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Answer to Question #42215 in Organic Chemistry for Matthew Burke
Question #42215
Clearly illustrate, using curved arrows, each step of mechanism of the following:
i. reaction of an acetylide anion with bromomethane.
ii. reaction of 2-methylpropene with HBr (ionic mechanism).
iii. reaction of chloroethane with sodium ethoxide (elimination reaction).
i. reaction of an acetylide anion with bromomethane.
ii. reaction of 2-methylpropene with HBr (ionic mechanism).
iii. reaction of chloroethane with sodium ethoxide (elimination reaction).
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