A mixture of 1-heptyne, 2-heptyne, and 3-heptyne was hydrogenated in the presence of a platinum catalyst until hydrogen uptake ceased. If one assumes that the hydrogenation went to completion, how many distinct seven-carbon hydrocarbons were produced?()
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Which of the following compounds will react most rapidly with HCl?()
A. 5-methyl-1-hexene
B. 4-methyl-1-hexene
C. E-5-methyl-2-hexene
D. E-2-methyl-3-hexene
E. 2-methyl-2-hexene
What is the major product from the acid-catalyzed hydration of 2-methyl-2-pentene? ()
A. 2-methylpentane
B. 2-methyl-1-pentanol
C. 2-methyl-2-pentanol
D. 2-methyl-3-pentanol
E. 1-methoxypentane
Identify the true statements in the mechanism in the addition of water to an alkene. ()
A. The addition of the electrophile is a slow step.
B. The addition of the nucleophile is a fast step.
C. A carbocation is formed as an intermediate.
D. Water abstracts the extra proton from the protonated alcohol.
E. All of the above
Give the product for the reaction of 1-butene with methanol in the presence of acid. The mechanism is the same as the mechanism for the addition of water to alkenes. ()
A. 1-ethoxybutane
B. 2-ethoxybutane
C. 1-methoxybutane
D. 2-methoxybutane
E. 1-butanol