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Electrophilic Aromatic Substitution

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Uploaded by on Oct 10, 2010

Electrophilic Aromatic Substitution

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LICENSE: Creative Commons (Attribution-Noncommercial-No Derivative Works).

For more information about this license, please read: http://creativecommons.org/licenses/by-nc-nd/3.0/.

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Top Comments

  • Thank you sooo much. You are going to help me pass my finals!

  • "It wants electrons really, really, really, really, REALLY bad!!" haha you are the man , thanks so much for this.

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All Comments (11)

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  • These video are amazing!!! Thank u so much from italy :)

  • like someone already said, UR THE MAN :]

  • I have watched all your videos. THEY ARE AWEEEEEEEEEEEEESOME. thank you.

    Do you have "Nitration of benzene mechanism"?

  • Why did the base go for the hydrogen instead of the carbocation?

  • Feel I may get lost in the sea of compliments, but Sal..once again you have succeeded in helping a very confused, mature, Open University Student to become a LOT less confumbled! Keeping doing what you do best, stimulating neurons without scaring them lol!

  • Oh my goodness!! Just what I need!!!

  • Great videos...thank you! What program/hardware are you using to draw/record?

  • If the electrophile is a halogen, the bond can be polarised by using a Lewis acid catalyst. If the electrphilic substitution is a sulphonation, then no Lewis acid is necessary, and the proton reacts with the sulphonate anion, forming the sulphonic acid.

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