[Skip Breadcrumb Navigation]
:
[Skip Breadcrumb Navigation]
Home
Chapter 13: Carbonyl Compounds III: Reactions at the α-Carbon
Exercises
Practice Exercise 2
Practice Exercise 2
This activity contains 5 questions.
What would be the product of the malonic ester synthesis if methyl bromide were used as the alkyl halide?
methanoic acid
propanone
methyl acetate
methyl malonate
propanoic acid
Which pair of compounds would form the greatest yield of a single product in a mixed aldol addition?
formaldehyde and benzaldehyde
acetone and propiophenone
acetone and acetaldehyde
acetone and benzaldehyde
acetone and propanone
What product is formed when malonic acid is heated?
formic acid
formaldehyde
acetic acid
propanoic acid
acetaldehyde
What product is formed when 1-bromobutane is used in an acetoacetic ester synthesis?
CH
3
CH
2
-C(=O)-CH
3
CH
3
CH
2
CH
2
CH
2
-C(=O)-CH
3
CH
3
CH
2
CH
2
CH
2
CH
2
-C(=O)-CH
3
CH
3
CH
2
CH
2
-C(=O)-CH
3
CH
3
CH
2
CH
2
CH
2
-CH=O
Which of the following carbonyl compounds would give the largest amount of enol when dissolved in water?
2,5-hexanedione
2,4-hexanedione
3,4-hexanedione
3-hexanone
hexanal
The Clear Answers feature requires scripting to function. Your browser either does not support scripting or you have turned scripting off. So, the Clear Answers feature will not work. Note that you do not need to use the Clear Answers feature in order to use this site. You can change your answers for each question individually.
Your browser either does not support scripting or you have turned scripting off. Because of this, the answer choices will NOT appear in a different order each time the page is loaded, though that is mentioned below. Note that you do not need this feature to use this site.
Answer choices in this exercise appear in a different order each time the page
is loaded.
Copyright © 1995 - 2021
Pearson Education
. All rights reserved. Pearson Prentice Hall is an imprint of
Pearson
.
Legal Notice
|
Privacy Policy
|
Permissions
[Return to the Top of this Page]
: return
