Compare the stability of the two salt bridges shown circled in blue at pH 8.4. The carboxylate ions are completely de- protonated at pH 8.4 The pka of the amino group (upper left) is 8.1 and the pka of the amino group (bottom right) is 8.7. 9 5-6- CH₂COOH (0 H--O=C (b) KHANH, The bottom right salt bridge is stronger due to the partial positive charge of +2/3. The bottom right salt bridge is stronger due to the partial positive charge of +1/3. The upper left salt bridge is stronger due to the partial positive charge of +1/3. The upper left salt bridge is stronger due to the partial positive charge of +2/3.
Compare the stability of the two salt bridges shown circled in blue at pH 8.4. The carboxylate ions are completely de- protonated at pH 8.4 The pka of the amino group (upper left) is 8.1 and the pka of the amino group (bottom right) is 8.7. 9 5-6- CH₂COOH (0 H--O=C (b) KHANH, The bottom right salt bridge is stronger due to the partial positive charge of +2/3. The bottom right salt bridge is stronger due to the partial positive charge of +1/3. The upper left salt bridge is stronger due to the partial positive charge of +1/3. The upper left salt bridge is stronger due to the partial positive charge of +2/3.
Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
Related questions
Question
![Compare the stability of the two salt bridges
shown circled in blue at pH 8.4. The
carboxylate ions are completely de-
protonated at pH 8.4 The pka of the amino
group (upper left) is 8.1 and the pka of the
amino group (bottom right) is 8.7.
(d)
NH,
F-8-
Ed
(b)
O-H-
M5
CH₂COOH
(c) 5
(b)
CH,
CH.
H--O=C
(d)
-H
H
CH,OH
(b)
KCHJ NH,
(a)
The bottom right salt bridge is stronger
due to the partial positive charge of +2/3.
The bottom right salt bridge is stronger
due to the partial positive charge of +1/3.
The upper left salt bridge is stronger due
to the partial positive charge of +1/3.
The upper left salt bridge is stronger due
to the partial positive charge of +2/3.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F940a64b6-a53e-4bc6-85b0-cc0b37fb57fe%2Fb7d82124-4d97-42d9-9574-6ae4a2b6b285%2Fsruqw65_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Compare the stability of the two salt bridges
shown circled in blue at pH 8.4. The
carboxylate ions are completely de-
protonated at pH 8.4 The pka of the amino
group (upper left) is 8.1 and the pka of the
amino group (bottom right) is 8.7.
(d)
NH,
F-8-
Ed
(b)
O-H-
M5
CH₂COOH
(c) 5
(b)
CH,
CH.
H--O=C
(d)
-H
H
CH,OH
(b)
KCHJ NH,
(a)
The bottom right salt bridge is stronger
due to the partial positive charge of +2/3.
The bottom right salt bridge is stronger
due to the partial positive charge of +1/3.
The upper left salt bridge is stronger due
to the partial positive charge of +1/3.
The upper left salt bridge is stronger due
to the partial positive charge of +2/3.
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