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
Chapter31: Introduction To Analytical Separations
Section: Chapter Questions
Problem 31.26QAP
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