Biochemistry : Identification by Structure
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Example Questions
Example Question #31 : Identification By Structure
Identify the carbohydrate class of the given molecule.
Aldopentose
Aldoquintos
Aldohexose
Ketohexose
Ketopentose
Aldopentose
The structure is an aldopentose. Aldo- refers to the aldehyde at the first carbon and pentose refers to a carbohydrate with five carbons.
Example Question #31 : Identification By Structure
Identify the carbohydrate class of the given molecule.
Ketoquintos
Ketopentose
Ketohexose
Aldohexose
Aldopentose
Ketopentose
The structure is a ketopentose. Keto- refers to the ketone at the second carbon and pentose refers to a carbohydrate with five carbons.
Example Question #32 : Identification By Structure
Identify the given structure.
D-glucose
L-glucose
D-galactose
L-galactose
D-fructose
D-glucose
This ring structure is of D-glucose. The hydroxyl group on the first carbon (the carbon to the bottom right of the oxygenin the ring) can face either down (the alpha conformation) or up (the beta conformation). Note that the beta conformer is more thermodynamically stable since all the hydroxyl groups on the ring would be in the equitorial position, thus minimizing steric hinderance and intramolecular electrostatic repulsion.
Example Question #33 : Identification By Structure
Identify the given structure.
D-fructose
D-glucose
D-galactose
D-mannose
D-ribose
D-fructose
This is the ring/cyclic structure of D-fructose.
Example Question #81 : Identifying Biochemical Molecules
Which of the following is the correct structure of a disaccharide?
Lactose = galactose + galactose
Sucrose = glucose + glucose
Maltose = glucose + glucose
Lactose = galactose + fructose
Maltose = sucrose + fructose
Maltose = glucose + glucose
The correct structures of the disaccharides are:
Maltose = glucose + glucose
Sucrose = glucose + fructose
Lactose = glucose + galactose
Example Question #91 : Identifying Biochemical Molecules
Which amino acid does this structure represent?
Arginine
Glutamine
Aspartate
Asparagine
Glutamate
Glutamate
The amino acid's R group is composed of an ethyl group, followed by a carboxylate group, and therefore represents glutamate.
Example Question #33 : Identification By Structure
Which amino acid does this structure represent?
S
A
M
Y
T
M
The amino acid's chiral carbon is connected to two methyl groups followed, by a sulfur, and finally another methyl group. Therefore, the amino acid is methionine (M).
Example Question #1 : Identifying Specific Protein Structures
The amino acid phenylalanine is pictured. If a hydroxyl group was added to the carbon in the red box, which amino acid would the new molecule most closely resemble?
Glysine
Lysine
Tyrosine
Alanine
Arginine
Tyrosine
The structure would most closely resembe tyrosine (pictured).
Example Question #36 : Identification By Structure
If the phenyl group in the pictured molecule were removed, what amino acid would the new structure most closely resemble?
Phenylalanine
Alanine
Valine
Tyrosine
Glycine
Alanine
Alanine is the amino acid that would be formed by removing the phenyl group from phenylalanine (the pictured molecule).
Example Question #37 : Identification By Structure
If the amide group of glutamine (pictured here) was removed and a hydroxyl group was added to the carbon bound to the alpha carbon of the resulting structure, what amino acid would be formed?
Cysteine
Threonine
Methionine
Tyrosine
Valine
Threonine
Threonine (pictured here) would be formed.
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