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SN2 Substitution at Secondary Halides and Sulfonates Is Often Complicated

question 5

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SN2 substitution at secondary halides and sulfonates is often complicated by competing E2 elimination.Which of the nucleophiles below would you choose to obtain the highest yield in an SN2 reaction with menthyl bromide? S<sub>N</sub>2 substitution at secondary halides and sulfonates is often complicated by competing E2 elimination.Which of the nucleophiles below would you choose to obtain the highest yield in an S<sub>N</sub>2 reaction with menthyl bromide?   A)  CH<sub>3</sub>ONa B)  CH<sub>3</sub>CO<sub>2</sub>Na C)  (CH<sub>3</sub>) <sub>3</sub>N D)  (CH<sub>3</sub>) <sub>3</sub>COK E)  C<sub>6</sub>H<sub>5</sub>SNa


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A profitability metric that accounts for all of a company's expenses except for interest and income taxes, reflecting the firm's profit.

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