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Example Questions
Example Question #251 : Biochemistry
Which of the following ring structures represents the anomeric alpha ring structure of D-mannose?
When converting a linear sugar to its ring form, a bond is formed between the oxygen attached to carbon 5 and the carbon at position 1. All hydroxyl groups that are not attached to the carbon in position 1 and are oriented to the right end up trans to the attached to carbon 5, while those that are in the left position end up cis to the attached to carbon 5.
If the hydroxyl group attached to carbon 1 ends up trans to the attached to carbon 5, the ring structure is considered alpha. If the hydroxyl group attached to carbon 1 is cis to the attached to carbon 5, the ring structure is considered beta.
The alpha ring structure of D-mannose bonds the carbon 1 hydroxyl group trans to the carbon 5 group. The hyroxyl groups on carbons 2, 3, and 4 will be cis, cis, and trans with respect to the .
Example Question #252 : Biochemistry
Identify the aldose pictured, including its alpha or beta designation.
-D-mannose
-D-ribose
-D-glucose
-D-glucose
-D-mannose
-D-mannose
The structure pictured is mannose because the hydroxyl groups at carbons 2, 3, and 4 are situated cis, cis, and trans (respectively) to the attached to carbon 5.
The mannose pictured is in alpha form because the hydroxyl group at carbon 1 is trans to the attached to carbon 5.
Example Question #253 : Biochemistry
The Fischer projection pictured is a form of glucose. The carbon labeled "x" is the chiral carbon farthest away from carbon 1 and the hydroxyl group connected to carbon "x" is on the right. This fact designates that the glucose as what configuration?
Alpha
L
D
Beta
Pyranose
D
The chiral carbon farthest away from carbon 1 is designated as "D" if its hydroxyl group is on the right side in the Fischer projection. In other words, this is D-glucose because the hyroxyl group on carbon "x" is oriented to the right.
Example Question #254 : Biochemistry
What is the name of the aldose pictured in this Fischer projection?
L-lyxose
L-xylose
L-fructose
D-ribose
D-arabinose
D-ribose
The structure is D-ribose because it is a five-carbon aldose with the hydroxyl groups on carbons 2, 3, and 4 all on the right in the Fischer projection.
Example Question #42 : Identifying Monomers And Dimers
Which of the following is not a monosaccharide?
Galactose
Fructose
All of these are monosaccharides
Lactose
Glucose
Lactose
While glucose, galactose, and fructose are all monosaccharides, lactose is a disaccharide comprised of two monosaccharides, glucose and galactose, joined by a -1,4-glycosidic bond.
Example Question #254 : Biochemistry
L-Glucose is found as 2 different hexose stereoisomers in solution: and glucose.
Suppose both and L-glucose were polymerized into long glycosidic linkages. Which of the two polymers could be catabolized (broken down into component parts) by a human?
-L-glucose
Both stereoisomers
Neither stereoisomer
-L-glucose
Neither stereoisomer
In nature, L-sugars are indigestible by humans. In the case of L-glucose, even though our bodies can break down polymers of -D-glucose, it cannot digest L-glucose.
Example Question #43 : Identifying Monomers And Dimers
Which of the following compounds is not a monosaccharide?
Galactose
Lactose
Fructose
Ribose
Glucose
Lactose
Out of all the sugars listed, lactose is the only one that is not a monosaccharide. Lactose is composed of a glucose and galactose bound together in a glycosidic linkage.
Example Question #43 : Identifying Monomers And Dimers
Which sugar is another name for "blood sugar?"
Fructose
Glucose
Sucrose
Lactose
Glucose
Glucose is also called "blood sugar" because it is the main sugar found in our blood. Sucrose is what we know as "table sugar" because it is commonly found in our kitchens and used in baking etc. Fructose is also known as "fruit sugar" because it occurs in naturally-occurring fruits, giving them their sweetness. Lactose is sometimes called "milk sugar" because it is found in milk.
Example Question #1 : Identifying Disaccharides
Which of the following is not a disaccharide?
All of these are disaccharides
Cellobiose
Sucrose
Maltose
Lactose
All of these are disaccharides
Review the specific types of monosaccharides and glycosidic bonds that are involved in these disaccharides. Remember that disaccharides are formed upon dehydration synthesis of two monosaccharides.
Maltose is composed of two glucose monomers with an 1-4 linkage.
Cellobiose is composed of two glucose monomers with a 1-4 linkage.
Sucrose is composed of one glucose monomer and one fructose monomer with an 1-2 linkage.
Lactose is composed of one galactose monomer and one glucose monomer with a 1-4 linkage.
Example Question #1 : Identifying Disaccharides
Maltose is a disaccharide composed of which two monosaccharides?
Glucose + fructose
Glucose + glucose
Glucose + galactose
Fructose + fructose
Galactose + galactose
Glucose + glucose
Maltose, which is made up of two glucose monomers joined by an alpha-1,4 linkage, is the correct answer. On the other hand, lactose is made up of one glucose monomer and one galactose monomer, and sucrose is made up of one glucose monomer and one fructose monomer.
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