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Author Question: Identify the expected major product of the following reaction. ... (Read 39 times)

dbose

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on: Aug 23, 2018
Identify the expected major product of the following reaction.
 
 

Question 2

Which of the following explains why protons  to a carbonyl group show enhanced acidity?
  1.An inductive effect from the adjacent carbonyl weakens the C-H bond.
  2.The conjugate base is stabilized by resonance.
  3.The charge that results after deprotonation is delocalized.
  4.An inductive effect from the adjacent carbonyl weakens the C-H bond; and the conjugate base is stabilized by resonance.
  5.All of the answers


fwbard

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Reply #1 on: Aug 23, 2018
Answer to Question 1

3

Answer to Question 2

5


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