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A monosaccharide that contains 4 carbon atoms, one of which is in an aldehyde group, is classified as a(n)


A) aldopentose.
B) aldohexose.
C) aldotetrose.
D) ketopentose.
E) ketotetrose.

F) All of the above
G) A) and C)

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One difference between D-glucose and L-glucose is


A) L-glucose cannot form a closed structure.
B) L-glucose has a 5-membered ring, and D-glucose has a 6-membered ring.
C) the open-chain form of L-glucose does not exist.
D) it is not possible to make L-glucose.
E) only D-glucose is more commonly found in disaccharides and polysaccharides.

F) A) and B)
G) B) and E)

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Which sugar is NOT a reducing sugar?


A) glucose
B) galactose
C) sucrose
D) fructose
E) maltose

F) B) and D)
G) None of the above

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In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written


A) on the left of the bottom chiral carbon.
B) on the right of the top chiral carbon.
C) on the left of the middle chiral carbon.
D) on the right of the bottom chiral carbon.
E) on the left of the top chiral carbon.

F) B) and C)
G) A) and E)

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Photosynthesis uses ________ as an energy source.


A) sunlight
B) glucose
C) oxygen
D) carbon dioxide
E) chlorophyll

F) D) and E)
G) B) and D)

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Identify each Fischer projection as the D- or L-isomer. -Identify each Fischer projection as the D- or L-isomer. -

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Hypoglycemia is a condition in which


A) the glucose level in the blood is higher than normal.
B) the amount of glucose in the urine is higher than normal.
C) the glucose level in the pancreas is higher than normal.
D) the glucose level in the blood is lower than normal.
E) the glucose level in the blood is about 100 mg/dL.

F) A) and E)
G) B) and E)

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Galactose is one of the products of enzymatic hydrolysis of


A) sucrose.
B) lactose.
C) glucose.
D) maltose.
E) erythrose.

F) B) and D)
G) B) and E)

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A carbohydrate that gives two molecules when it is completely hydrolyzed is known as a


A) polysaccharide.
B) monosaccharide.
C) starch.
D) trisaccharide.
E) disaccharide.

F) B) and E)
G) C) and D)

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Which group of carbohydrates cannot be hydrolyzed to give smaller molecules?


A) oligosaccharides
B) trisaccharides
C) disaccharides
D) monosaccharides
E) polysaccharides

F) A) and B)
G) A) and C)

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Which of the following is an example of an aldohexose?


A) Which of the following is an example of an aldohexose? A)    B)    C)    D)    E)
B) Which of the following is an example of an aldohexose? A)    B)    C)    D)    E)
C) Which of the following is an example of an aldohexose? A)    B)    C)    D)    E)
D) Which of the following is an example of an aldohexose? A)    B)    C)    D)    E)
E) Which of the following is an example of an aldohexose? A)    B)    C)    D)    E)

F) None of the above
G) A) and E)

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Under acid hydrolysis conditions, starch is ultimately converted to


A) fructose.
B) galactose.
C) xylose.
D) maltose.
E) glucose.

F) B) and E)
G) A) and E)

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Which molecule below has stereoisomers with different biological effects?


A) carvone
B) naproxen
C) epinephrine
D) nicotine
E) All of the above.

F) B) and D)
G) B) and C)

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The reduction of monosaccharides produces


A) disaccharides.
B) sugar acids.
C) polysaccharides.
D) trisaccharides.
E) sugar alcohols.

F) D) and E)
G) C) and D)

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Amylose is a polysaccharide which has


A) only Amylose is a polysaccharide which has A)  only   bonds glucose units. B)  hemiacetal links joining glucose units. C)  carbon-carbon bonds joining glucose units. D)  both   bonds between glucose units. E)  only   bonds between glucose units. bonds glucose units.
B) hemiacetal links joining glucose units.
C) carbon-carbon bonds joining glucose units.
D) both Amylose is a polysaccharide which has A)  only   bonds glucose units. B)  hemiacetal links joining glucose units. C)  carbon-carbon bonds joining glucose units. D)  both   bonds between glucose units. E)  only   bonds between glucose units. bonds between glucose units.
E) only Amylose is a polysaccharide which has A)  only   bonds glucose units. B)  hemiacetal links joining glucose units. C)  carbon-carbon bonds joining glucose units. D)  both   bonds between glucose units. E)  only   bonds between glucose units. bonds between glucose units.

F) A) and E)
G) None of the above

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Which of the following is an example of a ketopentose?


A) Which of the following is an example of a ketopentose?  A)    B)    C)    D)    E)
B) Which of the following is an example of a ketopentose?  A)    B)    C)    D)    E)
C) Which of the following is an example of a ketopentose?  A)    B)    C)    D)    E)
D) Which of the following is an example of a ketopentose?  A)    B)    C)    D)    E)
E) Which of the following is an example of a ketopentose?  A)    B)    C)    D)    E)

F) A) and C)
G) D) and E)

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Refer to the disaccharides below to answer the question(s) that follow. Refer to the disaccharides below to answer the question(s) that follow.   -Hydrolysis of the disaccharide above gives the monosaccharides A) ribose and glucose. B) fructose and lactose. C) fructose and ribose. D) fructose and glucose. E) ribose and galactose. -Hydrolysis of the disaccharide above gives the monosaccharides


A) ribose and glucose.
B) fructose and lactose.
C) fructose and ribose.
D) fructose and glucose.
E) ribose and galactose.

F) A) and D)
G) A) and B)

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Chiral drugs consist of only one enantiomer. The benefits of using a pure enantiomer, rather than a mixture, include


A) reduced chances of drug interactions.
B) elimination of side effects.
C) higher potency (lower total dose of drug) .
D) All of the above.
E) None of the above.

F) A) and B)
G) A) and E)

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Fructose does not undergo hydrolysis because it is a(n)


A) aldose.
B) disaccharide.
C) hexose.
D) monosaccharide.
E) reducing sugar.

F) All of the above
G) B) and C)

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The sugar also known as dextrose and blood sugar is


A) lactose.
B) sucrose.
C) glucose.
D) galactose.
E) fructose.

F) A) and E)
G) B) and E)

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