Deck 16: Carbohydrates
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Deck 16: Carbohydrates
1
Which of the following can be classified as a ketohexose?
_
A) 1
B) 2
C) 3
D) 4
E) 1, 3, and 4
_A) 1
B) 2
C) 3
D) 4
E) 1, 3, and 4
2
2
Which of the following can be classified as an aldopentose? 
A) 1
B) 2
C) 3
D) 4
E) 3 and 4

A) 1
B) 2
C) 3
D) 4
E) 3 and 4
1
3
Which of the following can be considered a polysaccharide?
A) sucrose
B) cellobiose
C) lactose
D) maltose
E) cellulose
A) sucrose
B) cellobiose
C) lactose
D) maltose
E) cellulose
cellulose
4
Glucose can be classified as a:
A) monosaccharide
B) disaccharide
C) trisaccharide
D) polysaccharide
E) table sugar
A) monosaccharide
B) disaccharide
C) trisaccharide
D) polysaccharide
E) table sugar
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5
The linkage between the sugar units in starch are:
A) ( )
B) ( )
C) ( )
D)( )
E) none of these
A) ( )
B) ( )
C) ( )
D)( )
E) none of these
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6
The acyclic structure of D-glucose is:
The formula for ethyl -D-glucopyranoside is:
A)
B)
C)
D)
E)
The formula for ethyl -D-glucopyranoside is:A)

B)

C)

D)

E)

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7
Reduction of an optically active aldopentose with NaBH4 gives an optically inactive alditol.The aldopentose could be:
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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8
Another name for the disaccharide, 4-O-( -D-galactopyranosyl)- -glucopyranose, is:
A) sucrose
B) cellobiose
C) lactose
D) maltose
E) amylose
A) sucrose
B) cellobiose
C) lactose
D) maltose
E) amylose
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9
A 1,4- -linkage between two glucose units produces a disaccharide called:
A) dextrose
B) cellobiose
C) ribose
D) maltose
E) amylose
A) dextrose
B) cellobiose
C) ribose
D) maltose
E) amylose
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10
A 1,4- -linkage between two glucose units produces a disaccharide called:
A) dextrose
B) cellobiose
C) ribose
D) maltose
E) amylose
A) dextrose
B) cellobiose
C) ribose
D) maltose
E) amylose
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11
Which of the following structures represent glycosides? 
A) only 1
B) only 2
C) only 3
D) 1 and 2
E) 1, 2, and 3

A) only 1
B) only 2
C) only 3
D) 1 and 2
E) 1, 2, and 3
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12
Hydrolysis of the disaccharide maltose produces: 
A) sucrose
B) glucose
C) mannose
D) glucose and fructose
E) glucose and galactose

A) sucrose
B) glucose
C) mannose
D) glucose and fructose
E) glucose and galactose
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13
The difference between the pyranose and furanose forms of a given aldohexose is:
A) the ring size
B) the number of the anomeric C
C) the type of functional groups
D) the number of functional groups
E) there is no difference
A) the ring size
B) the number of the anomeric C
C) the type of functional groups
D) the number of functional groups
E) there is no difference
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14
The formula for maltose is:
The acetal carbon(s) is(are):
A) C1
B) C1 and C1'
C) C1 and C4
D) C1'
E) C1' and C4'
The acetal carbon(s) is(are):A) C1
B) C1 and C1'
C) C1 and C4
D) C1'
E) C1' and C4'
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15
How many hydroxyl groups are present in the pyranose form of glucose?
A) 1
B) 2
C) 3
D) 4
E) 5
A) 1
B) 2
C) 3
D) 4
E) 5
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16
Which of the following can be classified as epimers? 
A) 1 and 2
B) 1 and 3
C) 1 and 4
D) 3 and 4
E) none are epimers

A) 1 and 2
B) 1 and 3
C) 1 and 4
D) 3 and 4
E) none are epimers
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17
The anomeric carbon of
is:
A) C1
B) C2
C) C3
D) C5
E) C6
is:A) C1
B) C2
C) C3
D) C5
E) C6
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18
The Haworth projection formula for the pyranose form of -D-galactose is: 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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19
D-Glucose can exist in how many isomeric cyclic hemiacetal forms?
A) 1
B) 2
C) 3
D) 4
E) 5
A) 1
B) 2
C) 3
D) 4
E) 5
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20
Which of the following can be considered reducing sugars? 
A) 1
B) 2
C) 3
D) 4
E) 1, 2, 3, and 4

A) 1
B) 2
C) 3
D) 4
E) 1, 2, 3, and 4
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21
The product of the reaction below is: 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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22
How many stereogenic centers are in the -cyclic form of glucose?
A) 1
B) 2
C) 3
D) 4
E) 5
A) 1
B) 2
C) 3
D) 4
E) 5
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23
Acid-catalyzed hydrolysis of
gives:
A)
B)
C)
D)
E)
gives:A)

B)

C)

D)

E)

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24
The anomeric carbon in the structure below is numbered: 
A) 1
B) 2
C) 3
D) 4
E) 5

