Two sugars which differ from one another only in configuration around a single carbon atom are termed (A) Epimers (B) Anomers (C) Optical isomers (D) Stereoisomers

Two sugars which differ from one another
only in configuration around a single
carbon atom are termed
(A) Epimers (B) Anomers
(C) Optical isomers (D) Stereoisomers
by

1 Answer

Answer :

(A) Epimers
by

Related questions

Two sugars which differ from one another only in configuration around a single carbon atom are termed (A) Epimers (B) Anomers (C) Optical isomers (D) Stereoisomers

Description : Two sugars which differ from one another only in configuration around a single carbon atom are termed (A) Epimers (B) Anomers (C) Optical isomers (D) Stereoisomers

Last Answer : A

Compounds having the same structural formula but differing in spatial configuration are known as (A) Stereoisomers (B) Anomers (C) Optical isomers (D) Epimers

Description : Compounds having the same structural formula but differing in spatial configuration are known as (A) Stereoisomers (B) Anomers (C) Optical isomers (D) Epimers

Last Answer : (A) Stereoisomers

Isomers differing as a result of variations in configuration of the —OH and —H on carbon atoms 2, 3 and 4 of glucose are known as (A) Epimers (B) Anomers (C) Optical isomers (D) Steroisomers

Description : Isomers differing as a result of variations in configuration of the —OH and —H on carbon atoms 2, 3 and 4 of glucose are known as (A) Epimers (B) Anomers (C) Optical isomers (D) Steroisomers

Last Answer : (A) Epimers

In glucose the orientation of the —H and —OH groups around the carbon atom 5 adjacent to the terminal primary alcohol carbon determines (A) D or L series (B) Dextro or levorotatory (C)  and  anomers (D) Epimers

Description : In glucose the orientation of the —H and —OH groups around the carbon atom 5 adjacent to the terminal primary alcohol carbon determines (A) D or L series (B) Dextro or levorotatory (C)  and  anomers (D) Epimers

Last Answer : (A) D or L series

Compounds having the same structural formula but differing in spatial configuration are known as (A) Stereoisomers (B) Anomers (C) Optical isomers (D) Epimers

Description : Compounds having the same structural formula but differing in spatial configuration are known as (A) Stereoisomers (B) Anomers (C) Optical isomers (D) Epimers

Last Answer : A

Isomers differing as a result of variations in configuration of the —OH and —H on carbon atoms 2, 3 and 4 of glucose are known as (A) Epimers (B) Anomers (C) Optical isomers (D) Steroisomers

Description : Isomers differing as a result of variations in configuration of the —OH and —H on carbon atoms 2, 3 and 4 of glucose are known as (A) Epimers (B) Anomers (C) Optical isomers (D) Steroisomers

Last Answer : A

In glucose the orientation of the —H and —OH groups around the carbon atom 5 adjacent to the terminal primary alcohol carbon determines (A) D or L series (B) Dextro or levorotatory (C) α and β anomers (D) Epimers

Description : In glucose the orientation of the —H and —OH groups around the carbon atom 5 adjacent to the terminal primary alcohol carbon determines (A) D or L series (B) Dextro or levorotatory (C) α and β anomers (D) Epimers

Last Answer : A

α-D-glucose and β -D-glucose are (A) Stereoisomers (B) Epimers (C) Anomers (D) Keto-aldo pairs

Description : α-D-glucose and β -D-glucose are (A) Stereoisomers (B) Epimers (C) Anomers (D) Keto-aldo pairs

Last Answer : C

The number of isomers of glucose is (A) 2 (B) 4 (C) 8 (D) 16

Description : The number of isomers of glucose is (A) 2 (B) 4 (C) 8 (D) 16

Last Answer : (D) 16

α−D-Glucose and β−D-glucose are related by (A) Epimers (B) Anomers (C) Multirotation (D) Ketoenol pair

Description : α−D-Glucose and β−D-glucose are related by (A) Epimers (B) Anomers (C) Multirotation (D) Ketoenol pair

Last Answer : B

The true statement about solutions of amino acids at physiological pH is (A) All amino acids contain both positive and negative charges (B) All amino acids contain positively charged side chains (C) Some amino acids contain only positive Charge (D) All amino acids contain negatively charged side chains

Description : The true statement about solutions of amino acids at physiological pH is (A) All amino acids contain both positive and negative charges (B) All amino acids contain positively charged side chains ... amino acids contain only positive Charge (D) All amino acids contain negatively charged side chains

