Deck 25: Carbohydrates

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Question
What are the R/S stereochemical designations of C2 and C3 of L-threose? <strong>What are the R/S stereochemical designations of C2 and C3 of L-threose?  </strong> A)2R,3R B)2R,3S C)2S,3R D)2S,3S <div style=padding-top: 35px>

A)2R,3R
B)2R,3S
C)2S,3R
D)2S,3S
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Question
Which of the following is a disaccharide?

A)glucose
B)fructose
C)sucrose
D)mannitol
Question
What is (are) the major organic product(s) obtained from the following reaction? <strong>What is (are) the major organic product(s) obtained from the following reaction?  </strong> A)only 1 B)only 2 C)only 2 and 3 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 2 and 3
D)1, 2 and 3
Question
Which carbon in the following carbohydrate is the anomeric carbon? <strong>Which carbon in the following carbohydrate is the anomeric carbon?  </strong> A)i B)ii C)iii D)iv <div style=padding-top: 35px>

A)i
B)ii
C)iii
D)iv
Question
Which of the following structures represent the same carbohydrate? <strong>Which of the following structures represent the same carbohydrate?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)only 1 B)only 2 C)only 3 D)only 1 and 2 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 3
D)only 1 and 2
Question
Which carbon in the following carbohydrate is the anomeric carbon? <strong>Which carbon in the following carbohydrate is the anomeric carbon?  </strong> A)i B)ii C)iii D)iv <div style=padding-top: 35px>

A)i
B)ii
C)iii
D)iv
Question
What is the relationship between D-erythrose and D-threose? <strong>What is the relationship between D-erythrose and D-threose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers <div style=padding-top: 35px>

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
Question
What is the relationship between D-arabinose and L-arabinose? <strong>What is the relationship between D-arabinose and L-arabinose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers <div style=padding-top: 35px>

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
Question
Which of the following represents a pyranose? <strong>Which of the following represents a pyranose?  </strong> A)only 1 B)only 2 C)only 3 D)only 1 and 2 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 3
D)only 1 and 2
Question
Which of the following structures represent the same carbohydrate? <strong>Which of the following structures represent the same carbohydrate?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following represents a furanose? <strong>Which of the following represents a furanose?  </strong> A)only 1 B)only 2 C)only 3 D)only 2 and 3 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 3
D)only 2 and 3
Question
Which of the following has a D-configuration? <strong>Which of the following has a D-configuration?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)only 1, 2 and 3 <div style=padding-top: 35px>

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)only 1, 2 and 3
Question
What is the relationship between D-ribose and D-xylose? <strong>What is the relationship between D-ribose and D-xylose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers <div style=padding-top: 35px>

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
Question
Which of the following has a D-configuration? <strong>Which of the following has a D-configuration?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)only 1, 2 and 3 <div style=padding-top: 35px>

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)only 1, 2 and 3
Question
Which of the following represent a ketose? <strong>Which of the following represent a ketose?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
Question
What are the R/S stereochemical designations of C2 and C3 of D-erythrose? <strong>What are the R/S stereochemical designations of C2 and C3 of D-erythrose?  </strong> A)2R,3R B)2R,3S C)2S,3R D)2S,3S <div style=padding-top: 35px>

A)2R,3R
B)2R,3S
C)2S,3R
D)2S,3S
Question
Which of the following represent an aldose? <strong>Which of the following represent an aldose?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
Question
What is the relationship between D-threose and L-threose? <strong>What is the relationship between D-threose and L-threose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers <div style=padding-top: 35px>

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. Structure ____ represents a aldopentose.<div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
Structure ____ represents a aldopentose.
Question
Which of the following is vitamin C?

A)D-glucose
B)D-mannitol
C)L-ascorbic acid
D)L-sorbose
Question
Starch, cellulose, and surcrose are all classified as polysaccharides.
Question
Which of the following is not a polysaccharide?

