Deck 20: Carbohydrates

Full screen (f)
exit full mode
Question
What product forms when the compound below is treated with H2 in the presence of a Pd catalyst? <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Use Space or
up arrow
down arrow
to flip the card.
Question
When converting a Fischer projection to a Haworth projection,where are all of the substituents on the right side of the carbon skeleton drawn in the Haworth projection?

A)Down
B)Up
C)Down in an α anomer and up in a β anomer
D)Down in an β anomer and up in a α anomer
Question
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)Aldohexose B)Aldopentose C)Ketotetrose D)Ketopentose <div style=padding-top: 35px>

A)Aldohexose
B)Aldopentose
C)Ketotetrose
D)Ketopentose
Question
What are monosaccharides with a carbonyl group at C1 called?

A)Anomers
B)Aldoses
C)Ketoses
D)Alditols
Question
Which carbohydrates cannot be converted to simpler compounds by hydrolysis?

A)Disaccharides
B)Monosaccharides
C)Polysaccharides
D)Starches
Question
Which monosaccharide is an aldotriose?

A) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
In the monosaccharide given,which of the labeled carbons are chiral centers? <strong>In the monosaccharide given,which of the labeled carbons are chiral centers?  </strong> A)C<sub>1 </sub>is the only chiral center. B)C<sub>1</sub> and C<sub>2</sub> are both chiral centers. C)C<sub>2</sub> and C<sub>3</sub> are both chiral centers D)C<sub>3</sub> is the only chiral center <div style=padding-top: 35px>

A)C1 is the only chiral center.
B)C1 and C2 are both chiral centers.
C)C2 and C3 are both chiral centers
D)C3 is the only chiral center
Question
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)An aldohexose B)A ketohexose C)An aldopentose D)A ketopentose <div style=padding-top: 35px>

A)An aldohexose
B)A ketohexose
C)An aldopentose
D)A ketopentose
Question
How many chirality centers are present in the compound shown below? <strong>How many chirality centers are present in the compound shown below?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
How many chirality centers are present in the compound shown below? <strong>How many chirality centers are present in the compound shown below?  </strong> A)2 B)4 C)5 D)6 <div style=padding-top: 35px>

A)2
B)4
C)5
D)6
Question
Which Haworth projection represents the banomer of the monosaccharide shown below? <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Which of the following is a ketohexose?

A) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What is the classification of the monosaccharide shown? <strong>What is the classification of the monosaccharide shown?  </strong> A)L B)D C)A sugar this large is not classified as L or D. <div style=padding-top: 35px>

A)L
B)D
C)A sugar this large is not classified as L or D.
Question
Which compound is the most soluble in water?

A)CH2OHCHOHCHOHCHOHCHOHCHO
B)CH3CH2CH=CHCH2CH=CHCH2CH2CH2CH2CH2CH2CH2COOH
C)CH3CH2CH2CH2CH2CH2CH2CH2CH3
D)CH3CH2CH2CH2CH2CH2CH2CH2OH
Question
Which labeled carbon atom in the structure below is the anomeric carbon? <strong>Which labeled carbon atom in the structure below is the anomeric carbon?  </strong> A)A B)B C)C D)D <div style=padding-top: 35px>

A)A
B)B
C)C
D)D
Question
Which Haworth projection represents the α anomer of the monosaccharide shown below? <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The structures of galactose (left)and glucose (right)are shown below. How are the two monosaccharides related? <strong>The structures of galactose (left)and glucose (right)are shown below. How are the two monosaccharides related?  </strong> A)Structural isomers B)Stereoisomers C)Enantiomers D)Anomers <div style=padding-top: 35px>

A)Structural isomers
B)Stereoisomers
C)Enantiomers
D)Anomers
Question
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)A tetraketose B)A ketotriose C)A ketotetrose D)An aldotriose <div style=padding-top: 35px>

A)A tetraketose
B)A ketotriose
C)A ketotetrose
D)An aldotriose
Question
The formation of what color in the Benedict's test indicates a reducing sugar is present in solution?

