Chapter 17: Q27E (page 567)
Epoxides react with Grignard reagents to yield alcohols. Propose a mechanism.
Short Answer
The mechanism followed as:
Chapter 17: Q27E (page 567)
Epoxides react with Grignard reagents to yield alcohols. Propose a mechanism.
The mechanism followed as:
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(a)
(b)
(c)
p-Nitrophenol and 2,6-dimethyl-4-nitrophenol both have pKa 5 7.15, but 3,5-dimethyl-4-nitrophenol has pKa 5 8.25. Why is 3,5-dimethyl-4- nitrophenol so much less acidic?
How would you prepare the following compounds from 1-phenylethanol?
More than one step may be required.
(a) Acetophenone
(b) Benzyl alcohol
(c) m-Bromobenzoic acid
(d) 2-Phenyl-2-propanol
Propose a synthesis of bicyclohexylidene, starting from cyclohexanone as the only source of carbon.
As a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect to oxidize faster, cis-4-tert-butylcyclohexanol or trans-4-tert-butylcyclohexanol? Draw the more stable chair conformation of each molecule.
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