The following questiowatch the provided video, A Mechanism for Preparation of Sulfides from Thiols by David Klein, andanswer the questions below.Question 1The preparation of a sulfide from a thiol is analogous to the Williamson ether synthesis. Which ofthe following describes the mechanism of this transformation?O Three steps: 1) protonation; loss of leaving group; 3) nucleophilic attack.O Deprotonation, followed by SN2.O Three steps: 1) deprotonation; 2) loss of leaving group: 3) nucleophilic attack.O SN2, followed by deprotonation.O Three steps: 1) loss of leaving group; 2) nucleophilic attack; 3) deprotonation.Save for LaterAttempts: 0 of 2 used Submit Answer

The sulfide can take place by the reaction of the thiol and alkyl halide. The deprotonated thiol…

The preparation of a sulfide from a thiol is analogous to the Williamson ether synthesis. Which of the following describes the mechanism of this transformation? O Three steps: 1) protonation; 2) loss of leaving group; 3) nucleophilic attack. O Deprotonation, followed by SN2. O Three steps: 1) deprotonation; 2) loss of leaving group: 3) nucleophilic attack. O SN2, followed by deprotonation. O Three steps: 1) loss of leaving group; 2) nucleophilic attack; 3) deprotonation.

The preparation of a sulfide from a thiol is analogous to the Williamson ether synthesis. Which of the following describes the mechanism of this transformation? O Three steps: 1) protonation; 2) loss of leaving group; 3) nucleophilic attack. O Deprotonation, followed by SN2. O Three steps: 1) deprotonation; 2) loss of leaving group: 3) nucleophilic attack. O SN2, followed by deprotonation. O Three steps: 1) loss of leaving group; 2) nucleophilic attack; 3) deprotonation.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 47AP

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