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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Complete the reaction.

Transcribed Image Text:The image displays a chemical reaction involving an acetic acid derivative. The structure on the left is a carboxylic acid, specifically acetic acid, with the molecular formula CH₃COOH. The carbonyl carbon is bonded to a hydroxyl group (-OH).
The reaction proceeds in two steps:
1. The first step involves the use of sodium hydride (NaH). Sodium hydride is a strong base, which will deprotonate the hydroxyl group of the carboxylic acid, resulting in a carboxylate anion.
2. In the second step, the carboxylate anion reacts with bromoethane (CH₃CH₂Br). This step likely involves a nucleophilic substitution reaction, where the ethyl group from bromoethane replaces the bromine atom.
This sequence of reactions suggests the formation of an ester, specifically ethyl acetate, through nucleophilic acyl substitution.
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