Chapter 18: 6P (page 684)
What acid chloride would be needed to prepare each of the following ketones from benzene using a Friedel–Crafts acylation?
Chapter 18: 6P (page 684)
What acid chloride would be needed to prepare each of the following ketones from benzene using a Friedel–Crafts acylation?
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion: Ibufenac, a para-disubstituted arene with the structure HO2CCH2C6H4CH2CH(CH3)2, is a much more potent analgesic than aspirin, but it was never sold commercially because it caused liver toxicity in some clinical trials. Devise a synthesis of ibufenac from benzene and organic halides having fewer than five carbons.
Question: Draw a stepwise mechanism for the following intramolecular reaction, which is used in the synthesis of the female sex hormone estrone.
Consider the tetracyclic aromatic compound drawn below, with rings labeled as A, B, C, and D. (a) Which of the four rings is most reactive in electrophilic aromatic substitution? (b) Which of the four rings is least reactive in electrophilic aromatic substitution? (c) What are the major product(s) formed when this compound is treated with one equivalent of ?
Draw the products of each reaction
a)
b)
c)
What products are formed when benzene is treated with each alkyl chloride and ?
What do you think about this solution?
We value your feedback to improve our textbook solutions.