a. Epichlorohydrin reacts with dimethyl malonate to give an unusual product NaOMe Meo b. Ketals can be brominated under acidic conditions too! H*, Bra Br

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 7CTQ
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3
Provide a cdlear arrow-pushing mechanism for each of the following reactions. Do not skip proton
transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted
without ambiguity.
a. Epichlorohydrin reacts with dimethyl malonate to give an unusual product
NaOMe
MeO
b. Ketals can be brominated under acidic conditions too!
H*, Bra
Br
Transcribed Image Text:Provide a cdlear arrow-pushing mechanism for each of the following reactions. Do not skip proton transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted without ambiguity. a. Epichlorohydrin reacts with dimethyl malonate to give an unusual product NaOMe MeO b. Ketals can be brominated under acidic conditions too! H*, Bra Br
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