Chapter 17: 10 P (page 543)
Question: Use a Grignard reaction to prepare the following alcohols.
- 2-Methyl-2-propanol
- 1-Methylcyclohexanol
- 3-Methyl-3-pentanol
- 2-Phenyl-2-butanol
- Benzyl alcohol
- 4-Methyl-1-pentanol
Short Answer
(A)


(B)

(C)

(D)

(E)

(F)

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Chapter 17: 10 P (page 543)
Question: Use a Grignard reaction to prepare the following alcohols.
(A)


(B)

(C)

(D)

(E)

(F)

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Dehydration of trans-2-methylcyclopentanol with POCl3 in pyridine yields predominantly 3-methylcyclopentene. Is the stereochemistry of this dehydration syn or anti? Can you suggest a reason for formation of the observed product? (Make molecular models!)
What products would you expect from oxidation of the following compounds with in aqueous acid? With the Dess-Martin periodinane?
Identify the type of substitution mechanism involved in the conversion of the alcohol shown into the corresponding alkyl halide.
(a)

(b)

(c)

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
What Grignard reagent and what carbonyl compound might you startwith to prepare the following alcohols?
(a)
(b)
(c)
(d)
(e)
(f)
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