Why do water-insoluble carboxylic acids dissolve in aqueous sodium hydroxide?

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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38. Why do water-insoluble carboxylic acids dissolve in
aqueous sodium hydroxide?
39. Briefly, but clearly, explain why the -OH hydrogen in
acetic acid (CH,CO,H) is more acidic than in ethanol
(СН,ОН).
40. Define a protic solvent.
arrow pushing mechanism to illustrate the
formation of t-butyl bromide from t-butanol and draw in
the necessary intermediates and products formed.
41. Draw an
CH2
CH3
Conjugate Acid
Conjugate Base
1
Dashboard
Calendar
Тo Do
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Transcribed Image Text:Search .l 4:35 PM < Вack Assignment #1.docx 38. Why do water-insoluble carboxylic acids dissolve in aqueous sodium hydroxide? 39. Briefly, but clearly, explain why the -OH hydrogen in acetic acid (CH,CO,H) is more acidic than in ethanol (СН,ОН). 40. Define a protic solvent. arrow pushing mechanism to illustrate the formation of t-butyl bromide from t-butanol and draw in the necessary intermediates and products formed. 41. Draw an CH2 CH3 Conjugate Acid Conjugate Base 1 Dashboard Calendar Тo Do Notifications Inbox
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