Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter8: Addition Via Carbocation
Section: Chapter Questions
Problem 3E: Explain why ethene does not react with HX ( X=Cl , Br or I) under normal conditions.
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Question
Quinapril (trade name Accupril) is used to treat high blood pressure and congestive heart failure. One step in the synthesis of quinapril involves reaction of the racemic alkyl bromide A with a single enantiomer of the amino ester B. (a) What two products are formed in this reaction? (b) Given the structure of quinapril, which one of these two products is needed to synthesize the drug?
![H;N
HO.
Br
(CH3CH2}3N
quinapril
racemic A](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F92be639b-1f54-472d-bead-e8ab5553ff13%2F2b6ae698-de47-4312-97fd-113daf0c67c5%2Fg1vr73d.png&w=3840&q=75)
Transcribed Image Text:H;N
HO.
Br
(CH3CH2}3N
quinapril
racemic A
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