A)Blue
B)Brick red
C)Bright yellow
D)Silver
Question
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)L B)D C)A sugar this small is not classified as L or D. <div style=padding-top: 35px>

A)L
B)D
C)A sugar this small is not classified as L or D.
Question
Which is the only polysaccharide to have β-glycosidic bonds?

A)Glycogen
B)Amylose
C)Cellulose
D)Amylopectin
Question
What is the most common type of starch molecules?

A)Cellulose
B)Amylose
C)Amylopectin
D)Glycogen
Question
Which choice properly describes the glycoside bond in the disaccharide below? <strong>Which choice properly describes the glycoside bond in the disaccharide below?  </strong> A)1→6-α B)1→6-β C)1→4α D)1→4β <div style=padding-top: 35px>

A)1→6-α
B)1→6-β
C)1→4α
D)1→4β
Question
What product forms when the compound below is treated with Benedict's reagent? <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
How many acetals and hemiacetals are present in the disaccharide below? <strong>How many acetals and hemiacetals are present in the disaccharide below?  </strong> A)Two acetals are present. B)Two hemiacetals are present. C)One hemiacetal and one acetal is present D)No hemiacetals or acetals are present. <div style=padding-top: 35px>

A)Two acetals are present.
B)Two hemiacetals are present.
C)One hemiacetal and one acetal is present
D)No hemiacetals or acetals are present.
Question
What is responsible for the different blood types in humans?

A)Three or four proteins attached to a membrane monosaccharide on the surface of red blood cells
B)Three or four monosaccharides attached to a membrane protein on the surface of red blood cells
C)Three or four amino acids attached to a membrane monosaccharide on the surface of red blood cells
D)Three or four lipids attached to a membrane polysaccharide on the surface of red blood cells
Question
Which is not a naturally-occurring polysaccharide?

A)Starch
B)Cellulose
C)Maltose
D)Glycogen
Question
Which is not a glycosaminoglycan?

A)Hyaluronate
B)Chitin
C)Heparin
D)Chondroitin
Question
Which carbohydrate derivative forms a gel-like matrix in joints and the vitreous humor of the eye?

A)Heparin
B)Chondroitin
C)Hyaluronate
D)Chitin
Question
What is the structure of amylopectin?

A)Unbranched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
B)Branched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
C)Unbranched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
D)Branched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
Question
Chitin is identical in structure to cellulose,except that

A)The linkages are a-glycoside linkages.
B)Each OH group at C4 is replaced by NHCOCH3.
C)Each OH group at C2 is replaced by NH3.
D)Each OH group at C2 is replaced by NHCOCH3.
Question
What product forms when the compound below is treated with Benedict's reagent? <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs. <div style=padding-top: 35px>

A) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs. <div style=padding-top: 35px>
B) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs. <div style=padding-top: 35px>
C) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs. <div style=padding-top: 35px>
D) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs. <div style=padding-top: 35px>
E)No reaction occurs.
Question
Salicin is a naturally occurring,carbohydrate-containing pain reliever. Which statement concerning the functional groups present in salicin is incorrect? <strong>Salicin is a naturally occurring,carbohydrate-containing pain reliever. Which statement concerning the functional groups present in salicin is incorrect?  </strong> A)Salicin contains an acetal. B)Salicin contains an alcohol. C)Salicin contains a hemiacetal. D)Salicin contains a phenol. <div style=padding-top: 35px>

A)Salicin contains an acetal.
B)Salicin contains an alcohol.
C)Salicin contains a hemiacetal.
D)Salicin contains a phenol.
Question
What is the structure of cellulose?

A)Unbranched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
B)Branched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
C)Unbranched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
D)Branched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
Question
Why are humans not able to digest cellulose?

A)Humans cannot digest glucose.
B)Humans do not possess the enzyme necessary to hydrolyze the 1→4-β-glycoside linkages found in cellulose.
C)Humans do not possess the enzyme necessary to unwind the helical shape of the cellulose molecule.
D)Humans do not possess the enzyme necessary to hydrolyze the 1→4-α-glycoside linkages found in cellulose.
Question
Disaccharides and polysaccharides contain monosaccharide units joined together by which of the following?

