Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 24.9C, Problem 24.20P
Interpretation Introduction
Interpretation: The third and fourth steps in the sequencing of oxytocin are to be determined.
Concept introduction: Oxytocin is defined as a hormone which is present in the brain and plays a role in childbirth due to the muscles contraction in the womb.
To determine: The third and fourth steps in the sequencing of oxytocin.
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a. Determine whether each of the Followery
Molecules
is in
the R- On the y-
Configuration
1-01"/
1-6-4
Br
4
I
el
Br
b. Draw The Fisher projection For all the
Meso compounds that can
exist FOR
The Following molenle
1- Refer to the monosaccharides below to answer each of the following question(s):
CH₂OH
CHO
CH₂OH
CH₂OH
0
H-
OH
0
0
HO-
H
H-
-OH
HO
H
HO H
H OH
HO- H
CH₂OH
H.
OH
HO
H
HO-
H
CH₂OH
CH₂OH
CH3
a. Sorbose
b. Rhamnose
c. Erythrulose
d. Xylulose
Classify each sugar by type; for example, glucose is an aldohexose.
a. Xylulose is ..
b. Erythrulose is .
c. Sorbose is ..
d. Rhamnose is ..
2- Consider the reaction below to answer the following question(s).
CHO
H
OH
CH₂OH
CH₂OH
HO-
H
HO
HO
+
H.
-OH
HO
OH
HO.
H
OH
OH
H
-OH
H
OH
CH₂OH
Q
Z
a.
Refer to Exhibit 25-11. Place a triangle around the anomeric carbon in compound Q.
Compound Z is:
b.
1. the D-anomer.
2. the a-anomer.
3. the ẞ-anomer.
4. the L-anomer.
c. Which anomer is the LEAST stable?
d. Q and Z are cyclic examples of:
a. acetals
b.
hemiacetals
c. alditols
d.
hemialditols
Chapter 24 Solutions
Organic Chemistry (9th Edition)
Ch. 24.2A - Draw three-dimensional representations of the...Ch. 24.2A - Prob. 24.2PCh. 24.2B - The herbicide glyphosate (Roundup) kills plants by...Ch. 24.4 - Draw the structure of the predominant form of a....Ch. 24.4 - Draw the resonance forms of a protonated guanidino...Ch. 24.4 - Although tryptophan contains a heterocyclic amine,...Ch. 24.4 - Prob. 24.7PCh. 24.4 - Prob. 24.8PCh. 24.5A - Show how the following amino acids might be formed...Ch. 24.5B - Prob. 24.10P
Ch. 24.5C - Prob. 24.11PCh. 24.5C - Show how you would use a Strecker synthesis to...Ch. 24.6 - Suggest how you would separate the free i-ammo...Ch. 24.7A - Propose a mechanism for the acid-catalyzed...Ch. 24.7A - Give equations for the formation and...Ch. 24.7B - Prob. 24.16PCh. 24.7C - Prob. 24.17PCh. 24.8B - Draw the complete structures of the following...Ch. 24.9C - Prob. 24.19PCh. 24.9C - Prob. 24.20PCh. 24.9C - Prob. 24.21PCh. 24.9E - Prob. 24.22PCh. 24.9E - Prob. 24.23PCh. 24.10A - Propose a mechanism for the coupling of acetic...Ch. 24.10B - Show how you would synthesize Leu-Gly-Ala-Val-Phe...Ch. 24.10B - Show how solid-phase peptide synthesis would be...Ch. 24 - a. The isoelectric point (pl) of phenylalanine is...Ch. 24 - Prob. 24.28SPCh. 24 - Prob. 24.29SPCh. 24 - Prob. 24.30SPCh. 24 - Prob. 24.31SPCh. 24 - Suggest a method for the synthesis of the...Ch. 24 - Prob. 24.33SPCh. 24 - Write the complete structures for the following...Ch. 24 - The following structure is drawn in an...Ch. 24 - Prob. 24.36SPCh. 24 - Prob. 24.37SPCh. 24 - Show the steps and intermediates in the synthesis...Ch. 24 - Prob. 24.39SPCh. 24 - Lipoic acid is often found near the active sites...Ch. 24 - Prob. 24.41SPCh. 24 - Prob. 24.42SPCh. 24 - Prob. 24.43SPCh. 24 - Complete hydrolysis of an unknown basic...Ch. 24 - Prob. 24.45SPCh. 24 - Prob. 24.46SPCh. 24 - Prob. 24.47SP
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