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Books Doubtnut Question Bank
BIOMOLECULES
Illustration
α − D -gluocose at C , and C
− 2, C − 3 − 4(OH ) groups.
mutarotation.
∣ ∣
(b). H OCH
5H IO4
2
− C − (CH OH ) − CH2 Oh −−−→
3
zn / ACOH
does it prove?
case?
(Given : 20gmL
−1
of starch has an osmotic pressure
−2 ∘
= 10 atmat25 C. )
glucose is + 19
∘
and the specific rotation of the constant
mixture.
R R'
dipeptide?
⎛ ⎞
(A) ⎜
⎜ N H2 − C H − COOH ⎟
⎟ ,
∣
⎝ ⎠
R
⎛ ⎞
(B) ⎜ ⎟
⎜ N H2 − C H − COOH ⎟ , and
∣
⎝ ⎠
R'
⎛ ⎞
(C) ⎜ ⎟
⎜ N H2 − C H − COOH ⎟ . (X) and reaction with
∣
⎝ ⎠
R'
N H2 N H2 gives a dipeptide (Y ) and amino acid (B).
strand?
aldehyde H3 C(CH2 ) CH O
7
and an aldehyde
monocarboxylic acid OH C(CH2 ) COOH
7
. Write down the
of the fat.
Solved Examples
1. Convert D -glucopyranose to 2, 3, 4 − triethyl
gluocopynoside.
(i)
(ii)
(ii)
formation.
∘
|α| ofD − glu cos e = 52.7
D
∘
|α| ofD − uc → se = − 92.4
D
pyridinol?
(i)
(ii)
Which pair out of (B) and (E) gives meso-acids (C) and (F )
Given, (A) does not reduce Fehling's solution and does not
mutarotate.
reaction conditions?
behaviour of alanine in H 2
O .
isoelectric point.
point?
c. Transcription, d. Translation
e. Codond
and RN A?
carbohydrates.
artery?
synthesis.
fructose,and lactose.
lactose?
cellulose?
following reagents?
(i). H I
(ii).Bromine water
(iii). H N O 3
(iii)Denaturation
proteins?
structure of proteins?
acids?
proteins?
20. Why are vitamin A and vitamin C essential for us? Give
functions.
complementary. Explain.
1.
A. Methyl− α − D − glucofuranoside
B. Methyl− β − D − glucofuranoside
C. Methyl− α − D − glucopyranoside
D. Methyl− β − D − glucopyranoside
Answer: C
2.
reaction is:
A. One
B. Two
C. Three
D. Four
Answer: B
3.
A.
B.
C.
D.
Answer: A
A.
B.
C.
D.
Answer: A
A. Methyl-α-D-glucofuranoside
B. Methyl-β -D-glucofuranoside
C. Methyl-α-D-glucopyranoside
D. Methyl− β − D − glucopyranoside
Answer: A
reaction is:
A. One
B. Two
C. Three
D. Four
Answer: B
A.
B.
C.
D.
Answer: C
8.
A.
B.
C.
D.
Answer: B
9.
Answer: B::C::D
10.
B.
C.
Answer: C
A.
B.
C.
D. All
Answer: C
Watch Video Solution
12.
A.
B.
C.
13.
and (F )?
Answer: A::D
linkage.
linkage.
Answer: B::D
15.
A.
B.
C.
Answer: C
A.
B.
C.
D. All
Answer: C
17.
B.
C.
Answer: D
Answer: A::D
19.
B. Osazone (A)
C. Both
D. None
Answer: A
20.
B. 2
C. 3
D. 4
Answer: A
21.
B. Osazone of (C )
C. Both
D. None
Answer: B
22.
B. 3
C. 2
D. 1 / 3
Answer: D
23.
B. Leu → Val
C. Gly → Ala
D. Ala → Gly
Answer: A
24.
Answer: B
25.
Answer: D
26.
A. 1
B. 2
C. 3
D. 4
Answer: C
27.
A.
B.
C.
D.
Answer: A
28.
B.
C.
D.
Answer: B
A.
B.
C.
Answer: A
structure as H a b c
, H , H andH
d
)
A. H a
B. H b
C. H c
D. H d
Answer: C
31.
A. 1
B. 2
C. 3
D. 4
Answer: B
32.
five-membered ring.
six-membered ring.
Answer: C::D
33.
A. It is a γ -lactone.
B. It is a δ-lactone
Answer: A::C
34.
represented as:
A.
B.
C.
D.
Answer: C
A. Diastereomers
B. Anomers
C. C − 2 epimer
D. C − 3 epimer
Answer: A::C
A. Wohl's method
B. Ruff method
C. Kilian's method
D. Ekenstein method
Answer: C
A. Both γ -lactones
B. Both δ-lactones
D. None
Answer: A
A.