A)Hydrogen bonding
B)Glycosidic linkages
C)Hemiacetal bonds
D)Dipole-dipole forces
Question
What is the polysaccharide form in which glucose is stored in animals?

A)Cellulose
B)Amylose
C)Amylopectin
D)Glycogen
Question
How many acetals are present in the disaccharide shown below? <strong>How many acetals are present in the disaccharide shown below?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Lactose is present in milk. What type of sugar is lactose?

A)A disaccharide
B)A monosaccharide
C)A polysaccharide
D)A starch
Question
What monosaccharide is found in cellulose,starch,and glycogen?

A)Glucose
B)Galactose
C)Sucrose
D)Fructose
Question
Dihydroxyacetone,shown below,is the simplest ketose. Does the structure shown represent D-dihydroxyacetone or L-dihydroxyacetone? <strong>Dihydroxyacetone,shown below,is the simplest ketose. Does the structure shown represent D-dihydroxyacetone or L-dihydroxyacetone?  </strong> A)D-dihydroxyacetone B)L-dihydroxyacetone C)Neither D nor L; dihydroxyacetone is not chiral D)It is impossible to tell from the Fischer projection alone. <div style=padding-top: 35px>

A)D-dihydroxyacetone
B)L-dihydroxyacetone
C)Neither D nor L; dihydroxyacetone is not chiral
D)It is impossible to tell from the Fischer projection alone.
Question
Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product? <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The monosaccharide shown below is an α anomer. The monosaccharide shown below is an α anomer.  <div style=padding-top: 35px>
Question
At equilibrium,a solution of glucose in water is an equal mixture of the α anomer,the β anomer,and the acyclic aldehyde.
Question
When a monosaccharide forms a cyclic hemiacetal,the carbon atom that is part of the hemiacetal is a new chirality center,called the anomeric carbon.
Question
The β anomer of a cyclic monosaccharide has the -OH group drawn down,below the ring.
Question
The Fischer projections of two monosaccharides are shown below. Which term best describes the relationship between the two? <strong>The Fischer projections of two monosaccharides are shown below. Which term best describes the relationship between the two?  </strong> A)Enantiomers B)Anomers C)Constitutional isomers D)Diastereomers <div style=padding-top: 35px>

A)Enantiomers
B)Anomers
C)Constitutional isomers
D)Diastereomers
Question
Which statement concerning carbohydrates is incorrect?

A)Carbohydrates serve important energy and structural roles for both plants and animals.
B)Monosaccharides are the simplest carbohydrates and are known as simple sugars.
C)Humans store excess glucose for short term energy requirements in the polysaccharide cellulose.
D)Carbohydrates that can be oxidized by Benedict's reagent are called reducing sugars.
Question
A hemiacetal is a compound that contains a hydroxyl group (-OH)and an alkoxy group (-OR)on adjacent carbon atoms.
Question
The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?

A) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Certain monosaccharides-notably aldopentoses and ketohexoses-form five-membered rings,not six-membered rings,in solution.
Question
Melibiose is a carbohydrate found in some plant juices. Which statement concerning melibiose is incorrect? <strong>Melibiose is a carbohydrate found in some plant juices. Which statement concerning melibiose is incorrect?  </strong> A)It is a disaccharide. B)It is composed of two different monosaccharides. C)It contains both an acetal and a hemiacetal. D)It contains a 1→5-α-glycosidic linkage. <div style=padding-top: 35px>

A)It is a disaccharide.
B)It is composed of two different monosaccharides.
C)It contains both an acetal and a hemiacetal.
D)It contains a 1→5-α-glycosidic linkage.
Question
Which of the following is not a term that would properly describe glucose as it is shown below? <strong>Which of the following is not a term that would properly describe glucose as it is shown below?  </strong> A)Monosaccharide B)Aldohexose C)Reducing sugar D)β-D-glucose <div style=padding-top: 35px>

A)Monosaccharide
B)Aldohexose
C)Reducing sugar
D)β-D-glucose
Question
Which structure is a three-carbon alditol?

A) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The monosaccharide shown below is an α anomer. The monosaccharide shown below is an α anomer.  <div style=padding-top: 35px>
Question
Which naturally-occurring monosaccharide forms the Haworth structure shown? <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Which is not a reducing sugar?

A)Glucose
B)Fructose
C)Sucrose
D)Galactose
E)An aldopentose
Question
What is the difference between the disaccharides lactose and maltose?

A)Lactose contains two glucose units,while maltose contains two galactose units.
B)The two monosaccharides in lactose are joined by a 1→4-β-glycoside bond,while the two monosaccharides in maltose are joined by a 1→4-α-glycoside bond.
C)Lactose contains both an acetal and a hemiacetal,while maltose contains two acetals.
D)Lactose can be hydrolyzed in the body,but maltose cannot.
Question
What type of polysaccharide is depicted in the "cartoon" shown below? <strong>What type of polysaccharide is depicted in the cartoon shown below?  </strong> A)Cellulose B)Amylose C)Amylopectin D)Chitin <div style=padding-top: 35px>

A)Cellulose
B)Amylose
C)Amylopectin
D)Chitin
Question
The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?

A) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
All disaccharides contain at least one acetal that joins the rings together.
Question
An α glycoside has the glycosidic linkage oriented down,below the plane of the ring that contains the acetal joining the monosaccharides.
Question
Modern glucose meters are electronic devices that measure the amount of oxidizing agent that reacts with the glucose in a known amount of blood.
Question
All aldoses and ketoses are reducing sugars.
Question
The carbonyl group of an aldose is reduced to a secondary alcohol using hydrogen (H2)in the presence of palladium (Pd)metal.
Question
The two compounds N-acetyl-D-glucosamine and N-acetyl-D-galactosamine are a set of constitutional isomers.
Question
When the monosaccharide below is oxidized by Benedict's reagent,the indicated product results. When the monosaccharide below is oxidized by Benedict's reagent,the indicated product results.  <div style=padding-top: 35px>
Question
The structure shown has four (4)chirality centers and is a D monosaccharide. The structure shown has four (4)chirality centers and is a D monosaccharide.  <div style=padding-top: 35px>
Question
In aldohexoses,it is the -OH group on C5 that reacts with the aldehyde carbonyl to form two cyclic hemiacetals called anomers.
Question
Hydrolysis of the disaccharide below yields the indicated products. Hydrolysis of the disaccharide below yields the indicated products.  <div style=padding-top: 35px>
Question
α-D-galactose and β-D-galactose are enantiomers.
Question
Cellulose is a highly-branched polymer composed of repeating glucose units joined in a 1→4-β-glycosidic linkage.
Question
In addition to the three monosaccharides that occur in all blood types,type A blood contains the monosaccharide N-acetyl-D-galactosamine,and type B blood contains an additional D-galactose unit.
Question
Glucose and other naturally occurring sugars are D sugars.
Question
The disaccharide shown below has an α-glycosidic linkage. The disaccharide shown below has an α-glycosidic linkage.  <div style=padding-top: 35px>
Question
Carbohydrates that are oxidized with Benedict's reagent are called reducing sugars,because they reduce the Cu2+ in Benedict's reagent to Cu+ during the reaction.
Question
An alditol contains an -OH group on every carbon atom.
Question
Individuals with type AB blood are called universal recipients because their blood contains no antibodies to blood types A,B,or O. Individuals with type AB blood can receive blood of any type.
Question
Maltose is a reducing sugar.
Question
Test strips that contain the enzyme lactase are used to measure glucose concentration in urine.
Unlock Deck
Sign up to unlock the cards in this deck!
Unlock Deck
Unlock Deck
1/100
auto play flashcards
Play
simple tutorial
Full screen (f)
exit full mode
Deck 20: Carbohydrates
1
What product forms when the compound below is treated with H2 in the presence of a Pd catalyst? <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)

A) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
B) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
C) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
D) <strong>What product forms when the compound below is treated with H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
2
When converting a Fischer projection to a Haworth projection,where are all of the substituents on the right side of the carbon skeleton drawn in the Haworth projection?

