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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?   A)  1 B)  2 C)  3 D)  4


A) 1
B) 2
C) 3
D) 4

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

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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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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. 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. -_____ is a D-sugar.

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What is (are) the major organic product(s) obtained from the following reaction? What is (are)  the major organic product(s)  obtained from the following reaction?   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

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

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Match the following compounds used to produce rayon and acetate rayon with the most appropriate roles. -Causes fibers to dissolve in an alkali


A) Sodium salt of xanthate ester
B) Acetylated cellulose
C) Carbon disulfide
D) Dilute sulfuric acid

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

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A

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:

A) True
B) False

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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. 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. -_____ is a deoxy sugar.

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Which of the following is not a polysaccharide?


A) amylose
B) amylopectin
C) glycogen
D) ribulose

E) C) and D)
F) All of the above

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The following monosaccharide has ________ equatorial hydroxyl groups. The following monosaccharide has ________ equatorial hydroxyl groups.

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Identify the given compound. ​ Identify the given compound. ​   A)  β lactose B)  β maltose C)  α sucrose D)  α maltose


A) β lactose
B) β maltose
C) α sucrose
D) α maltose

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

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A

Consider the structure shown below. Consider the structure shown below.   The Haworth projection formula for the pyranose form of β-D-galactose is given below.  The Haworth projection formula for the pyranose form of β-D-galactose is given below. Consider the structure shown below.   The Haworth projection formula for the pyranose form of β-D-galactose is given below.

A) True
B) False

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What is the relationship between D-erythrose and D-threose? What is the relationship between D-erythrose and D-threose?   A)  constitutional isomers B)  enantiomers C)  diastereomers D)  tautomers


A) constitutional isomers
B) enantiomers
C) diastereomers
D) tautomers

E) A) and D)
F) B) and C)

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Which carbon in the following carbohydrate is the anomeric carbon? Which carbon in the following carbohydrate is the anomeric carbon?   A)  i B)  ii C)  iii D)  iv


A) i
B) ii
C) iii
D) iv

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

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


A) constitutional isomers
B) enantiomers
C) diastereomers
D) tautomers

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

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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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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. 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. -_____ is a sugar which yields a single alditol upon reduction.

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b

The formula for maltose is: The formula for maltose is:   The number of the acetal carbon is _____. The number of the acetal carbon is _____.

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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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What are the R/S stereochemical designations of C2 and C3 of D-erythrose? What are the R/S stereochemical designations of C2 and C3 of D-erythrose?   A)  2R,3R B)  2R,3S C)  2S,3R D)  2S,3S


A) 2R,3R
B) 2R,3S
C) 2S,3R
D) 2S,3S

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

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A glycoside is formed upon reaction of glucopyranose with NaBH4.

A) True
B) False

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