A) 1
B) 2
C) 3
D) 4
E) 5
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25
The term that best describes the relationship between
is
A) conformers.
B) epimers.
C) enantiomers.
D) meso forms.
E) constitutional isomers.
isA) conformers.
B) epimers.
C) enantiomers.
D) meso forms.
E) constitutional isomers.
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26
The product of
is:
A)
B)
C)
D)
E)
is:A)

B)

C)

D)

E)

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27
Reduction of which of the following aldoses provides an optically active alditol? 
A) 1
B) 2
C) 3
D) 1 and 2
E) 3 and 4

A) 1
B) 2
C) 3
D) 1 and 2
E) 3 and 4
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28
The following monosaccharide has ________ equatorial hydroxyl groups.
_
A) 1
B) 2
C) 3
D) 4
E) 5
_A) 1
B) 2
C) 3
D) 4
E) 5
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29
D-Glucose reacts with acetic anhydride to produce:
A) ethers
B) esters
C) carboxylic acids
D) alcohols
E) aldehydes
A) ethers
B) esters
C) carboxylic acids
D) alcohols
E) aldehydes
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30
Starch is a polysaccharide that is found in many food sources.When starch is completely hydrolyzed, the monosaccharide that is produced is:
A) glucose
B) mannose
C) maltose
D) galactose
E) amylose
A) glucose
B) mannose
C) maltose
D) galactose
E) amylose
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31
The equilibrium rotation of an aqueous solution of - and -D-glucose is +50°, and the rotations of the pure and forms are +102° and +24°, respectively. Assuming no other forms are present, the percent form at equilibrium is:
A) 66.7%
B) 50.0%
C) 22.5%
D) 33.3%
E) 24.0%
A) 66.7%
B) 50.0%
C) 22.5%
D) 33.3%
E) 24.0%
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32
Treatment of D-(+)-mannose with Fehling's reagent (Cu+2) gives: 
A) an aldose
B) a ketose
C) an alditol
D) an aldonic acid
E) an aldaric acid

A) an aldose
B) a ketose
C) an alditol
D) an aldonic acid
E) an aldaric acid
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33
Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below).What is the structure of D-erythrose? 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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34
The configurations at C2, C3, and C4 of
are:
A) 2R, 3R, 4R
B) 2R, 3S, 4R
C) 2S, 3R, 4S
D) 2S, 3R, 4R
E) 2R, 3S, 4S
are:A) 2R, 3R, 4R
B) 2R, 3S, 4R
C) 2S, 3R, 4S
D) 2S, 3R, 4R
E) 2R, 3S, 4S
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35
The pyranose form of glucose is a(n):
A) linear aldehyde
B) cyclic hemiacetal
C) cyclic acetal
D) acyclic acetal
E) acyclic hemiacetal
A) linear aldehyde
B) cyclic hemiacetal
C) cyclic acetal
D) acyclic acetal
E) acyclic hemiacetal
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36
Hydrolysis of lactose gives:
A) glucose and galactose
B) glucose and fructose
C) mannose and fructose
D) galactose and fructose
E) allose and mannose
A) glucose and galactose
B) glucose and fructose
C) mannose and fructose
D) galactose and fructose
E) allose and mannose
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37
A glycoside is formed upon reaction of glucopyranose with:
A) KMnO4
B) HNO3
C) Cu+2/OH-
D) CH3OH/H+
E) NaBH4
A) KMnO4
B) HNO3
C) Cu+2/OH-
D) CH3OH/H+
E) NaBH4
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38
Which of the following reagents will convert the hydroxyl groups of a monosaccharide to methyl ethers?
A) H2/Ni
B) Ag2O/CH3I
C) HNO3
D) NaBH4/H2O
E) Br2/H2O
A) H2/Ni
B) Ag2O/CH3I
C) HNO3
D) NaBH4/H2O
E) Br2/H2O
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39
The difference between and -glucopyranose is:
A) the stereochemistry at the anomeric carbon
B) the number of carbons in the ring
C) the position of all the OH's on the ring
D) all of these reasons
E) none of these reasons
A) the stereochemistry at the anomeric carbon
B) the number of carbons in the ring
C) the position of all the OH's on the ring
D) all of these reasons
E) none of these reasons
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40
A Newman projection formula for
is:
A)
B)
C)
D)
E)
is:A)

B)

C)

D)

E)

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41
The product of the following reaction sequence is: 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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42
Which of the following compounds will give a positive Tollens' test (silver mirror)?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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43
Which of the following reagents will oxidize an aldose to an aldaric acid?
A) HNO3
B) Br2, H2O
C) NaBH4
D) PCC
E) Tollens' reagent
A) HNO3
B) Br2, H2O
C) NaBH4
D) PCC
E) Tollens' reagent
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44
The structure of an L-aldotetrose that would give an optically inactive alditol upon reduction with sodium borohydride (NaBH4) is:
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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45
Treatment of methyl -D-glucopyranose with silver oxide and iodomethane (Ag2O, CH3I) followed by hydrolysis (H3O+)
gives:
A)
B)
C)
D)
E)
gives:A)

B)

C)

D)

E)

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46
An intermediate in the following glycoside hydrolysis is: 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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