The following reaction is correct as shown. True False OH (xs) H

Chemistry
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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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**Question:**

The following reaction is correct as shown.

[Image of a chemical reaction]

**Reaction Description:**
- Reactants: 
  - Butanoic acid (\( \text{C}_4\text{H}_8\text{O}_2 \)) 
  - Dimethylamine (\( \text{(CH}_3)_2\text{NH} \)), in excess (denoted by "xs")

- Products:
  - Butanoate ion (\( \text{C}_4\text{H}_7\text{O}_2^-\))
  - Dimethylammonium ion (\( \text{(CH}_3)_2\text{NH}_2^+\))

**Options:**
- ☐ True
- ☐ False

**Explanation:**
This image shows a typical acid-base reaction mechanism. The carboxylic acid (\( \text{COOH} \)) donates a proton (H⁺) to the amine, forming the carboxylate ion and the ammonium ion. The reaction illustrates the transfer of a proton from butanoic acid to the nitrogen atom of dimethylamine, resulting in the formation of the respective conjugate base and acid.
Transcribed Image Text:**Question:** The following reaction is correct as shown. [Image of a chemical reaction] **Reaction Description:** - Reactants: - Butanoic acid (\( \text{C}_4\text{H}_8\text{O}_2 \)) - Dimethylamine (\( \text{(CH}_3)_2\text{NH} \)), in excess (denoted by "xs") - Products: - Butanoate ion (\( \text{C}_4\text{H}_7\text{O}_2^-\)) - Dimethylammonium ion (\( \text{(CH}_3)_2\text{NH}_2^+\)) **Options:** - ☐ True - ☐ False **Explanation:** This image shows a typical acid-base reaction mechanism. The carboxylic acid (\( \text{COOH} \)) donates a proton (H⁺) to the amine, forming the carboxylate ion and the ammonium ion. The reaction illustrates the transfer of a proton from butanoic acid to the nitrogen atom of dimethylamine, resulting in the formation of the respective conjugate base and acid.
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