Last Answer : (A) All amino acids contain both positive and negative charges

Proteins contain (A) Only L-  - amino acids (B) Only D-amino acids (C) DL-Amino acids (D) Both (A) and (B)

Description : Proteins contain (A) Only L-  - amino acids (B) Only D-amino acids (C) DL-Amino acids (D) Both (A) and (B)

Last Answer : (A) Only L-  - amino acids

All proteins contain the (A) Same 20 amino acids (B) Different amino acids (C) 300 Amino acids occurring in nature (D) Only a few amino acids

Description : All proteins contain the (A) Same 20 amino acids (B) Different amino acids (C) 300 Amino acids occurring in nature (D) Only a few amino acids

Last Answer : (A) Same 20 amino acids

Non essential amino acids (A) Are not components of tissue proteins (B) May be synthesized in the body from essential amino acids (C) Have no role in the metabolism (D) May be synthesized in the body in diseased states

Description : Non essential amino acids (A) Are not components of tissue proteins (B) May be synthesized in the body from essential amino acids (C) Have no role in the metabolism (D) May be synthesized in the body in diseased states

Last Answer : (B) May be synthesized in the body from essential amino acids

An example of -amino acid not present in proteins but essential in mammalian metabolism is (A) 3-Amino 3-hydroxypropanoic acid (B) 2-Amino 3-hydroxybutanoic acid (C) 2-Amino 4-mercaptobutanoic acid (D) 2-Amino 3-mercaptopropanoic acid

Description : An example of -amino acid not present in proteins but essential in mammalian metabolism is (A) 3-Amino 3-hydroxypropanoic acid (B) 2-Amino 3-hydroxybutanoic acid (C) 2-Amino 4-mercaptobutanoic acid (D) 2-Amino 3-mercaptopropanoic acid

Last Answer : (C) 2-Amino 4-mercaptobutanoic acid

Amino acid with side chain containing basic groups is (A) 2-Amino 5-guanidovaleric acid (B) 2-Pyrrolidine carboxylic acid (C) 2-Amino 3-mercaptopropanoic acid (D) 2-Amino propanoic acid

Description : Amino acid with side chain containing basic groups is (A) 2-Amino 5-guanidovaleric acid (B) 2-Pyrrolidine carboxylic acid (C) 2-Amino 3-mercaptopropanoic acid (D) 2-Amino propanoic acid

Last Answer : (A) 2-Amino 5-guanidovaleric acid

The functions of plasma albumin are (A) Osmosis (B) Transport (C) Immunity (D) both (A )and (B)

Description : The functions of plasma albumin are (A) Osmosis (B) Transport (C) Immunity (D) both (A )and (B)

Last Answer : (A) Osmosis

An aromatic amino acid is (A) Lysine (B) Tyrosine (C) Taurine (D) Arginine

Description : An aromatic amino acid is (A) Lysine (B) Tyrosine (C) Taurine (D) Arginine

Last Answer : (B) Tyrosine

All the following are sulphur containing amino acids found in proteins except (A) Cysteine (B) Cystine (C) Methionine (D) Threonine

Description : All the following are sulphur containing amino acids found in proteins except (A) Cysteine (B) Cystine (C) Methionine (D) Threonine

Last Answer : (D) Threonine

An example of sulphur containing amino acid is (A) 2-Amino-3-mercaptopropanoic acid (B) 2-Amino-3-methylbutanoic acid (C) 2-Amino-3-hydroxypropanoic acid (D) Amino acetic acid

Description : An example of sulphur containing amino acid is (A) 2-Amino-3-mercaptopropanoic acid (B) 2-Amino-3-methylbutanoic acid (C) 2-Amino-3-hydroxypropanoic acid (D) Amino acetic acid

Last Answer : (A) 2-Amino-3-mercaptopropanoic acid

Sulphur containing amino acid is (A) Methionine (B) Leucine (C) Valine (D) Asparagine

Description : Sulphur containing amino acid is (A) Methionine (B) Leucine (C) Valine (D) Asparagine

Last Answer : (A) Methionine

Since the pK values for aspartic acid are 2.0, 3.9 and 10.0, it follows that the isoelectric (pH) is (A) 3.0 (B) 3.9 (C) 5.9 (D) 6.0

Description : Since the pK values for aspartic acid are 2.0, 3.9 and 10.0, it follows that the isoelectric (pH) is (A) 3.0 (B) 3.9 (C) 5.9 (D) 6.0