A)Down
B)Up
C)Down in an α anomer and up in a β anomer
D)Down in an β anomer and up in a α anomer
Down
3
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)Aldohexose B)Aldopentose C)Ketotetrose D)Ketopentose

A)Aldohexose
B)Aldopentose
C)Ketotetrose
D)Ketopentose
Aldopentose
4
What are monosaccharides with a carbonyl group at C1 called?

A)Anomers
B)Aldoses
C)Ketoses
D)Alditols
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
5
Which carbohydrates cannot be converted to simpler compounds by hydrolysis?

A)Disaccharides
B)Monosaccharides
C)Polysaccharides
D)Starches
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
6
Which monosaccharide is an aldotriose?

A) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)
B) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)
C) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)
D) <strong>Which monosaccharide is an aldotriose?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
7
In the monosaccharide given,which of the labeled carbons are chiral centers? <strong>In the monosaccharide given,which of the labeled carbons are chiral centers?  </strong> A)C<sub>1 </sub>is the only chiral center. B)C<sub>1</sub> and C<sub>2</sub> are both chiral centers. C)C<sub>2</sub> and C<sub>3</sub> are both chiral centers D)C<sub>3</sub> is the only chiral center

A)C1 is the only chiral center.
B)C1 and C2 are both chiral centers.
C)C2 and C3 are both chiral centers
D)C3 is the only chiral center
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
8
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)An aldohexose B)A ketohexose C)An aldopentose D)A ketopentose

A)An aldohexose
B)A ketohexose
C)An aldopentose
D)A ketopentose
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
9
How many chirality centers are present in the compound shown below? <strong>How many chirality centers are present in the compound shown below?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
10
How many chirality centers are present in the compound shown below? <strong>How many chirality centers are present in the compound shown below?  </strong> A)2 B)4 C)5 D)6

A)2
B)4
C)5
D)6
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
11
Which Haworth projection represents the banomer of the monosaccharide shown below? <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)

A) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
B) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
C) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
D) <strong>Which Haworth projection represents the banomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
12
Which of the following is a ketohexose?

A) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)
B) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)
C) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)
D) <strong>Which of the following is a ketohexose?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
13
What is the classification of the monosaccharide shown? <strong>What is the classification of the monosaccharide shown?  </strong> A)L B)D C)A sugar this large is not classified as L or D.

A)L
B)D
C)A sugar this large is not classified as L or D.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
14
Which compound is the most soluble in water?

A)CH2OHCHOHCHOHCHOHCHOHCHO
B)CH3CH2CH=CHCH2CH=CHCH2CH2CH2CH2CH2CH2CH2COOH
C)CH3CH2CH2CH2CH2CH2CH2CH2CH3
D)CH3CH2CH2CH2CH2CH2CH2CH2OH
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
15
Which labeled carbon atom in the structure below is the anomeric carbon? <strong>Which labeled carbon atom in the structure below is the anomeric carbon?  </strong> A)A B)B C)C D)D

A)A
B)B
C)C
D)D
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
16
Which Haworth projection represents the α anomer of the monosaccharide shown below? <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)

A) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
B) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
C) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
D) <strong>Which Haworth projection represents the α anomer of the monosaccharide shown below?  </strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
17
The structures of galactose (left)and glucose (right)are shown below. How are the two monosaccharides related? <strong>The structures of galactose (left)and glucose (right)are shown below. How are the two monosaccharides related?  </strong> A)Structural isomers B)Stereoisomers C)Enantiomers D)Anomers

A)Structural isomers
B)Stereoisomers
C)Enantiomers
D)Anomers
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
18
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)A tetraketose B)A ketotriose C)A ketotetrose D)An aldotriose

A)A tetraketose
B)A ketotriose
C)A ketotetrose
D)An aldotriose
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
19
The formation of what color in the Benedict's test indicates a reducing sugar is present in solution?

A)Blue
B)Brick red
C)Bright yellow
D)Silver
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
20
What is the classification of the compound shown below? <strong>What is the classification of the compound shown below?  </strong> A)L B)D C)A sugar this small is not classified as L or D.

A)L
B)D
C)A sugar this small is not classified as L or D.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
21
Which is the only polysaccharide to have β-glycosidic bonds?