C.
Answer: A
Answer: C::D
Watch Video Solution
D. α − D( + ) glucopyranose and β − D( + )
Answer: A::B::C
form osazone.
to form osazone.
P hN H N H2 to form phenylhydeazone.
P hN H N H2 to form osazone.
Answer: B::C::D
amino acids.
configuration.
acidic groups is ( − N H 3
.
)
Answer: B::C::D
A. Glucose
B. Maltose
C. Frctose
D. Galactose
Answer: A::B::C::D
α − D( + ) glucopyranose.
B. Invert sugar is laevorotatory.
Answer: A::B::C::D
C. Glycosides mutarotate.
is / are :
A. D-glyceraldehyde
B. D-Erythrose
C. D-Threose
D. D-Ribose
Answer: B::C
Answer: A::D
Answer: A::B::C
diasteremers.
Answer: A::B::C::D
B.
C.
D.
Answer: A::B::D
B. Glucose, Mannose
C. Glucose, Indose
D. Galactose, Talose
Answer: A::B::C::D
A. Glucose, Fructose
B. Glucose, Mannose
C. Ribose, Arabinose
D. Mannos4e, Fructose
Answer: A::B::C::D
enantiomers?
Answer: A
A. (C1
− α)(OH ) of glucopyranose is linked with
(C2 ( − β ) ( OH )
of fructofuranose.
B. (C1
− α)(OH ) of glucopyranose is linked with
D. It exhibits mutarotation.
Answer: A
fructofuranside.
glucopyranoside.
Answer: A::B::C::D
a hexaacetate product.
octa-acetate product.
Answer: A::D
A. (C1
− β)(OH ) of glucose is linked with (C 4
− OH ) of
galactose.
B. (C1
− β) − (OH ) of galactose is linked with
(C4 − OH ) of β -glucose.
D. It exhibits mutarotation.
Answer: B::D
glucopyranoside.
galactopyranoside
C. On methylation with M eOH / H Cl , it gives methyl-β -
D-glactopyranosyl- β -D-glucopyranoside.
D-glucopyranosyl-β -D-galactopyranoside.
Answer: A::B::C
lactose?
A. The product (C ) is methyl-hepta-o-methyl- β -D-
galactopyranosyl-β -D-glucopyranoside.
galactopyranosyl-β -D-glucopyranoside.
Answer: A::C
maltose?
A. Product (C ) is :
B. Product (C ) is :
Answer: A::D
23. How many base pairs in the gene are needed to code for
egg white?
A. 3 × 129
D. 4 × 129
Answer: B
Watch Video Solution
A. Oxytocin
B. Vasopressin
C. Insulin
D. Haemoglobin
Answer: A::B::C
B. Muscles
C. Keratin
D. Blood
Answer: A::D
group on L.H.S.
( − N H2 ) group on L.H.S.
laevoratotory.
Answer: A::B
proteins are pI of (A), (B), and (C) which are 1.1, 6.7 , and
Answer: A::B::C
Answer: A::C::D
View Text Solution
⎛ ⎞
⎜ H OOC −
⎜ CH − CH2 COOH ⎟
⎟ (A)The pK a1 , pKa2 ,
∣
⎝ ⊕ ⎠
. N H3
⎛ N H3 ⎞
∣
⎜ ⎟
⎜ R C H − COOH ⎟
⎜ ⎟
⎜ ⎟
⎝ ⎠
pKa + pKa
A. 1 2
pKa1 + pKa3
B.
2
pKa2 + pKa3
C.
2
pKa1 + pKa2 + pKa3
D.
3
Answer: A
⎛ ⎞
⊕
pKa1 + pKa2
A.
2
pKa1 + pKa3
B.
2
pKa2 + pKa3
C.
2
pKa1 + pKa2 + pKa3
D.
3
Answer: C
anomers.
reducing sugar.
Answer: A::B::C::D
A. Ether linkage
B. Ester linkage
C. Peptide llinkage
Answer: C
A. Polysaccharides
B. Polypeptides
C. Polypeptides
Answer: B
A. Monoacetate
B. Tetra-acetate
C. Penta-acetate
D. Hexa-acetate
Answer: C
found in an enzyme?
A.
B.
C.
D.
Answer: C
A. Transport oxygen
B. Provide immunity
D. Provide energy
Answer: C
Answer: B
A. Three
B. Two
C. One
D. Four
Answer: A
8. Vitamin A is called:
A. Ascorbic acid
B. Retinol
C. Calciferol
D. Tocopherol
Answer: B
cells?
