Chapter 17: Q45E (page 567)
How would you synthesize the following alcohols, starting with benzene and other alcohols of six or fewer carbons as your only organic reagents?
(a)
(b)
(c)
(d)
Short Answer
(a)
(b)
(c)
(d)
Chapter 17: Q45E (page 567)
How would you synthesize the following alcohols, starting with benzene and other alcohols of six or fewer carbons as your only organic reagents?
(a)
(b)
(c)
(d)
(a)
(b)
(c)
(d)
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Get started for freePropose a synthesis of bicyclohexylidene, starting from cyclohexanone as the only source of carbon.
Starting from testosterone (Problem 17-62), how would you prepare the following substances?
a.
b.
c.
d.
TMS ethers can be removed by treatment with fluoride ion as well as by acid-catalyzed hydrolysis. Propose a mechanism for the reaction of cyclohexyl TMS ether with LiF. Fluorotrimethylsilane is a product.
Benzyl chloride can be converted intobenzaldehyde by treatment with nitromethane and base. The reactioninvolves the initial conversion of nitromethane in to its anion, followed by SN2 reaction of the anion with benzyl chloride and subsequent E2 reaction. Write the mechanism in detail, using curved arrows to indicate the electron flow in each step.
Benzyl chloride Nitromethane anion Benzaldehyde
The trimethylsilyl (TMS) protecting group is one of several silicon protecting groups for alcohols. For each reaction, draw the mechanism for the protection of (R)-3-bromo-1-butanol with the following silyl chlorides, using triethylamine as the base:
(a) tert-butyldimethylsilyl chloride (TBS-Cl)
(b) triisopropylsilyl chloride (TIPS-Cl)
(c) triethylsilyl chloride (TES-Cl)
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