Complete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only). Step 1: keto form. Draw curved arrows. Select Draw Templates More C G H O : 0: Erase متبتى Q2 Q 11 Step 2: complete the structure, then add curved arrows. Select Draw Templates More 2 C H O H Erase Q2Q →
Complete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only). Step 1: keto form. Draw curved arrows. Select Draw Templates More C G H O : 0: Erase متبتى Q2 Q 11 Step 2: complete the structure, then add curved arrows. Select Draw Templates More 2 C H O H Erase 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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Please provide the mechanism!!
The tautomer that predominates in aqueous Solution? A. Enol form B. Keto form
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: keto form. Draw curved arrows.
Select Draw Templates More
/ ||||||
3
C
H
H
но
ö –
: 0
Erase
H
Q 2 2 Q
11
Step 2: complete the structure, then add
curved arrows.
Select Draw Templates More
/ //
JC
C H O
|
H-
: 0:
- н
K
Erase
Q2Q
I
Transcribed Image Text:Step 3: complete the structure, then add
curved arrows.
Select Draw Templates More
/ |||||| CH O
3
**
: 0
H-
-
0
: 0:
- Н
Erase
Q2 Q
11
step 4: enol form. Complete the structure.
Select Draw Templates More
/ ||| |||
3 C
C
H O
**
: 0–
Erase
H
Q2Q
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