1. This experiment is a multistep synthesis. In the first step as described in the textbook, acetanilide (1) reacts with chlorosulfonic acid to give p-acetamidobenzenesulfonyl chloride (2). HN HO-S-CI HN O=$=O ČI 1. To obtain pure (2), it is necessary to destroy the excess chlorosulfonic acid with water. Write the equation showing how chlorosulfonic acid reacts with water, Hint: water acts as a nucleonhile

1. This experiment is a multistep synthesis. In the first step as described in the textbook, acetanilide (1) reacts with chlorosulfonic acid to give p-acetamidobenzenesulfonyl chloride (2). HN HO-S-CI HN O=$=O ČI 1. To obtain pure (2), it is necessary to destroy the excess chlorosulfonic acid with water. Write the equation showing how chlorosulfonic acid reacts with water, Hint: water acts as a nucleonhile

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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