A)Glycogen
B)Amylose
C)Cellulose
D)Amylopectin
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
22
What is the most common type of starch molecules?

A)Cellulose
B)Amylose
C)Amylopectin
D)Glycogen
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
23
Which choice properly describes the glycoside bond in the disaccharide below? <strong>Which choice properly describes the glycoside bond in the disaccharide below?  </strong> A)1→6-α B)1→6-β C)1→4α D)1→4β

A)1→6-α
B)1→6-β
C)1→4α
D)1→4β
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
24
What product forms when the compound below is treated with Benedict's reagent? <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)

A) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)
B) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)
C) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)
D) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
25
How many acetals and hemiacetals are present in the disaccharide below? <strong>How many acetals and hemiacetals are present in the disaccharide below?  </strong> A)Two acetals are present. B)Two hemiacetals are present. C)One hemiacetal and one acetal is present D)No hemiacetals or acetals are present.

A)Two acetals are present.
B)Two hemiacetals are present.
C)One hemiacetal and one acetal is present
D)No hemiacetals or acetals are present.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
26
What is responsible for the different blood types in humans?

A)Three or four proteins attached to a membrane monosaccharide on the surface of red blood cells
B)Three or four monosaccharides attached to a membrane protein on the surface of red blood cells
C)Three or four amino acids attached to a membrane monosaccharide on the surface of red blood cells
D)Three or four lipids attached to a membrane polysaccharide on the surface of red blood cells
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
27
Which is not a naturally-occurring polysaccharide?

A)Starch
B)Cellulose
C)Maltose
D)Glycogen
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
28
Which is not a glycosaminoglycan?

A)Hyaluronate
B)Chitin
C)Heparin
D)Chondroitin
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
29
Which carbohydrate derivative forms a gel-like matrix in joints and the vitreous humor of the eye?

A)Heparin
B)Chondroitin
C)Hyaluronate
D)Chitin
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
30
What is the structure of amylopectin?

A)Unbranched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
B)Branched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
C)Unbranched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
D)Branched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
31
Chitin is identical in structure to cellulose,except that

A)The linkages are a-glycoside linkages.
B)Each OH group at C4 is replaced by NHCOCH3.
C)Each OH group at C2 is replaced by NH3.
D)Each OH group at C2 is replaced by NHCOCH3.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
32
What product forms when the compound below is treated with Benedict's reagent? <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs.

A) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs.
B) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs.
C) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs.
D) <strong>What product forms when the compound below is treated with Benedict's reagent?  </strong> A)   B)   C)   D)   E)No reaction occurs.
E)No reaction occurs.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
33
Salicin is a naturally occurring,carbohydrate-containing pain reliever. Which statement concerning the functional groups present in salicin is incorrect? <strong>Salicin is a naturally occurring,carbohydrate-containing pain reliever. Which statement concerning the functional groups present in salicin is incorrect?  </strong> A)Salicin contains an acetal. B)Salicin contains an alcohol. C)Salicin contains a hemiacetal. D)Salicin contains a phenol.

A)Salicin contains an acetal.
B)Salicin contains an alcohol.
C)Salicin contains a hemiacetal.
D)Salicin contains a phenol.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
34
What is the structure of cellulose?

A)Unbranched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
B)Branched skeleton of glucose molecules joined by 1→4-α-glycoside linkages
C)Unbranched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
D)Branched skeleton of glucose molecules joined by 1→4-β-glycoside linkages
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
35
Why are humans not able to digest cellulose?

A)Humans cannot digest glucose.
B)Humans do not possess the enzyme necessary to hydrolyze the 1→4-β-glycoside linkages found in cellulose.
C)Humans do not possess the enzyme necessary to unwind the helical shape of the cellulose molecule.
D)Humans do not possess the enzyme necessary to hydrolyze the 1→4-α-glycoside linkages found in cellulose.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
36
Disaccharides and polysaccharides contain monosaccharide units joined together by which of the following?

A)Hydrogen bonding
B)Glycosidic linkages
C)Hemiacetal bonds
D)Dipole-dipole forces
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
37
What is the polysaccharide form in which glucose is stored in animals?