Last Answer : (A) 3.0

pH (isoelectric pH) of alanine is (A) 6.02 (B) 6.6 (C) 6.8 (D) 7.2

Description : pH (isoelectric pH) of alanine is (A) 6.02 (B) 6.6 (C) 6.8 (D) 7.2

Last Answer : (A) 6.02

At neutral pH, a mixture of amino acids in solution would be predominantly: (A) Dipolar ions (B) Nonpolar molecules (C) Positive and monovalent (D) Hydrophobic

Description : At neutral pH, a mixture of amino acids in solution would be predominantly: (A) Dipolar ions (B) Nonpolar molecules (C) Positive and monovalent (D) Hydrophobic

Last Answer : (A) Dipolar ions

The optically inactive amino acid is (A) Glycine (B) Serine (C) Threonine (D) Valine

Description : The optically inactive amino acid is (A) Glycine (B) Serine (C) Threonine (D) Valine

Last Answer : (A) Glycine

The sugar found in DNA is (A) Xylose (B) Ribose (C) Deoxyribose (D) Ribulose

Description : The sugar found in DNA is (A) Xylose (B) Ribose (C) Deoxyribose (D) Ribulose

Last Answer : (C) Deoxyribose

The major sugar of insect hemolymph is (A) Glycogen (B) Pectin (C) Trehalose (D) Sucrose

Description : The major sugar of insect hemolymph is (A) Glycogen (B) Pectin (C) Trehalose (D) Sucrose

Last Answer : (C) Trehalose

A sugar alcohol is (A) Mannitol (B) Trehalose (C) Xylulose (D) Arabinose

Description : A sugar alcohol is (A) Mannitol (B) Trehalose (C) Xylulose (D) Arabinose

Last Answer : (A) Mannitol

Erythromycin contains (A) Dimethyl amino sugar (B) Trimethyl amino sugar (C) Sterol and sugar (D) Glycerol and sugar

Description : Erythromycin contains (A) Dimethyl amino sugar (B) Trimethyl amino sugar (C) Sterol and sugar (D) Glycerol and sugar

Last Answer : (A) Dimethyl amino sugar

The carbohydrate of the blood group substances is (A) Sucrose (B) Fucose (C) Arabinose (D) Maltose

Description : The carbohydrate of the blood group substances is (A) Sucrose (B) Fucose (C) Arabinose (D) Maltose

Last Answer : (B) Fucose

The most important epimer of glucose is (A) Galactose (B) Fructose (C) Arabinose (D) Xylose

Description : The most important epimer of glucose is (A) Galactose (B) Fructose (C) Arabinose (D) Xylose

Last Answer : (A) Galactose

Polysaccharides are (A) Polymers (B) Acids (C) Proteins (D) Oils

Description : Polysaccharides are (A) Polymers (B) Acids (C) Proteins (D) Oils

Last Answer : (A) Polymers

The pentose sugar present mainly in the heart muscle is (A) Lyxose (B) Ribose (C) Arabinose (D) Xylose

Description : The pentose sugar present mainly in the heart muscle is (A) Lyxose (B) Ribose (C) Arabinose (D) Xylose

Last Answer : (A) Lyxose

A pentose sugar is (A) Dihydroxyacetone (B) Ribulose (C) Erythrose (D) Glucose

Description : A pentose sugar is (A) Dihydroxyacetone (B) Ribulose (C) Erythrose (D) Glucose

Last Answer : (B) Ribulose

A triose sugar is (A) Glycerose (B) Ribose (C) Erythrose (D) Fructose

Description : A triose sugar is (A) Glycerose (B) Ribose (C) Erythrose (D) Fructose

Last Answer : (A) Glycerose

The aldose sugar is (A) Glycerose (B) Ribulose (C) Erythrulose (D) Dihydoxyacetone

Description : The aldose sugar is (A) Glycerose (B) Ribulose (C) Erythrulose (D) Dihydoxyacetone

Last Answer : (A) Glycerose

The general formula of polysaccharides is (A) (C6H10O5)n (B) (C6H12O5)n (C) (C6H10O6)n (D) (C6H10O6)n

Description : The general formula of polysaccharides is (A) (C6H10O5)n (B) (C6H12O5)n (C) (C6H10O6)n (D) (C6H10O6)n

Last Answer : (A) (C6H10O5)n

general formula of monosaccharides is (A) CnH2nOn (B) C2nH2On (C) CnH2O2n (D) CnH2nO2n

