Chapter 18: Q 51. (page 723)
Question: Using resonance structures, explain why a nitroso group (-NO) is an ortho, para director that deactivates a benzene ring toward electrophilic attack.
Short Answer
Answer
Chapter 18: Q 51. (page 723)
Question: Using resonance structures, explain why a nitroso group (-NO) is an ortho, para director that deactivates a benzene ring toward electrophilic attack.
Answer
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.
Rank the following compounds in order of increasing reactivity in electrophilic aromatic substitution.
What product is formed when benzene is treated with each organic halide in the presence of .
What acid chloride would be needed to prepare each of the following ketones from benzene using a FriedelโCrafts acylation?
Question: Explain the reactivity and orientation effects observed in each heterocycle.
a. Pyridine is less reactive than benzene in electrophilic aromatic substitution and yields 3-substituted products.
b. Pyrrole is more reactive than benzene in electrophilic aromatic substitution and yields 2-substituted products.
What do you think about this solution?
We value your feedback to improve our textbook solutions.