(ii) Draw the product R, including a detailed reaction mechanism for the conjugate addition reaction between the 1,3-dicarbonyl P and the a,ß-unsaturated ketone Q. EtO P OEt Q OEt Et3N R (iv) Explain why conjugate addition is favoured over direct addition to Q in this case.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter24: Amines And Heterocycles
Section24.9: Heterocyclic Amines
Problem 24P
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(ii) Draw the product R, including a detailed reaction mechanism for the conjugate addition
reaction between the 1,3-dicarbonyl P and the a,ß-unsaturated ketone Q.
Eto
P
OEt
+
Q
OEt
Et3N
R
(iv) Explain why conjugate addition is favoured over direct addition to Q in this case.
Transcribed Image Text:(ii) Draw the product R, including a detailed reaction mechanism for the conjugate addition reaction between the 1,3-dicarbonyl P and the a,ß-unsaturated ketone Q. Eto P OEt + Q OEt Et3N R (iv) Explain why conjugate addition is favoured over direct addition to Q in this case.
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