catalyzed hydrogenation (H2/Pd) remove the ketone-oxygen?
Hey! Catalytic hydrogenation of ketones gives alcohols right!
It would be better to start with a tertiary alkyl halide so a tertiary carbocation will be induced which is much more stable?
1:02 is that benzene or a cyclo hexane
It's benzene because he drew the electrons inside the ring (they were blue, maybe a bit difficult to recognize)
What name of book you are using?
Probably used many diff books and combined methods and stuff to teach it in his own way
hi anyone know why In the experiment synthesis of 4-bromobenzophenone excess of benzoyl chloride and aluminium chloride were used to react with bromobenzene ?
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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i think you should start representing the bezene with the circle in the middle rather than the kekule structure since it causes confusion
Harder to show intermediates
Then how you do show resonance 😂?
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Isn't positive charge on a sp2 carbon unstable and doesn't form?
wolf-kishna-黄鸣龙
You didn't made benzene in the first reaction
My professor is actually incompetent