PROBLEM 25.13
Question
Question: Draw the product of each reaction.
a.
b.
c.
d.
Step-by-Step Solution
Verified Answer
Answer
a.
b.
c.
d.
1Reduction of aldehyde to imine
The aldehyde is reduced to imine when the amine attacks the carbonyl carbon. The lone pair of electrons moves from the amine group to the electron-deficient group of C=O.
2Reduction of imine to amine
The reduction of imine to amine is completed in the presence of reducing agents, such as lithium aluminum hydride, sodium cyanoborohydride, etc. The reducing agents produce hydride in the deficient groups.
3Explanation
a. The given aldehyde compound is reduced to amine, as shown below.
Reduction of aldehyde
b. The given ketone compound is reduced to amine, as shown below.
Reduction of aldehyde
c.
Reduction of aldehyde
d. The given ketone compound is reduced to amine, as shown below.
Reduction of aldehyde
Other exercises in this chapter
PROBLEM 25.11
What amine is formed by reduction of each amide?a.b.c.
View solution PROBLEM 25.12
Which amines cannot be prepared by reduction of an amide?a.b.c.d.
View solution PROBLEM 25.14
Question: Enalapril, a drug used to treat hypertension, is prepared from compounds D and E by reductive amination. What is the structure of enalapril?
View solution PROBLEM 25.16
Question: a. Explain why phentermine phCH2CCH32NH2 can't be made by a reductive amination reaction. b. Give a systematic name for phentermine, one of
View solution