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Predict the product(s) for the following Wohl degradation. Predict the product(s)  for the following Wohl degradation.     A)  I B)  II C)  III D)  IV E)  V Predict the product(s)  for the following Wohl degradation.     A)  I B)  II C)  III D)  IV E)  V


A) I
B) II
C) III
D) IV
E) V

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

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Which of the following is a D-aldopentose? Which of the following is a D-aldopentose?   A)  I B)  II C)  III D)  IV E)  I and V


A) I
B) II
C) III
D) IV
E) I and V

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

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Predict the product(s) for the following reaction. Predict the product(s)  for the following reaction.       A)  I B)  I and II C)  III and IV D)  IV E)  I, II and IV Predict the product(s)  for the following reaction.       A)  I B)  I and II C)  III and IV D)  IV E)  I, II and IV Predict the product(s)  for the following reaction.       A)  I B)  I and II C)  III and IV D)  IV E)  I, II and IV


A) I
B) I and II
C) III and IV
D) IV
E) I, II and IV

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

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Which of the following compound(s) is a glycoside? Which of the following compound(s)  is a glycoside?     A)  I B)  II C)  II and III D)  III and IV E)  II, III and IV Which of the following compound(s)  is a glycoside?     A)  I B)  II C)  II and III D)  III and IV E)  II, III and IV


A) I
B) II
C) II and III
D) III and IV
E) II, III and IV

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

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Draw a Fisher projection for the enantiomer of D-glucose.

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Which of the following best describes the relationship between D-glucose and D-fructose?


A) enantiomers
B) epimers
C) anomers
D) constitutional isomers
E) diastereomers

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

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Identify the compound that is found in nature.


A) D-(+) -glyceraldehyde
B) L-(+) -glyceraldehyde
C) D-(-) -glyceraldehyde
D) L-(-) -glyceraldehyde
E) none of these

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

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Which of the following compound(s) would undergo mutarotation in aqueous solution? Which of the following compound(s)  would undergo mutarotation in aqueous solution?     A)  I B)  II and III C)  III and IV D)  I, II, and III E)  all of these Which of the following compound(s)  would undergo mutarotation in aqueous solution?     A)  I B)  II and III C)  III and IV D)  I, II, and III E)  all of these


A) I
B) II and III
C) III and IV
D) I, II, and III
E) all of these

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

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Draw a Fisher projection for D-fructose.

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Simple sugars are called_______ , a term that derives from the Latin word for sugar, saccharum.


A) monosaccharides
B) disaccharides
C) polysaccharides
D) saccharides
E) all of these

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

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In the Fischer projection of D-glyceraldehyde the OH group connected to the chirality center farthest from the carbonyl group is pointing _______.


A) to the left
B) to the right
C) up
D) down
E) all of these

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

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Provide the reagents necessary to carry out the following conversion. Provide the reagents necessary to carry out the following conversion.

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Predict the product(s) for the following reaction. Predict the product(s) for the following reaction.

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Identify the monosaccharide(s) in β\beta -lactose.

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blured image-D-galacto...

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Which of the following is a ketopentose? Which of the following is a ketopentose?   A)  D-lyxose B)  D-fructose C)  D-ribose D)  D-glucose E)  D-xylulose


A) D-lyxose
B) D-fructose
C) D-ribose
D) D-glucose
E) D-xylulose

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

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What is the correct name for the following compound?  What is the correct name for the following compound?   A)  ( \alpha -D-glucopyranose)  B)  ( \alpha -D-allopyranose)  C)  ( \beta -D-glucopyranose)  D)  ( \alpha -D-galactopyranose)  E)  ( \beta -D-gulopyranose)


A) ( α\alpha -D-glucopyranose)
B) ( α\alpha -D-allopyranose)
C) ( β\beta -D-glucopyranose)
D) ( α\alpha -D-galactopyranose)
E) ( β\beta -D-gulopyranose)

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

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Predict the product(s) for the following reaction. Predict the product(s)  for the following reaction.     A)  I B)  II C)  III D)  IV E)  V Predict the product(s)  for the following reaction.     A)  I B)  II C)  III D)  IV E)  V


A) I
B) II
C) III
D) IV
E) V

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

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Which of the following would reduce a Fehling solution?


A) maltose
B) cellobiose
C) sucrose
D) lactose
E) A, B and D

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

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Which of the following compounds would produce D-glucose and D-mannose when treated with HCN followed by H2/Pd/BaSO4/H2O? Which of the following compounds would produce D-glucose and D-mannose when treated with HCN followed by H<sub>2</sub>/Pd/BaSO<sub>4</sub>/H<sub>2</sub>O?   A)  I B)  II C)  III D)  IV E)  V


A) I
B) II
C) III
D) IV
E) V

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

Correct Answer

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Which of the following structures represent β\beta -D-glucopyranose?  Which of the following structures represent  \beta -D-glucopyranose?     A)  I B)  II C)  III D)  IV E)  none of these  Which of the following structures represent  \beta -D-glucopyranose?     A)  I B)  II C)  III D)  IV E)  none of these


A) I
B) II
C) III
D) IV
E) none of these

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

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