Description : general formula of monosaccharides is (A) CnH2nOn (B) C2nH2On (C) CnH2O2n (D) CnH2nO2n

Last Answer : (A) CnH2nOn

. A and B are stereoisomers. They are nonsuperimposable and are mirror images of one another. Which of the following best describes the relationship between A and B? (a) structural isomers (b) enantiomers (c) cis-trans isomers (d) diastereomers

Description : . A and B are stereoisomers. They are nonsuperimposable and are mirror images of one another. Which of the following best describes the relationship between A and B? (a) structural isomers (b) enantiomers (c) cis-trans isomers (d) diastereomers

Last Answer : enantiomers

Which is the reference carbon atom in sugars?

Description : Which is the reference carbon atom in sugars?

Last Answer : Penultimate carbon atom.

Two compounds have the same composition and also have the same atoms attached to the same atoms, although with different orientations in space. These compounds are (a) Identical (b) Position isomers (c) Structural isomers (d) Stereoisomers

Description : Two compounds have the same composition and also have the same atoms attached to the same atoms, although with different orientations in space. These compounds are (a) Identical (b) Position isomers (c) Structural isomers (d) Stereoisomers

Last Answer : Stereoisomers

Which of the statements is correct about diastereomers? (a) They are stereoisomers that are not enantiomers. (b) They are a pair of identical isomers. (c) They are a pair of isomers that are mirror images. (d) All their asymmetric centers are the same.

Description : Which of the statements is correct about diastereomers? (a) They are stereoisomers that are not enantiomers. (b) They are a pair of identical isomers. (c) They are a pair of isomers that are mirror images. (d) All their asymmetric centers are the same.

Last Answer : They are stereoisomers that are not enantiomers

Ethanol (CH3CH2OH) and dimethyl ether (CH3OCH3) are best considered : (a) structural isomers (b) stereoisomers (c) enantiomers(d) diastereomers

Description : Ethanol (CH3CH2OH) and dimethyl ether (CH3OCH3) are best considered : (a) structural isomers (b) stereoisomers (c) enantiomers (d) diastereomers

Last Answer : structural isomers

"Mirror-image" molecules are called: w) stereoisomers x) structural isomers y) diastereomers z) constitional isomers

Description : "Mirror-image" molecules are called: w) stereoisomers x) structural isomers y) diastereomers z) constitional isomers

Last Answer : ANSWER: W -- STEREOISOMERS

Anomers of D-glucopyranose differ in their stereochemistry at __________. (a) C1 (b) C2 (c) C3 (d) C4

Description : Anomers of D-glucopyranose differ in their stereochemistry at __________. (a) C1 (b) C2 (c) C3 (d) C4

Last Answer : C1

Total number of stereoisomers possible for the given structure excluding the configuration mentioned is :

Description : Total number of stereoisomers possible for the given structure excluding the configuration mentioned is :

Last Answer : Total number of stereoisomers possible for the given structure excluding the configuration mentioned is :

What is the possible number of optical isomers for a compound containing 2 dissimilar asymmetric carbon atoms? (a) 2 (b) 4 (c) 6 (d) 8

Description : What is the possible number of optical isomers for a compound containing 2 dissimilar asymmetric carbon atoms? (a) 2 (b) 4 (c) 6 (d) 8

Last Answer : 4

What is the possible number of optical isomers for a compound containing n dissimilar asymmetric carbon atoms? (a) n2 (b) 2n (c) n + 1(d) n + 2

Description : What is the possible number of optical isomers for a compound containing n dissimilar asymmetric carbon atoms? (a) n2 (b) 2n (c) n + 1 (d) n + 2

Last Answer : 2n

Total number of optical active stereoisomers of the following compound is : `CH_(3)-CH=CH-CHCI-CH=C=CH-CH=CH-CH_(3)`

Description : Total number of optical active stereoisomers of the following compound is : `CH_(3)-CH=CH-CHCI-CH=C=CH-CH=CH-CH_(3)`

Last Answer : Total number of optical active stereoisomers of the following compound is : `CH_(3)-CH=CH-CHCI-CH=C=CH-CH=CH-CH_(3)` A. 8 B. 6 C. 16 D. 10

Optical isomers of all aminoacids exist except (A) Glycine (B) Arginine (C) Alanine (D) Hydroxy proline

Description : Optical isomers of all aminoacids exist except (A) Glycine (B) Arginine (C) Alanine (D) Hydroxy proline

Last Answer : Answer : A