Why is the carboxylic acid proton (RCO2H) more downfield than the amide proton (RCONH)? Why do the alpha carbons of the carbonyls all have shifts further downfield?
Why is the carboxylic acid proton (RCO2H) more downfield than the amide proton (RCONH)? Why do the alpha carbons of the carbonyls all have shifts further downfield?
Chapter61: Friedel–crafts Acylation
Section: Chapter Questions
Problem 7Q
Related questions
Question
Why is the carboxylic acid proton (RCO2H) more downfield than the amide proton (RCONH)? Why do the alpha carbons of the carbonyls all have shifts further downfield?
Expert Solution
Step 1
Step by step
Solved in 2 steps with 1 images
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:
9781305446021
Author:
Lampman
Publisher:
CENGAGE LEARNING - CONSIGNMENT
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:
9781305446021
Author:
Lampman
Publisher:
CENGAGE LEARNING - CONSIGNMENT