A)amylose
B)amylopectin
C)glycogen
D)ribulose
Question
Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below). Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below).   The structure of D-erythrose is shown below.  <div style=padding-top: 35px> The structure of D-erythrose is shown below. Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below).   The structure of D-erythrose is shown below.  <div style=padding-top: 35px>
Question
Consider the following Fisher projections. Consider the following Fisher projections.   They all convert to the same tetrahedral representation as shown below..  <div style=padding-top: 35px> They all convert to the same tetrahedral representation as shown below.. Consider the following Fisher projections.   They all convert to the same tetrahedral representation as shown below..  <div style=padding-top: 35px>
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The formula for maltose is:   The number of the acetal carbon is _____.<div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
The formula for maltose is: Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The formula for maltose is:   The number of the acetal carbon is _____.<div style=padding-top: 35px> The number of the acetal carbon is _____.
Question
The following structure shows the correct assignment of the R or S configuration to each chirality center in sorbose. The following structure shows the correct assignment of the R or S configuration to each chirality center in sorbose.  <div style=padding-top: 35px>
Question
The following compound will react with Tollens' solution. The following compound will react with Tollens' solution.  <div style=padding-top: 35px>
Question
Reduction of an optically active aldopentose with NaBH4 gives an optically inactive alditol. The aldopentose could be: Reduction of an optically active aldopentose with NaBH<sub>4</sub> gives an optically inactive alditol. The aldopentose could be:  <div style=padding-top: 35px>
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The structures that represent reducing sugars are: a. only the ketoses. b. only the aldoses. c. all of these structures.<div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
The structures that represent reducing sugars are:
a. only the ketoses.
b. only the aldoses.
c. all of these structures.
Question
The following are two different methods of representing the same structure. The following are two different methods of representing the same structure.    <div style=padding-top: 35px> The following are two different methods of representing the same structure.    <div style=padding-top: 35px>
Question
A 1,4- α\alpha -linkage between two glucose units produces a disaccharide called maltose.
Question
Consider the structure shown below.  Consider the structure shown below.   The Haworth projection formula for the pyranose form of  \beta -D-galactose is given below.  <div style=padding-top: 35px>  The Haworth projection formula for the pyranose form of β\beta -D-galactose is given below.  Consider the structure shown below.   The Haworth projection formula for the pyranose form of  \beta -D-galactose is given below.  <div style=padding-top: 35px>
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. Structure ____ represents a ketohexose.<div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
Structure ____ represents a ketohexose.
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The number of hydroxyl groups in the pyranose form of glucose is _____.<div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
The number of hydroxyl groups in the pyranose form of glucose is _____.
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The number of the anomeric carbon in the following structure is _____.  <div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
The number of the anomeric carbon in the following structure is _____. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The number of the anomeric carbon in the following structure is _____.  <div style=padding-top: 35px>
Question
A glycoside is formed upon reaction of glucopyranose with NaBH4.
Question
The difference between the pyranose and furanose forms of a given aldohexose is the ring size.
Question
Which of the following is an alditol?

A)glucose
B)fructose
C)glucaric acid
D)mannitol
Question
What is the major organic product obtained from the following reduction of glucose? What is the major organic product obtained from the following reduction of glucose?  <div style=padding-top: 35px>
Question
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a sugar with three chirality centers.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
Question
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a deoxy sugar.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
Question
The textile rayon is produced by treatment of cellulose with carbon disulfide in aqueous sodium hydroxide. What type of functional group is introduced on the cellulose under these conditions? The textile rayon is produced by treatment of cellulose with carbon disulfide in aqueous sodium hydroxide. What type of functional group is introduced on the cellulose under these conditions?  <div style=padding-top: 35px>
Question
Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate. Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate.  <div style=padding-top: 35px>
Question
What are the major organic products obtained from treatment of a methyl glycoside with periodic acid in water? What are the major organic products obtained from treatment of a methyl glycoside with periodic acid in water?  <div style=padding-top: 35px>
Question
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a sugar which yields a single alditol upon reduction.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
Question
The textile cellulose acetate is produced by treatment of cellulose with acetic anhydride. What type of functional group is introduced on the cellulose under these conditions? The textile cellulose acetate is produced by treatment of cellulose with acetic anhydride. What type of functional group is introduced on the cellulose under these conditions?  <div style=padding-top: 35px>
Question
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The following monosaccharide has ________ equatorial hydroxyl groups.  <div style=padding-top: 35px> Answer the following questions by placing the appropriate number or indicated letter in the blank.
The following monosaccharide has ________ equatorial hydroxyl groups. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The following monosaccharide has ________ equatorial hydroxyl groups.  <div style=padding-top: 35px>
Question
Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate. Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate.  <div style=padding-top: 35px>
Question
Refer to the equilibrium below to answer the following question(s). Refer to the equilibrium below to answer the following question(s).    -The correct name for the cyclic structure is__________________________.<div style=padding-top: 35px>

