Number 38 please l T-Mobile Wi-Fi4:41 PM< ВackAssignment #1.docx38. Why do water-insoluble carboxylic acids dissolve inaqueous sodium hydroxide?39. Briefly, but clearly, explain why the -OH hydrogen inacetic acid (CH;CO,H) is more acidic than in ethanol(С,Н,ОН).40. Define a protic solvent.arrow pushing mechanism to illustrate theformation of t-butyl bromide from t-butanol and draw inthe necessary intermediates and products formed.41. Draw anCH3H3COHHCH3Conjugate AcidConjugate Base1DashboardCalendarТo DoNotificationsInbox

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Why do water-insoluble carboxylic acids dissolve in aqueous sodium hydroxide? 38.

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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Question

Number 38 please

l T-Mobile Wi-Fi
4:41 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
(С,Н,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
CH3
H3C
OH
H
CH3
Conjugate Acid
Conjugate Base
1
Dashboard
Calendar
Тo Do
Notifications
Inbox

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