Carbohydrates Flashcards
Which of the following monosaccharides is a ketose?
a. glucose
b. fructose
c. galactose
d. mannose
b
Which of the following monosaccharides is an aldose
a. glucose
b. galactose
c. mannose
d. ribose
e. all of them
e
Which of the following monosaccharides is a ketose?
a. arabinose
b. ribose
c. xylose
d. lyxose
e. none of them
e
Haworth projection formulas
a. are representations of the cyclic form of sugars
b. can show the distinction between the α and β anomers
c. both of the above
d. neither of the above
c
Which of the following is not a function of carbohydrates?
a. They are major energy sources.
b. They play key roles in processes that take place on the surface of cells.
c. They are used in structural roles.
d. They are catalytic components of enzymes.
d
How many carbon atoms are in the simplest carbohydrates?
a. 1
b. 2
c. 3
d. 4
e. 5
c
The simplest ketotriose is
a. glyceraldehyde.
b. dihydroxyacetone.
c. ribose.
d. glucose.
e. sucrose.
b
Mirror image stereoisomers are called
a. anomers.
b. diastereoisomers.
c. enantiomers.
d. epimers.
c
The simplest aldotriose is:
a. acetone
b. dihydroxyacetone
c. glyceraldehyde
d. threose
c
In a Fischer projection, which chiral carbon determines whether the sugar is the D- or the L-isomer?
a. highest numbered carbon atom
b. lowest numbered asymmetric carbon atom
c. lowest numbered carbon atom
d. highest numbered asymmetric carbon atom
d
….OH
|
H-C-H
|
C=O
|
H-C-OH
|
HO-C-H
|
H-C-OH
|
H-C-H
|
OH
The carbohydrate shown is
a. a monosaccharide
b. a ketose.
c. a hexose.
d. all of these
e. none of these
d
….OH
|
H-C-H
|
C=O
|
H-C-OH
|
HO-C-H
|
H-C-OH
|
H-C-H
|
OH
The carbohydrate shown is
a. the D isomer.
b. the L isomer.
c. both D and L.
d. neither D nor L.
e. It’s impossible to tell from a picture which isomer this is.
a
For the α anomer of a D-sugar, the anomeric hydroxyl in a Haworth projection
a. has an upward projection (on the same side as the terminal CH2OH group).
b. has a downward projection (on the opposite side from the terminal CH2OH group).
c. may be either up or down, it depends on the individual sugar.
d. is non-existent; anomers are a consideration only in Fischer projections.
b
Diastereomers are
a. mirror-image, nonsuperimposable stereoisomers.
b. non-mirror-image, nonsuperimposable stereoisomers.
c. stereoisomers with one or more double bonds.
d. none of the above.
b
Epimers are
a. stereoisomers that differ from each other in their configuration at two or more carbon atoms.
b. stereoisomers that differ from each other in their configuration at a single carbon atom.
c. the α and β forms of cyclic sugars.
d. two related compounds, pyran and furan
b
D-erythrose is to D-ribose
as D-ribose is to:
a. D-allose
b. D-altrose
c. D-glucose
d. D-galactose
a
How many enantiomeric pairs are possible for a aldohexose?
a. 2
b. 4
c. 8
d. 16
c
Sugars which differ in chirality only around one carbon are most specifically called
a. anomers.
b. diastereoisomers.
c. enantiomers.
d. epimers.
e. none of these
d
Aldoses can form which type of cyclic structure?
a. Hemiacetal
b. Hemiketal
c. Both hemiacetal and hemiketal
d. Neither hemiacetal and hemiketal
a
The cyclic form of sugars
a. has one more chiral center (the anomeric carbon) than the open-chain form.
b. loses a chiral center compared to the open-chain form.
c. is not usually found in nature.
d. has one more carbon atom than the open-chain form.
e. has one less carbon atom than the open-chain form.
a
The enantiomer of D-glucose is:
a. D-Fructose
b. D-Glucose
c. L-Glucose
d. L-Idose
e. D-Galactose
c
Epimers of D-Glucose include:
a. D-Fructose and L-Glucose
b. D-Glucose and L-Glucose
c. L-Glucose and L-Idose
d. L-Idose and D-Galactose
e. L-Glucose and D-Galactose
d
Diastereoisomers of D-Glucose include all of these, except:
a. D-Fructose
b. L-Glucose
c. L-Idose
d. D-Galactose
e. All of these are diastereoisomers of D-Glucose.
a
Isomers of sugars in which the position of ketone and aldehyde groups have been changed are called
a. anomers.
b. diastereoisomers.
c. enantiomers.
d. epimers.
e. none of these
e
Which carbon of the open-chain form of a sugar becomes the anomeric carbon in the cyclic form?
a. the carbonyl carbon
b. the highest numbered chiral center
c. the highest numbered carbon
d. It depends on the individual sugar.
a
The α and β forms of the same sugar are called
a. anomers.
b. diastereoisomers.
c. enantiomers.
d. epimers.
e. none of these
a
A pyranose is a sugar that
a. contains a five-membered ring as part of its cyclic structure.
b. contains a six-membered ring as part of its cyclic structure.
c. is a five-carbon open-chain sugar.
d. is a six-carbon open-chain sugar.
b
A furanose is a sugar that
a. contains a five-membered ring as part of its cyclic structure.
b. contains a six-membered ring as part of its cyclic structure.
c. is a five-carbon open-chain sugar.
d. is a six-carbon open-chain sugar.
a
For a D-sugar, any group that is written to the right of the carbon in a Fischer projection
a. has an upward projection in a Haworth projection.
b. has a downward projection in a Haworth projection.
c. may be either up or down in a Haworth projection, it depends on the individual sugar.
d. is missing from a Haworth projection.
b
Which of the following groups is produced when an aldehyde is oxidized?
a. ketone
b. carboxyl
c. alcohol
d. ether
b
A lactone is a cyclic
a. ether.
b. ester.
c. ketone.
d. alcohol.
b
Which of the following compounds is produced by oxidation of an aldose in the cyclic form?
a. a hemiacetal
b. a hemiketal
c. a lactone
d. an amino sugar
c
Two samples containing identical mixtures of sugars are analyzed, one using Tollen’s reagent, the other with glucose
oxidase. Which will give a stronger reaction?
a. Tollen’s reagent
b. glucose oxidase
c. They will have identical strengths.
d. It’s impossible to predict from the information provided.
a
The conversion of a sugar’s carbonyl to an alcohol is
a. a reduction reaction.
b. an oxidation reaction.
c. a glycosidic reaction.
d. impossible.
a
Deoxyribose is best described as a(n):
a. oxidized form of ribose
b. reduced pyranose
c. polyhydroxyl alcohol
d. glycoside
e. reduced form of a pentose
e
When monosaccharides are bonded together
a. one H2O molecule is lost for each new link formed.
b. oligosaccharides are formed by combining a few monosaccharides.
c. polysaccharides are formed by combining many monosaccharides.
d. all of these
d