Carbohydrates Flashcards
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) both of the above
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) They are catalytic components of enzymes.
The simplest ketotriose is:
a) glyceraldehyde.
b) dihydroxyacetone.
c) ribose.
d) glucose.
e) sucrose.
b) dihydroxyacetone.
For a D-sugar, the α anomer 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) has a downward projection (on the opposite side from the terminal CH2OH group).
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) non-mirror-image, nonsuperimposable stereoisomers.
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 a and b forms of cyclic sugars.
d) two related compounds, pyran and furan.
b) stereoisomers that differ from each other in their configuration at a single carbon atom.
How many stereoisomers are possible for an aldopentose?
a) 4
b) 8
c) 12
d) 16
b) 8
How many enantiomeric pairs are possible for an aldohexose?
a) 2
b) 4
c) 8
d) 16
c) 8
Aldose can form which type of cyclic structure?
a) Hemiacetal
b) Hemiketal
c) Both hemiacetal and hemiketal
d) Neither hemiacetal and hemiketal
a) Hemiacetal
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) has one more chiral center (the anomeric carbon) than the open-chain form.
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 the above.
e) none of the above.
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 carbonyl carbon
The α and β forms of the same sugar are called
a) anomers.
b) diastereoisomers.
c) enantiomers.
d) epimers.
e) none of the above.
a) anomers.
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) contains a six-membered ring as part of its cyclic structure.
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) contains a five-membered ring as part of its cyclic structure.
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.
e) galactose and fructose
b) has a downward projection in a Haworth projection.
In bacterial cell walls
a) polysaccharides form nonspecific mixtures with proteins
b) polysaccharides are hydrogen bonded together
c) peptides form crosslinks between polysaccharides
d) oligosaccharides form crosslinks between proteins
c) peptides form crosslinks between polysaccharides
The linkage between the glucose residues in amylopectin and glycogen is:
a) For the main chain α(1 → 4) and β(1 → 4) for the branches
b) For the main chain α(1 → 6) and α(1 → 4) for the branches
c) For the main chain α(1 → 4) and α(1 → 6) for the branches
d) For the main chain β(1 → 4) and β(1 → 6) for the branches
e) The linkage between the glucose residues is variable.
c) For the main chain α(1 → 4) and α(1 → 6) for the branches
Glycogen is
a) polysaccharide storage polymer found in plants
b) a linear polysaccharide
c) a highly branched polysaccharide found in animals
d) a synthetic sugar substitute
c) a highly branched polysaccharide found in animals
Which of the following monosaccharides is a ketose?
a. Glucose
b. Fructose
c. Galatose
d. Mannose
c. Fructose
How many carbon atoms are in the simplest carbohydrates?
a. 1
b. 2
c. 3
d. 4
e. 5
c. 3
The simplest aldotriose is:
a. acetone
b. dihydroxyacetone
c. glyceraldehyde
d. threose
c. glyceraldehyde
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. highest numbered asymmetric carbon atom
D-erythrose is to D-ribose as D-ribose is to:
a. D-allose
b. D-altrose
c. D-glucose
d. D-galactose
a. D-allose
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. epimers.
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. has one more chiral center (the anomeric carbon) than the open-chain form.
Which of the following groups is produced when an aldehyde is oxidized?
a. ketone
b.carboxyl
c. alcohol
d. ether
b.carboxyl
A lactone is a cyclic
a. ether.
b. ester.
c. ketone.
d. alcohol
b. ester.
Which of the following compounds is produced by oxidation of an aldose in the cyclic form?
a. a hemiacetal
b. hemiketal
c. lactone
d. amino sugar
c. lactone
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. Tollen’s reagent