A)Cellulose
B)Amylose
C)Amylopectin
D)Glycogen
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
38
How many acetals are present in the disaccharide shown below? <strong>How many acetals are present in the disaccharide shown below?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
39
Lactose is present in milk. What type of sugar is lactose?

A)A disaccharide
B)A monosaccharide
C)A polysaccharide
D)A starch
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
40
What monosaccharide is found in cellulose,starch,and glycogen?

A)Glucose
B)Galactose
C)Sucrose
D)Fructose
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
41
Dihydroxyacetone,shown below,is the simplest ketose. Does the structure shown represent D-dihydroxyacetone or L-dihydroxyacetone? <strong>Dihydroxyacetone,shown below,is the simplest ketose. Does the structure shown represent D-dihydroxyacetone or L-dihydroxyacetone?  </strong> A)D-dihydroxyacetone B)L-dihydroxyacetone C)Neither D nor L; dihydroxyacetone is not chiral D)It is impossible to tell from the Fischer projection alone.

A)D-dihydroxyacetone
B)L-dihydroxyacetone
C)Neither D nor L; dihydroxyacetone is not chiral
D)It is impossible to tell from the Fischer projection alone.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
42
Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product? <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)

A) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)
B) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)
C) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)
D) <strong>Gentobiose,a rare disaccharide found in saffron,produces two identical monosaccharides when it undergoes hydrolysis. What is the identity of the hydrolysis product?  </strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
43
The monosaccharide shown below is an α anomer. The monosaccharide shown below is an α anomer.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
44
At equilibrium,a solution of glucose in water is an equal mixture of the α anomer,the β anomer,and the acyclic aldehyde.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
45
When a monosaccharide forms a cyclic hemiacetal,the carbon atom that is part of the hemiacetal is a new chirality center,called the anomeric carbon.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
46
The β anomer of a cyclic monosaccharide has the -OH group drawn down,below the ring.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
47
The Fischer projections of two monosaccharides are shown below. Which term best describes the relationship between the two? <strong>The Fischer projections of two monosaccharides are shown below. Which term best describes the relationship between the two?  </strong> A)Enantiomers B)Anomers C)Constitutional isomers D)Diastereomers

A)Enantiomers
B)Anomers
C)Constitutional isomers
D)Diastereomers
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
48
Which statement concerning carbohydrates is incorrect?

A)Carbohydrates serve important energy and structural roles for both plants and animals.
B)Monosaccharides are the simplest carbohydrates and are known as simple sugars.
C)Humans store excess glucose for short term energy requirements in the polysaccharide cellulose.
D)Carbohydrates that can be oxidized by Benedict's reagent are called reducing sugars.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
49
A hemiacetal is a compound that contains a hydroxyl group (-OH)and an alkoxy group (-OR)on adjacent carbon atoms.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
50
The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?

A) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)
B) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)
C) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)
D) <strong>The simplest aldose is commonly called glyceraldehyde,although its IUPAC name is 2,3-dihydroxypropanal. What is the structure of this compound?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
51
Certain monosaccharides-notably aldopentoses and ketohexoses-form five-membered rings,not six-membered rings,in solution.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
52
Melibiose is a carbohydrate found in some plant juices. Which statement concerning melibiose is incorrect? <strong>Melibiose is a carbohydrate found in some plant juices. Which statement concerning melibiose is incorrect?  </strong> A)It is a disaccharide. B)It is composed of two different monosaccharides. C)It contains both an acetal and a hemiacetal. D)It contains a 1→5-α-glycosidic linkage.

A)It is a disaccharide.
B)It is composed of two different monosaccharides.
C)It contains both an acetal and a hemiacetal.
D)It contains a 1→5-α-glycosidic linkage.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
53
Which of the following is not a term that would properly describe glucose as it is shown below? <strong>Which of the following is not a term that would properly describe glucose as it is shown below?  </strong> A)Monosaccharide B)Aldohexose C)Reducing sugar D)β-D-glucose

A)Monosaccharide
B)Aldohexose
C)Reducing sugar
D)β-D-glucose
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
54
Which structure is a three-carbon alditol?

A) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)
B) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)
C) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)
D) <strong>Which structure is a three-carbon alditol?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
55
The monosaccharide shown below is an α anomer. The monosaccharide shown below is an α anomer.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
56
Which naturally-occurring monosaccharide forms the Haworth structure shown? <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)

A) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)
B) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)
C) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)
D) <strong>Which naturally-occurring monosaccharide forms the Haworth structure shown?  </strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
57
Which is not a reducing sugar?

A)Glucose
B)Fructose
C)Sucrose
D)Galactose
E)An aldopentose
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
58
What is the difference between the disaccharides lactose and maltose?

A)Lactose contains two glucose units,while maltose contains two galactose units.
B)The two monosaccharides in lactose are joined by a 1→4-β-glycoside bond,while the two monosaccharides in maltose are joined by a 1→4-α-glycoside bond.
C)Lactose contains both an acetal and a hemiacetal,while maltose contains two acetals.
D)Lactose can be hydrolyzed in the body,but maltose cannot.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
59
What type of polysaccharide is depicted in the "cartoon" shown below? <strong>What type of polysaccharide is depicted in the cartoon shown below?  </strong> A)Cellulose B)Amylose C)Amylopectin D)Chitin

A)Cellulose
B)Amylose
C)Amylopectin
D)Chitin
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
60
The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?

A) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)
B) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)
C) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)
D) <strong>The simplest aldose is commonly called dihydroxyacetone,although its IUPAC name is 1,3-dihydroxy-2-propanone. What is the structure of this compound?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
61
All disaccharides contain at least one acetal that joins the rings together.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
62
An α glycoside has the glycosidic linkage oriented down,below the plane of the ring that contains the acetal joining the monosaccharides.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
63
Modern glucose meters are electronic devices that measure the amount of oxidizing agent that reacts with the glucose in a known amount of blood.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
64
All aldoses and ketoses are reducing sugars.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
65
The carbonyl group of an aldose is reduced to a secondary alcohol using hydrogen (H2)in the presence of palladium (Pd)metal.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
66
The two compounds N-acetyl-D-glucosamine and N-acetyl-D-galactosamine are a set of constitutional isomers.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
67
When the monosaccharide below is oxidized by Benedict's reagent,the indicated product results. When the monosaccharide below is oxidized by Benedict's reagent,the indicated product results.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
68
The structure shown has four (4)chirality centers and is a D monosaccharide. The structure shown has four (4)chirality centers and is a D monosaccharide.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
69
In aldohexoses,it is the -OH group on C5 that reacts with the aldehyde carbonyl to form two cyclic hemiacetals called anomers.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
70
Hydrolysis of the disaccharide below yields the indicated products. Hydrolysis of the disaccharide below yields the indicated products.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
71
α-D-galactose and β-D-galactose are enantiomers.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
72
Cellulose is a highly-branched polymer composed of repeating glucose units joined in a 1→4-β-glycosidic linkage.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
73
In addition to the three monosaccharides that occur in all blood types,type A blood contains the monosaccharide N-acetyl-D-galactosamine,and type B blood contains an additional D-galactose unit.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
74
Glucose and other naturally occurring sugars are D sugars.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
75
The disaccharide shown below has an α-glycosidic linkage. The disaccharide shown below has an α-glycosidic linkage.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
76
Carbohydrates that are oxidized with Benedict's reagent are called reducing sugars,because they reduce the Cu2+ in Benedict's reagent to Cu+ during the reaction.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
77
An alditol contains an -OH group on every carbon atom.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
78
Individuals with type AB blood are called universal recipients because their blood contains no antibodies to blood types A,B,or O. Individuals with type AB blood can receive blood of any type.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
79
Maltose is a reducing sugar.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
80
Test strips that contain the enzyme lactase are used to measure glucose concentration in urine.
Unlock Deck
Unlock for access to all 100 flashcards in this deck.
Unlock Deck
k this deck
locked card icon
Unlock Deck
Unlock for access to all 100 flashcards in this deck.