Which of the following alkyl bromide isomers would most readily undergo an Sn2 reaction?
Understand the Problem
The question is asking which alkyl bromide isomer will undergo an Sn2 reaction most readily, indicating an evaluation of the reaction mechanism and the structure of the given compounds.
Answer
4-bromo-1-butene
The final answer is b) 4-bromo-1-butene.
Answer for screen readers
The final answer is b) 4-bromo-1-butene.
More Information
4-bromo-1-butene undergoes SN2 reactions most readily due to having a primary carbon with minimal steric hindrance, allowing the nucleophile easy access to the reaction center.
Tips
Avoid choosing tertiary or hindered secondary carbons for SN2 reactions as they increase steric hindrance.
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