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Favored reaction (circle one): SN2 or E2 H3C CH3 Br NaOCH3 CH3 23 °C CH3

Favored reaction (circle one): SN2 or E2 H3C CH3 Br NaOCH3 CH3 23 °C CH3

Organic Chemistry
Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 53AP
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circle the favored reaction and draw the major product. If the product has stereocenter(s), include stereochemistry, drawing the major configurational isomer formed. Assume the reactions are irreversible. Make sure the correct atoms of substituents are attached to the rest of the molecule. E.g., for NaCN, which atom of –CN is nucleophilic? It might be helpful to number carbons.

Favored reaction (circle one): SN2 or E2 H3C CH3 Br NaOCH3 CH3 23 °C CH3
Transcribed Image Text:Favored reaction (circle one): SN2 or E2 H3C CH3 Br NaOCH3 CH3 23 °C CH3
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