-The correct name for the cyclic structure is__________________________.
Question
What is the major organic product obtained from the reaction of glucose with glucose oxidase? What is the major organic product obtained from the reaction of glucose with glucose oxidase?  <div style=padding-top: 35px>
Question
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a D-sugar.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)  <div style=padding-top: 35px>
Question
Refer to the equilibrium below to answer the following question(s). Refer to the equilibrium below to answer the following question(s).   The enantiomer of ribose is drawn is _______. (D or L)<div style=padding-top: 35px>
The enantiomer of ribose is drawn is _______. (D or L)
Question
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
The fundamental difference between the monosaccharide, disaccharide, and polysaccharide classifications of carbohydrates is the number of _________________present.
Question
Refer to the equilibrium below to answer the following question(s). Refer to the equilibrium below to answer the following question(s).    -The anomer of ribose is drawn is _______. (alpha or beta)<div style=padding-top: 35px>

-The anomer of ribose is drawn is _______. (alpha or beta)
Question
What are the major organic products obtained from treatment of a 1,2,3-triol with periodic acid in water? What are the major organic products obtained from treatment of a 1,2,3-triol with periodic acid in water?  <div style=padding-top: 35px>
Question
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
The name of the following Fischer projection including stereochemistry is _____________________. From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. The name of the following Fischer projection including stereochemistry is _____________________.  <div style=padding-top: 35px>
Question
What are the two major organic products obtained from treatment of an α\alpha
-hydroxyketone with periodic acid in water?  What are the two major organic products obtained from treatment of an  \alpha  -hydroxyketone with periodic acid in water?  <div style=padding-top: 35px>
Question
What are the two major organic products obtained from the following reaction? What is the relationship between them? (What type of isomers are they?) What are the two major organic products obtained from the following reaction? What is the relationship between them? (What type of isomers are they?)  <div style=padding-top: 35px>
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Deck 25: Carbohydrates
1
What are the R/S stereochemical designations of C2 and C3 of L-threose? <strong>What are the R/S stereochemical designations of C2 and C3 of L-threose?  </strong> A)2R,3R B)2R,3S C)2S,3R D)2S,3S

A)2R,3R
B)2R,3S
C)2S,3R
D)2S,3S
2R,3S
2
Which of the following is a disaccharide?

A)glucose
B)fructose
C)sucrose
D)mannitol
sucrose
3
What is (are) the major organic product(s) obtained from the following reaction? <strong>What is (are) the major organic product(s) obtained from the following reaction?  </strong> A)only 1 B)only 2 C)only 2 and 3 D)1, 2 and 3

A)only 1
B)only 2
C)only 2 and 3
D)1, 2 and 3
only 2 and 3
4
Which carbon in the following carbohydrate is the anomeric carbon? <strong>Which carbon in the following carbohydrate is the anomeric carbon?  </strong> A)i B)ii C)iii D)iv

A)i
B)ii
C)iii
D)iv
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5
Which of the following structures represent the same carbohydrate? <strong>Which of the following structures represent the same carbohydrate?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
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6
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)only 1 B)only 2 C)only 3 D)only 1 and 2

A)only 1
B)only 2
C)only 3
D)only 1 and 2
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7
Which carbon in the following carbohydrate is the anomeric carbon? <strong>Which carbon in the following carbohydrate is the anomeric carbon?  </strong> A)i B)ii C)iii D)iv

A)i
B)ii
C)iii
D)iv
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8
What is the relationship between D-erythrose and D-threose? <strong>What is the relationship between D-erythrose and D-threose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
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9
What is the relationship between D-arabinose and L-arabinose? <strong>What is the relationship between D-arabinose and L-arabinose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
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10
Which of the following represents a pyranose? <strong>Which of the following represents a pyranose?  </strong> A)only 1 B)only 2 C)only 3 D)only 1 and 2

A)only 1
B)only 2
C)only 3
D)only 1 and 2
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11
Which of the following structures represent the same carbohydrate? <strong>Which of the following structures represent the same carbohydrate?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
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12
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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13
Which of the following represents a furanose? <strong>Which of the following represents a furanose?  </strong> A)only 1 B)only 2 C)only 3 D)only 2 and 3

A)only 1
B)only 2
C)only 3
D)only 2 and 3
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14
Which of the following has a D-configuration? <strong>Which of the following has a D-configuration?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)only 1, 2 and 3

