Consider the three organic compounds shown, and then select the options that currently describe how you would evaluate their relative acidity. A B Choose one or more: Compound A is the least stable acid because of the CH3 group. Compounds B and C have similar stability because they both contain N. The conjugate base of A is resonance-stabilized. Compound B is the least stable acid because of the charge on N. The conjugate base of A is stabilized by induction. The conjugate base of C is stabilized by induction.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter20: Acidity And Pka Of Phenols
Section: Chapter Questions
Problem 9E
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Consider the three organic compounds shown, and then select the options that currently
describe how you would evaluate their relative acidity.
A
B
Choose one or more:
Compound A is the least stable acid because of the CH3 group.
Compounds B and C have similar stability because they both contain N.
The conjugate base of A is resonance-stabilized.
Compound B is the least stable acid because of the charge on N.
The conjugate base of A is stabilized by induction.
The conjugate base of C is stabilized by induction.
Transcribed Image Text:Consider the three organic compounds shown, and then select the options that currently describe how you would evaluate their relative acidity. A B Choose one or more: Compound A is the least stable acid because of the CH3 group. Compounds B and C have similar stability because they both contain N. The conjugate base of A is resonance-stabilized. Compound B is the least stable acid because of the charge on N. The conjugate base of A is stabilized by induction. The conjugate base of C is stabilized by induction.
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