Cuyamaca College Chemistry Multiple Choice Questions Hello, this assignment is short, 11multiple choice and open questionsplease answer all questions with explanation as to why that is the answer.for the writing portion of the assignment please give great detail and no plagiarism.and of course A+ material. QUESTION 1
Which structure represents a deoxyfuranose sugar?
О.
ОН
ОН
о
ОН
ОН
D:
А:
В:
C:
НО
“ОН
HO
HONY
“ОН
НО
НО
ОН
ОН
НО
A
В
С
D
4 points
QUESTION 2
Which the following structures is a reducing sugar?
ОН
НО
НО,
ОН
ОН
А:
НО
С:
D:
ОН
о
О
НО”
О
ОН
ОН
НО
НО
HO…
НО.
оно
ОН
НО
НО
НО
ОН
ОН
НО
”
“ОН
ОН
СА
В
C
D
QUESTION 3
4
Reducing carbohydrates can react with amines under physiological conditions by a glycation reaction. What functional group forms when an aldose
reacts?
amine
amide
imine
enamine
QUESTION 6
Which structure represents the correct protonation state at physiological pH?
A:
НО
Он в: o
D:
HO
0
NH2
NH3+
NH3+
A А.
B
C
D
QUESTION 7
What product results when this carbohydrate derivative is treated with catalytic acid in acetone?
OCH3
OCH3 A:
..OCH3
B:
C:
“OCH3
HO
OH
carbohydrate deriative
starting material
A
B
С
None of the above
QUESTION 8
Which amino acid will be anionic a physiological pH?
A
:
N
pon Birnom lon ci rien Divoli
HN
NH2
ОА
B
с
D
QUESTION 9
Why are protecting groups necessary when generating polypeptides?
Amines and carboxylic acids are unreactive without the use of protecting groups.
Amino acids are multifuctional molecules and the reactivity needs to be limited to the amine and carboxylic acid that are to form the desired
amide bond.
Amino acids are too reactive and need to be modulated in the reactivity.
Protecting groups are unnecessary in polypeptide synthesis.
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