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

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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