Chapter 16: Q64E (page 524)
How would you synthesize the following substances starting frombenzene?
(a)
(b)
(c)
Short Answer
(a)
Synthesis of compound (a)
(b)
Synthesis of compound (b)
(c)
Synthesis of compound (c)
Chapter 16: Q64E (page 524)
How would you synthesize the following substances starting frombenzene?
(a)
(b)
(c)
(a)
Synthesis of compound (a)
(b)
Synthesis of compound (b)
(c)
Synthesis of compound (c)
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Get started for freeWould you expect p-methylphenol to be more acidic or less acidic than unsubstituted phenol? Explain. (See Problem 16-75.)
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.
Rank the compounds in each group according to their reactivity toward electrophilic substitution.
The carbocation electrophile in a Friedel–Crafts reaction can be generated by an alternate means than reaction of an alkyl chloride with. For example, reaction of benzene with 2-methylpropene in the presence of yields tert-butylbenzene. Propose a mechanism for this reaction.
What aromatic products would you obtain from the oxidation of the following substances?
a.
b.
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