Each of the following alcohols has been subjected to acid-catalyzed dehydration and yields a mixture of two isomeric alkenes. Identify the two alkenes in each case, and predict which one is the major product on the basis of the Zaitsev rule.
(a)
(b)
(c)
Sample Solution (a) Dehydration of 2,3-dimethyl-2-butanol can lead to either 2,3- dimethyl-1-butene by removal of a C-1 hydrogen or to 2,3-dimethyl-2-butene by removal of a C-3 hydrogen
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The major product is 2,3-dimethyl-2-butene. It has a tetrasubstituted double bond and is more stable than 2,3-dimethyl-1-butene, which has a disubstituted double bond. The major alkene arises by loss of a hydrogen from the β carbon that has fewer attached hydrogens (C-3) rather than from the p carbon that has the greater number of hydrogens (C-1).
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