Chapter 17: 8 P (page 539)
Question: What carbonyl compounds give the following alcohols on reduction with ? Show all possibilities.
(a)

(b)

(c)

(d)
Short Answer
(a)

(b)

(c)

(d)

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Chapter 17: 8 P (page 539)
Question: What carbonyl compounds give the following alcohols on reduction with ? Show all possibilities.
(a)

(b)

(c)

(d)
(a)

(b)

(c)

(d)

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Question:Identify the type of substitution mechanism ,involved in the conversion of the alcohol shown into the corresponding alkyl halide.
a.

b)

c)

Question: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)
Epoxides react with Grignard reagents to yield alcohols. Propose a mechanism.

The following data for isomeric four-carbon alcohols show that there is a decrease in boiling point with increasing substitution of the OH-bearing carbon. How might you account for this trend?
1-Butanol, bp
2-Butanol, bp
2-Methyl-2-propanol, bp
Reduction of 2-butanone with NaBH4yields 2-butanol. Is the product chiral? Is it optically active? Explain.
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