235L-1. Write a mechanism to explain the formation of the 1,2-dioxetanedione intermediate upon treating divanillyl oxalate with hydrogen peroxide and sodium hydroxide (Scheme 4). Hint: Both of the singly-bonded oxygen atoms in the 1,2-dioxetanedione are derived from hydrogen peroxide.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
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Problem 34MP: Amino acids can be prepared by reaction of alkyl halides with diethyl acetamidomalonate, followed by...
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235L-1.
Write a mechanism to explain the formation of the 1,2-dioxetanedione
intermediate upon treating divanillyl oxalate with hydrogen peroxide and sodium hydroxide
(Scheme 4). Hint: Both of the singly-bonded oxygen atoms in the 1,2-dioxetanedione are derived
from hydrogen peroxide.
Transcribed Image Text:235L-1. Write a mechanism to explain the formation of the 1,2-dioxetanedione intermediate upon treating divanillyl oxalate with hydrogen peroxide and sodium hydroxide (Scheme 4). Hint: Both of the singly-bonded oxygen atoms in the 1,2-dioxetanedione are derived from hydrogen peroxide.
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