1. Answer parts a) through e) for each sugar A through E below. 每 A= A= COOH CHO H- -OH € € OH -OH H H- -OH -OH CH₂OH CH₂OPO, C B D a) Classify each sugar A through E by the number of carbons (e.g. triose, tetrose, etc.). A= 8 = A= B = C= B = HO b) Classify each sugar by type of carbonyl group (i.e. aldose, ketose, aldonic acid, or uronic acid). Some carbonyl groups may be shown in a masked form, e.g. hemiacetal or hemiketal; in such cases, write hemiacetal or hemiketal. If no carbonyl, hemiacetal, or hemiketal is present, write "N/A". C = B = OH C= D= C= c) Classify each sugar by the class of derivative (i.e. aldonic acid, uronic acid, amino sugar, deoxy sugar, alditol, sugar phosphate). If no derivative is given, then write "N/A". M₂N D= OH CH₂OH HO- HO -H 睡 H- -OH H- -OH CH₂OH E D= E= d) Classify each sugar by its ring form, e.g. pyranose or furanose. If no ring form is given, write "N/A". E= E= E=
1. Answer parts a) through e) for each sugar A through E below. 每 A= A= COOH CHO H- -OH € € OH -OH H H- -OH -OH CH₂OH CH₂OPO, C B D a) Classify each sugar A through E by the number of carbons (e.g. triose, tetrose, etc.). A= 8 = A= B = C= B = HO b) Classify each sugar by type of carbonyl group (i.e. aldose, ketose, aldonic acid, or uronic acid). Some carbonyl groups may be shown in a masked form, e.g. hemiacetal or hemiketal; in such cases, write hemiacetal or hemiketal. If no carbonyl, hemiacetal, or hemiketal is present, write "N/A". C = B = OH C= D= C= c) Classify each sugar by the class of derivative (i.e. aldonic acid, uronic acid, amino sugar, deoxy sugar, alditol, sugar phosphate). If no derivative is given, then write "N/A". M₂N D= OH CH₂OH HO- HO -H 睡 H- -OH H- -OH CH₂OH E D= E= d) Classify each sugar by its ring form, e.g. pyranose or furanose. If no ring form is given, write "N/A". E= E= E=
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
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Question
please help question 1, a-d
Correctly please.
![1. Answer parts a) through e) for each sugar A through E below.
$
A=
A=
COOH
OH
H-
-OH
€ €€
-OH
H-
-OH
CH₂OH
OH
B
a) Classify each sugar A through E by the number of carbons (e.g. triose, tetrose, etc.).
A=
8 =
A=
B =
H- -OH
B=
-OH
C=
B =
CHIOPO,
C
C=
D=
D
D=
-OH
b) Classify each sugar by type of carbonyl group (i.e. aldose, ketose, aldonic acid, or uronic acid). Some
carbonyl groups may be shown in a masked form, e.g. hemiacetal or hemiketal; in such cases, write hemiacetal
or hemiketal. If no carbonyl, hemiacetal, or hemiketal is present, write "N/A".
C=
HO
D=
HO
H-
E=
c) Classify each sugar by the class of derivative (i.e. aldonic acid, uronic acid, amino sugar, deoxy sugar, alditol,
sugar phosphate). If no derivative is given, then write "N/A".
E=
d) Classify each sugar by its ring form, e.g. pyranose or furanose. If no ring form is given, write "N/A".
CH₂OH
E=
-OH
-OH
E=
CH₂OH
E](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe3b22d41-205f-416f-a437-2c9a4d75fa28%2Fd15a1d54-5475-4d77-b35d-61b01520e561%2Fd4ippe_processed.jpeg&w=3840&q=75)
Transcribed Image Text:1. Answer parts a) through e) for each sugar A through E below.
$
A=
A=
COOH
OH
H-
-OH
€ €€
-OH
H-
-OH
CH₂OH
OH
B
a) Classify each sugar A through E by the number of carbons (e.g. triose, tetrose, etc.).
A=
8 =
A=
B =
H- -OH
B=
-OH
C=
B =
CHIOPO,
C
C=
D=
D
D=
-OH
b) Classify each sugar by type of carbonyl group (i.e. aldose, ketose, aldonic acid, or uronic acid). Some
carbonyl groups may be shown in a masked form, e.g. hemiacetal or hemiketal; in such cases, write hemiacetal
or hemiketal. If no carbonyl, hemiacetal, or hemiketal is present, write "N/A".
C=
HO
D=
HO
H-
E=
c) Classify each sugar by the class of derivative (i.e. aldonic acid, uronic acid, amino sugar, deoxy sugar, alditol,
sugar phosphate). If no derivative is given, then write "N/A".
E=
d) Classify each sugar by its ring form, e.g. pyranose or furanose. If no ring form is given, write "N/A".
CH₂OH
E=
-OH
-OH
E=
CH₂OH
E
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