Complete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only). Step 1: enol form Draw curved arrows. Select Draw Templates More / |||||| C : H : 0 0 <-H H Erase 11 Step 2: Draw curved arrows. Select Draw Templates More ✔ G C H O 0-H H : 0: Erase Q2 Q
Complete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only). Step 1: enol form Draw curved arrows. Select Draw Templates More / |||||| C : H : 0 0 <-H H Erase 11 Step 2: Draw curved arrows. Select Draw Templates More ✔ G C H O 0-H H : 0: Erase Q2 Q
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter16: Synthesis Workshop 1
Section: Chapter Questions
Problem 30CTQ
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provide the mechanism!
The tautomer that predominates in aqueous solution A. Enol B. Keto form
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