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Electrophilic aromatic substitution (1)

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Uploaded by on Aug 1, 2009

Organic chemistry: Electrophilic aromatic substitution (EAS) of benzene—halogenation, nitration, sulfonation, Friedel-Crafts alkylation and alkanoylation. Electron-withdrawing and electron-donating groups—activators vs. deactivators, ortho/para-directors vs. meta-directors.

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(1) General mechanism for electrophilic aromatic substitution (EAS). Halogenation
(2) Continued. Nitration
(3) Sulfonation. Friedel-Crafts alkylation and alkanoylation
(4) Continued
(5) Activating vs. deactivating substituents
(6) Continued. Digression on nomenclature
(7) Activators and deactivators, continued
(8) Ortho/para-directors and meta-directors
(9) Continued
(10) Continued. Directing effects for disubstituted benzenes
(11) Continued
(12) Some aromaticity and Huckels rule problems


tags: educational college student education MCAT exam test

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  • When did Stephen Hawking get out of his wheelchair? relax, relax, just kidding.

  • Thanks to the girl also who asked you to show mechanism! She always asks good questions.

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  • I LOVE THIS VIDEO FOR REASONS!

  • This video is made of amazing.

  • THANKYOUUU for making me feel smart again!

  • i love your videos, but i still wish someone in germany would do something comparable... would be much easier^^

  • I wouldn't doubt that this man could be swimming in pussy as a write this. He knows everything.

  • @beverding u r right . he luks like Hawking

  • Omg you give me hope that I may pass o. chem ! THANKS BUDDY

  • whys the church holleriin hommie

  • cyclohexa-1,3,5- triene!

  • Lies, there is no C=C in Benzene it is a large singular delocalised π bond.

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