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 toexpected main organic product.1. TSCL.pyridineCH,OH2. CH,CH,CH,S-SPECIALAEQλμπ(s)(1)(aq)(g) Attempt 11y a nucleop <FeedbackThe first step of the reactionproduces a tosylate ester, TSOR. Thetosylate group is a better leavinggroup than the hydroxyl group in theinitial alcohol.Be sure that the formula is notcondensed. For example, writeCH, CH, rather than C, H,.contact ushelo

Step 1 : In the first step of reaction alcohol is activated by being converted into sulphonate…

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

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

Introductory Chemistry: A Foundation

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ISBN:9781337399425

Author:Steven S. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Donald J. DeCoste

Chapter19: Radioactivity And Nuclear Energy

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Question

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)

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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