Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile Feedback expected main organic product. CH₂ CH₂OH 1. TsCl,pyridine 2. CH₂CH₂CH₂S™ CH₂CH₂CH₂ SHCH₂ CH3 Incorrect Macmillan Learning The first step of the reaction produces a tosylate ester, TSOR. The tosylate group is a better leaving group than the hydroxyl group in the initial alcohol. Be sure that the formula is not condensed. For example, write CH3CH₂ rather than C₂H₂.

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Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product.

 
Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile <
expected main organic product.
CH₂CH₂OH
1. TsCl,pyridine
2. CH₂CH₂CH₂S¯
CH₂CH₂CH₂SHCH₂CH²
Incorrect
Macmillan Learning
Feedback
×
The first step of the reaction produces a
tosylate ester, TSOR. The tosylate
group is a better leaving group than the
hydroxyl group in the initial alcohol.
Be sure that the formula is not
condensed. For example, write
CH₂ CH₂ rather than C₂H².
Transcribed Image Text:Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile < expected main organic product. CH₂CH₂OH 1. TsCl,pyridine 2. CH₂CH₂CH₂S¯ CH₂CH₂CH₂SHCH₂CH² Incorrect Macmillan Learning Feedback × The first step of the reaction produces a tosylate ester, TSOR. The tosylate group is a better leaving group than the hydroxyl group in the initial alcohol. Be sure that the formula is not condensed. For example, write CH₂ CH₂ rather than C₂H².
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