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 ||||||||| 3 Ć : 0 Step 3: complete the structure, then add curved arrows. Select Draw Templates More 3 Ć |||||| H ra Q2Q *2ª The tautomer that predominates in aqueous solution is the O keto form. enol form. Step 2: Draw curved arrows. Select Draw Templates More "M 3 Ć H 3 Ć H step 4: keto form. Complete the structure. Select Draw Templates Mar ||||||| CMO Era Q2Q Q2Q
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 ||||||||| 3 Ć : 0 Step 3: complete the structure, then add curved arrows. Select Draw Templates More 3 Ć |||||| H ra Q2Q *2ª The tautomer that predominates in aqueous solution is the O keto form. enol form. Step 2: Draw curved arrows. Select Draw Templates More "M 3 Ć H 3 Ć H step 4: keto form. Complete the structure. Select Draw Templates Mar ||||||| CMO Era Q2Q Q2Q
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter8: Addition Via Carbocation
Section: Chapter Questions
Problem 18CTQ: The reactants, intermediates, final products, and all curved arrows showing bonds forming...
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