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)only 1, 2 and 3
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15
What is the relationship between D-ribose and D-xylose? <strong>What is the relationship between D-ribose and D-xylose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
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16
Which of the following has a D-configuration? <strong>Which of the following has a D-configuration?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)only 1, 2 and 3

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)only 1, 2 and 3
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17
Which of the following represent a ketose? <strong>Which of the following represent a ketose?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
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18
What are the R/S stereochemical designations of C2 and C3 of D-erythrose? <strong>What are the R/S stereochemical designations of C2 and C3 of D-erythrose?  </strong> A)2R,3R B)2R,3S C)2S,3R D)2S,3S

A)2R,3R
B)2R,3S
C)2S,3R
D)2S,3S
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19
Which of the following represent an aldose? <strong>Which of the following represent an aldose?  </strong> A)only 1 and 2 B)only 1 and 3 C)only 2 and 3 D)1, 2 and 3

A)only 1 and 2
B)only 1 and 3
C)only 2 and 3
D)1, 2 and 3
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20
What is the relationship between D-threose and L-threose? <strong>What is the relationship between D-threose and L-threose?  </strong> A)constitutional isomers B)enantiomers C)diastereomers D)tautomers

A)constitutional isomers
B)enantiomers
C)diastereomers
D)tautomers
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21
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. Structure ____ represents a aldopentose. Answer the following questions by placing the appropriate number or indicated letter in the blank.
Structure ____ represents a aldopentose.
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22
Which of the following is vitamin C?

A)D-glucose
B)D-mannitol
C)L-ascorbic acid
D)L-sorbose
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23
Starch, cellulose, and surcrose are all classified as polysaccharides.
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24
Which of the following is not a polysaccharide?

A)amylose
B)amylopectin
C)glycogen
D)ribulose
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25
Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below). Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below).   The structure of D-erythrose is shown below.  The structure of D-erythrose is shown below. Oxidation of optically active D-erythrose with nitric acid produces optically inactive meso-tartaric acid (below).   The structure of D-erythrose is shown below.
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26
Consider the following Fisher projections. Consider the following Fisher projections.   They all convert to the same tetrahedral representation as shown below..  They all convert to the same tetrahedral representation as shown below.. Consider the following Fisher projections.   They all convert to the same tetrahedral representation as shown below..
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27
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The formula for maltose is:   The number of the acetal carbon is _____. Answer the following questions by placing the appropriate number or indicated letter in the blank.
The formula for maltose is: Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The formula for maltose is:   The number of the acetal carbon is _____. The number of the acetal carbon is _____.
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28
The following structure shows the correct assignment of the R or S configuration to each chirality center in sorbose. The following structure shows the correct assignment of the R or S configuration to each chirality center in sorbose.
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29
The following compound will react with Tollens' solution. The following compound will react with Tollens' solution.
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30
Reduction of an optically active aldopentose with NaBH4 gives an optically inactive alditol. The aldopentose could be: Reduction of an optically active aldopentose with NaBH<sub>4</sub> gives an optically inactive alditol. The aldopentose could be:
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31
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The structures that represent reducing sugars are: a. only the ketoses. b. only the aldoses. c. all of these structures. Answer the following questions by placing the appropriate number or indicated letter in the blank.
The structures that represent reducing sugars are:
a. only the ketoses.
b. only the aldoses.
c. all of these structures.
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32
The following are two different methods of representing the same structure. The following are two different methods of representing the same structure.    The following are two different methods of representing the same structure.
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33
A 1,4- α\alpha -linkage between two glucose units produces a disaccharide called maltose.
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34
Consider the structure shown below.  Consider the structure shown below.   The Haworth projection formula for the pyranose form of  \beta -D-galactose is given below.   The Haworth projection formula for the pyranose form of β\beta -D-galactose is given below.  Consider the structure shown below.   The Haworth projection formula for the pyranose form of  \beta -D-galactose is given below.
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35
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. Structure ____ represents a ketohexose. Answer the following questions by placing the appropriate number or indicated letter in the blank.
Structure ____ represents a ketohexose.
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36
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The number of hydroxyl groups in the pyranose form of glucose is _____. Answer the following questions by placing the appropriate number or indicated letter in the blank.
The number of hydroxyl groups in the pyranose form of glucose is _____.
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37
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The number of the anomeric carbon in the following structure is _____.  Answer the following questions by placing the appropriate number or indicated letter in the blank.
The number of the anomeric carbon in the following structure is _____. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The number of the anomeric carbon in the following structure is _____.
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38
A glycoside is formed upon reaction of glucopyranose with NaBH4.
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39
The difference between the pyranose and furanose forms of a given aldohexose is the ring size.
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40
Which of the following is an alditol?

