Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products indicate major product or if products are formed in equal amounts. If there is no reaction expected explain why.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...
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My question is really focused on the 2nd step - I recognize this is following a Kiliani Fischer Synthesis but will the final product included the Me from the MeOH

Provide the structure of the product(s) with stereochemisty if appropriate.
If multiple products indicate major product or if products are formed in
equal amounts. If there is no reaction expected explain why.
CHO
NaCN
i) Ba(OH)2
ii) MeOH, H₂SO4
H-
HO
H
OH
-H
-OH
CH₂OH
Transcribed Image Text:Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products indicate major product or if products are formed in equal amounts. If there is no reaction expected explain why. CHO NaCN i) Ba(OH)2 ii) MeOH, H₂SO4 H- HO H OH -H -OH CH₂OH
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