What is the most acidie proton in methanol, CH;OH (H, or H,)? Explain briefly (CB = Conjugate Base). н, о-с-н H. A) H, is more acidic. Because carbon is less electronegative, CB-b is more stable than CB-a. B) H, is more acidic. Because carbon is less clectronegative, H, is more stable than Hp. C) H, is more acidic. Because oxygen is more electronegative, CB-a is more stable than CB-b. D) H, is more acidic. Because oxygen is more electronegative, H, is more stable than H. E) H, is more acidic. Because oxygen is more electronegative, H, is more stable than Hp.

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Chapter14: Acid-base Equilibria
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b My Questions | bartleby
O Dashboard
O Course: Chem 120 - Organic Che X
O LOCAL clicker
+
->
A cpp.edu/~Isstarkey/local/clicker/bonding/acid-base.html
What is the most acidic proton in methanol, CHOH
Which is the stronger base? Explain briefly.
(H, or H,)? Explain briefly (CB = Conjugate Base).
NH3
NH2
H-0-C-H
H.
ammonia
aniline
A) H, is more acidic. Because carbon is less
clectronegative, CB-b is more stable than CB-a.
A) Because this is more stable:
aniline is the stronger base.
-NH2
B) H, is more acidic. Because carbon is less
electronegative, H, is more stable than Hp-
B) Because this is more stable:
ammonia is the stronger base.
-NH2
C) H, is more acidie. Because oxygen is more
electronegative, CB-a is more stable than CB-b.
C) Because this is more stable: NH3
aniline is the stronger base.
D) H, is more acidic. Because oxygen is more
electronegative, H, is more stable than Hp.
D) Because this is more stable: NH2
ammonia is the stronger base.
E) H, is more acidic. Because oxygen is more
electronegative, H, is more stable than Hp.
E) Because this is more stable:
aniline is the stronger base. NH
Inductive withdrawal of electron density (as shown
below) has what effect on the negative charge?
Which of the following is classified as a
conjugate acid-base pair?
A) HCI / NaOH
B) H3O¨/ H20
C) 02/ H20
D) H*/ CI*
A) It's a good thing (stabilizing) for the negative charge.
E) NaCl / NaOH
B) It's a bad thing (destabilizing) for the negative charge.
*2GRE
C) It has no effect on the negative charge.
8:11 PM
(ll ENG
2/23/2021
Transcribed Image Text:b My Questions | bartleby O Dashboard O Course: Chem 120 - Organic Che X O LOCAL clicker + -> A cpp.edu/~Isstarkey/local/clicker/bonding/acid-base.html What is the most acidic proton in methanol, CHOH Which is the stronger base? Explain briefly. (H, or H,)? Explain briefly (CB = Conjugate Base). NH3 NH2 H-0-C-H H. ammonia aniline A) H, is more acidic. Because carbon is less clectronegative, CB-b is more stable than CB-a. A) Because this is more stable: aniline is the stronger base. -NH2 B) H, is more acidic. Because carbon is less electronegative, H, is more stable than Hp- B) Because this is more stable: ammonia is the stronger base. -NH2 C) H, is more acidie. Because oxygen is more electronegative, CB-a is more stable than CB-b. C) Because this is more stable: NH3 aniline is the stronger base. D) H, is more acidic. Because oxygen is more electronegative, H, is more stable than Hp. D) Because this is more stable: NH2 ammonia is the stronger base. E) H, is more acidic. Because oxygen is more electronegative, H, is more stable than Hp. E) Because this is more stable: aniline is the stronger base. NH Inductive withdrawal of electron density (as shown below) has what effect on the negative charge? Which of the following is classified as a conjugate acid-base pair? A) HCI / NaOH B) H3O¨/ H20 C) 02/ H20 D) H*/ CI* A) It's a good thing (stabilizing) for the negative charge. E) NaCl / NaOH B) It's a bad thing (destabilizing) for the negative charge. *2GRE C) It has no effect on the negative charge. 8:11 PM (ll ENG 2/23/2021
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