A)glucose
B)fructose
C)glucaric acid
D)mannitol
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41
What is the major organic product obtained from the following reduction of glucose? What is the major organic product obtained from the following reduction of glucose?
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42
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a sugar with three chirality centers.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar with three chirality centers.</strong> A)  B)  C)  D)
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43
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a deoxy sugar.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a deoxy sugar.</strong> A)  B)  C)  D)
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44
The textile rayon is produced by treatment of cellulose with carbon disulfide in aqueous sodium hydroxide. What type of functional group is introduced on the cellulose under these conditions? The textile rayon is produced by treatment of cellulose with carbon disulfide in aqueous sodium hydroxide. What type of functional group is introduced on the cellulose under these conditions?
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45
Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate. Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate.
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46
What are the major organic products obtained from treatment of a methyl glycoside with periodic acid in water? What are the major organic products obtained from treatment of a methyl glycoside with periodic acid in water?
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47
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a sugar which yields a single alditol upon reduction.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a sugar which yields a single alditol upon reduction.</strong> A)  B)  C)  D)
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48
The textile cellulose acetate is produced by treatment of cellulose with acetic anhydride. What type of functional group is introduced on the cellulose under these conditions? The textile cellulose acetate is produced by treatment of cellulose with acetic anhydride. What type of functional group is introduced on the cellulose under these conditions?
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49
Consider the following structures. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The following monosaccharide has ________ equatorial hydroxyl groups.  Answer the following questions by placing the appropriate number or indicated letter in the blank.
The following monosaccharide has ________ equatorial hydroxyl groups. Consider the following structures.   Answer the following questions by placing the appropriate number or indicated letter in the blank. The following monosaccharide has ________ equatorial hydroxyl groups.
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50
Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate. Complete the structure on the right so that it represents the pyranose form of the carbohydrate shown on the left as a Fischer projection. Place the substituents carefully so that their position in axial or equatorial positions accurately reflects the stereochemistry of the carbohydrate.
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51
Refer to the equilibrium below to answer the following question(s). Refer to the equilibrium below to answer the following question(s).    -The correct name for the cyclic structure is__________________________.

-The correct name for the cyclic structure is__________________________.
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52
What is the major organic product obtained from the reaction of glucose with glucose oxidase? What is the major organic product obtained from the reaction of glucose with glucose oxidase?
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53
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
_____ is a D-sugar.

A)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)
B)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)
C)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)
D)<strong>From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. _____ is a D-sugar.</strong> A)  B)  C)  D)
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54
Refer to the equilibrium below to answer the following question(s). Refer to the equilibrium below to answer the following question(s).   The enantiomer of ribose is drawn is _______. (D or L)
The enantiomer of ribose is drawn is _______. (D or L)
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55
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
The fundamental difference between the monosaccharide, disaccharide, and polysaccharide classifications of carbohydrates is the number of _________________present.
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56
Refer to the equilibrium below to answer the following question(s). Refer to the equilibrium below to answer the following question(s).    -The anomer of ribose is drawn is _______. (alpha or beta)

-The anomer of ribose is drawn is _______. (alpha or beta)
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57
What are the major organic products obtained from treatment of a 1,2,3-triol with periodic acid in water? What are the major organic products obtained from treatment of a 1,2,3-triol with periodic acid in water?
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58
From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question.
The name of the following Fischer projection including stereochemistry is _____________________. From the sugars below, choose the one that best fits each description below. Place the letter of the sugar in the blank to the left of the description. There is only one correct answer for each question. The name of the following Fischer projection including stereochemistry is _____________________.
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59
What are the two major organic products obtained from treatment of an α\alpha
-hydroxyketone with periodic acid in water?  What are the two major organic products obtained from treatment of an  \alpha  -hydroxyketone with periodic acid in water?
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60
What are the two major organic products obtained from the following reaction? What is the relationship between them? (What type of isomers are they?) What are the two major organic products obtained from the following reaction? What is the relationship between them? (What type of isomers are they?)
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