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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Compound A, , has the IR and NMR spectra shown. Proposea structure consistent with the observed spectra, and label each peak inthe NMR spectrum. Note that the absorption at disappears when is added.

Assume that you need to prepare 5-Cholesten-3-one from Cholesterol. How could you use IR spectroscopy to tell whether the reaction was successful? What differences would you look for in the IR spectra of starting material and product?

Show the mechanism for the reaction of p-methylphenol with 2-methylpropene and catalyst to yield the food additive BHT.
The reduction of carbonyl compounds by reaction with hydride reagents and the Grignard addition by reaction with organomagnesium halides are examples of nucleophilic carbonyl addition reactions. What analogous product do you think might result from reaction of cyanide ion with a ketone?

Question: How would you prepare the following compounds from
2-phenylethanol?
More than one step may be required.
(a) Styrene
(b) Phenylacetaldehyde
(c) Phenylacetic acid
(d) Benzoic acid
(e) Ethylbenzene
(f) Benzaldehyde
(g) 1-Phenylethanol
(h) 1-Bromo-2-phenylethane
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