Skip to main content
Organic Chemistry
My Course
Learn
Exam Prep
AI Tutor
Study Guides
Textbook Solutions
Flashcards
Explore
Try the app
My Course
Learn
Exam Prep
AI Tutor
Study Guides
Textbook Solutions
Flashcards
Explore
Try the app
Back
21. Aldehydes and Ketones: Nucleophilic Addition - Part 5 of 7!
Download worksheet
Problem 1
Problem 2
Problem 3
Problem 4
Problem 5
Problem 6
Problem 7
Problem 8
Problem 9
Problem 10
Problem 11
Problem 12
21. Aldehydes and Ketones: Nucleophilic Addition - Part 5 of 7!
Download worksheet
Practice
Summary
Previous
2 of 12
Next
21. Aldehydes and Ketones: Nucleophilic Addition / Overview of Nucleophilic Addition of Solvents / Problem 2
Problem 2
Why might a chemist choose to use a secondary amine over a primary amine in a reaction with a carbonyl compound?
A
Secondary amines increase the yield of imine formation.
B
Secondary amines are less reactive, reducing side reactions.
C
To form an enamine which can be used in further reactions such as alkylation.
D
Primary amines always lead to undesirable imine formation.
AI tutor
0
0 Comments
Show Answer
More options