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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. Write the condensed formula of the expected main organic product.

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
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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.

The image shows a chemical reaction sequence involving ethanol (\(\text{CH}_3\text{CH}_2\text{OH}\)). **Reaction Steps:** 1. The first step involves the treatment of ethanol with tosyl chloride (TsCl) and pyridine. This step converts the alcohol group into a tosylate, making it a better leaving group. 2. In the second step, the tosylate is treated with iodide ion (\(\text{I}^-\)). This results in the substitution of the tosylate group with an iodide ion. This sequence illustrates a nucleophilic substitution reaction where an alcohol is converted to an alkyl iodide via a tosylate intermediate.
Transcribed Image Text:The image shows a chemical reaction sequence involving ethanol (\(\text{CH}_3\text{CH}_2\text{OH}\)). **Reaction Steps:** 1. The first step involves the treatment of ethanol with tosyl chloride (TsCl) and pyridine. This step converts the alcohol group into a tosylate, making it a better leaving group. 2. In the second step, the tosylate is treated with iodide ion (\(\text{I}^-\)). This results in the substitution of the tosylate group with an iodide ion. This sequence illustrates a nucleophilic substitution reaction where an alcohol is converted to an alkyl iodide via a tosylate intermediate.
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