Answer both of the following questions precisely, succinctly, and with correct grammar. A. Explain in detail why sodium methoxide (NaOCH,) is more reactive than methanol (HOCH,) in S,2 reactions. Draw two analogous S,2 reactions, one for each reagent, to illustrate your answer.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
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Answer both of the following questions precisely, succinctly, and with correct grammar.
A. Explain in detail why sodium methoxide (NaOCH,) is more reactive than methanol (HOCH,)
in S,2 reactions. Draw two analogous S,2 reactions, one for each reagent, to illustrate your answer.
B. In principle, the conversion of an alkyl bromide into the corresponding alkene can be accomplished
either by an El or an E2 pathway. Explain in detail why the E2 mechanism usually is preferred.
Transcribed Image Text:Answer both of the following questions precisely, succinctly, and with correct grammar. A. Explain in detail why sodium methoxide (NaOCH,) is more reactive than methanol (HOCH,) in S,2 reactions. Draw two analogous S,2 reactions, one for each reagent, to illustrate your answer. B. In principle, the conversion of an alkyl bromide into the corresponding alkene can be accomplished either by an El or an E2 pathway. Explain in detail why the E2 mechanism usually is preferred.
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