Chapter 16: Q9 P (page 495)
Question: Predict the major products of the following reactions:
(a) Nitration of bromobenzene
(b) Bromination of nitrobenzene
(c) Chlorination of phenol
(d) Bromination of aniline
Short Answer
a.
b.
c.
d.
Chapter 16: Q9 P (page 495)
Question: Predict the major products of the following reactions:
(a) Nitration of bromobenzene
(b) Bromination of nitrobenzene
(c) Chlorination of phenol
(d) Bromination of aniline
a.
b.
c.
d.
All the tools & learning materials you need for study success - in one app.
Get started for freePropose a mechanism for the reaction of 1-chloroanthraquinone with methoxide ion to give the substitution product 1-methoxyanthraquinone. Use curved arrows to show the electron flow in each step.
How would you synthesize the following compounds from benzene? Assume that ortho and para isomers can be separated.
The N,N,N-trimethylammonium group , is one of the few groups that is a meta-directing deactivator yet has no electron-withdrawing resonance effect. Explain
Propose a mechanism for the reaction of 1-chloroanthraquinone with methoxide ion to give the substitution product 1-methoxyanthraquinone. Use curved arrows to show the electron flow in each step.
Question: Phenols (ArOH) are relatively acidic, and the presence of a substituent group on the aromatic ring has a large effect. The of unsubstituted phenol, for example, is 9.89, while that of p-nitrophenol is 7.15. Draw resonance structures of the corresponding phenoxide anions and explain the data.
What do you think about this solution?
We value your feedback to improve our textbook solutions.