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1. TsCl.pyridine CH,OH 2. CH,CH,CH,S-

1. TsCl.pyridine CH,OH 2. CH,CH,CH,S-

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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. Thank you for your help!
Consider the reaction between an alcohol and to expected main organic product. 1. TSCL.pyridine CH,OH 2. CH,CH,CH,S- SPECIAL AEQ λμπ (s) (1) (aq) (g)
Transcribed Image Text:Consider the reaction between an alcohol and to expected main organic product. 1. TSCL.pyridine CH,OH 2. CH,CH,CH,S- SPECIAL AEQ λμπ (s) (1) (aq) (g)
Attempt 11 y a nucleop < 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 CH, CH, rather than C, H,. contact us helo
Transcribed Image Text:Attempt 11 y a nucleop < 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 CH, CH, rather than C, H,. contact us helo
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