omplete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved rows (forward reaction only). Do not remove any pre-drawn bonds or lone pairs. step 1: enol form. Add curved arrows. Select Draw Templates More 3 Ĉ Step 3: complete the structure, then add curved arrows. 020 Select Draw Templates More H: • 026 The tautomer that predominates in aqueous solution is the Oenol form. keto form. Step 2: complete the structure, then add curved arrows. Select Draw Templates More 4101 ! H Step 4: complete the keto form Select Draw Templates Mar Ć apa "I CM D: Qa
omplete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved rows (forward reaction only). Do not remove any pre-drawn bonds or lone pairs. step 1: enol form. Add curved arrows. Select Draw Templates More 3 Ĉ Step 3: complete the structure, then add curved arrows. 020 Select Draw Templates More H: • 026 The tautomer that predominates in aqueous solution is the Oenol form. keto form. Step 2: complete the structure, then add curved arrows. Select Draw Templates More 4101 ! H Step 4: complete the keto form Select Draw Templates Mar Ć apa "I CM D: Qa
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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