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
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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provide the mechanism!
The tautomer that predominates in aqueous solution A. Enol B. Keto form

Transcribed Image Text:Step 3: complete the structure, then add
curved arrows.
Select Draw Templates More
/ |||||| C H O
C
-:- -H
H-O
0:
Erase
✪ 2 Q
11
step 4: keto form. Complete the structure.
Select Draw Templates More
/ |||||| C HO
:
: 0:
- Н
Erase
Q2Q

Transcribed Image Text: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
CHO
C
..
: о — н
: 0 -H
Erase
2 Q
11
Step 2: Draw curved arrows.
Select Draw Templates More
/ ||| ||| C
S C
: 0
|
H
Н
HO
- H
Q
Erase
2 Q
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