A. Starch
B. Cellulose
C. Sucrose
D. Vitamins
Answer: B
body is:
A. Thyroxine
B. Adrenaline
C. Insulin
D. Cortisone
Answer: C
A. Chlorophyll
B. Haemocyanin
C. Carbonic abhydrase
D. Vitamin B 12
Answer: A
A. Riboflavin
B. Cobalalmin
C. Thiamine
D. Pyridoxine
Answer: B
A. Scurvy
B. Rickets
C. Pyrrohea
D. Pernicious anaemia
Answer: A
A. Enantiomers
B. Geometrical
C. Epimers
D. Anomers
Answer: D
Answer: A
A. Three
B. Four
C. Five
D. Six
Answer: D
A. It is optically inactive.
C. It is a dicarboxylic acid
Answer: A
(CO − N H ) group.
Answer: A
are:
A. A, D
B. A, B
C. A, C
D. D, B
Answer: A
A. − COOH
B. − N H 2
C. − CH 3
Answer: D
A. L-Glucose
B. D-Fructose
C. D-Ribose
D. D-Glucose
Answer: D
operation of:
A. Electrostatic attractions
C. Dipole-dipole interactions
D. Hydrogen bonding
Answer: D
cytosine (C).
guanine (G).
Answer: A
Watch Video Solution
A. 2
B. 3
C. 4
D. 5
Answer: C
B. Methylglycine
C. 2-Hydroxymethylserine
D. Tryptophan
Answer: C
glycogen is:
A. Cortisone
B. Bile acids
C. Adrenaline
D. Insulin
Answer: D
A. Maltose
B. Lipase
C. Zymase
D. Pepsin
Answer: B
Watch Video Solution
is that it
Answer: C
chain?
N O
∣ ∣ ∣ ∣
A. − N − C − H − C − NH − C − NH −
∣ ∣ ∣ ∣
O H
H H O
∣ ∣ ∣ ∣ ∣ ∣ ∣ ∣
B. − N − C − C − C − C − N − C − C −
∣ ∣ ∣ ∣ ∣ ∣
H H O
∣ ∣ ∣ ∣ ∣ ∣
C. − N − C − C − N − C − C −
∣ ∣ ∣ ∣
D.
H O H
∣ ∣ ∣ ∣ ∣ ∣ ∣ ∣ ∣ ∣
−N − C − C − C − N − C − C − N − C − C − C −
∣ ∣ ∣ ∣ ∣ ∣ ∣ ∣ ∣
H O
Answer: C
A. 5
B. 6
C. 3
D. 4
Answer: A
A. Dipeptide bonds
B. Hydrogen bonds
C. Ether bonds
D. Peptide bonds
Answer: B
A. A coenzyme
B. A hormone
C. An enzyme
D. An antibiotic
Answer: B
A. Uracil
B. Cytosine
C. Guanine
D. Thymine
Answer: A
A. Thymine
B. Cytosine
C. Guanine
D. Thymine
Answer: C
polysaccharide:
A. Starch
B. Glucose
C. Glycogen
D. Galactose
Answer: C
molecule is:
A. Relication
B. Mutation
C. Duplication
D. Dislocation
Answer: B
( − OH ) group around:
A. C
1
B. C
2
C. C
3
D. C
4
Answer: A
A. Thioether
B. Thiol
C. Thioester
D. Thiolactone
Answer: B
B. C2
and C5 , respectively, of the sugar molecule.
C. C1
and C5 , respectively, of the sugar molecule.
D. C5
and C1 , respectively, of the sugar molecule.
Answer: C
A. α − Keratin
B. Hyaemoglobin
C. Ribonuclease
D. Aldenine
Answer: A
synthesis (translation)?
attachment.
Answer: B
A. Enzymes
B. DNA
C. Vitamins
D. Hormones
Answer: C
−−−−−−→ Polypeptides
Answer: D
45. The pair in which both the species have iron is:
A. Nitrogenase, cytochromes
B. Carboxypeptidase, haemoglobin
C. Haemoglobin, nitrogenase
D. Haemoglobin, cytochromes
Answer: D
A. 5 − Methyluracil
B. 4 − Methyluracil
C. 3 − Methyluracil
D. 1 − Methyluracil
Answer: A
Watch Video Solution
A. 3 to 4
B. 5 to 6
C. 6 to 7
D. 8 to 9
Answer: D
glucoside are:
A. Epimers
B. Anomers
C. Enantiomers
D. Conformational diastereomers
Answer: B
⊕ Θ
A. H 3
N − CH2 COO
B. H 3
N − CN2 COOH
C. H 2
N CH2 COOH
D. H 2
N CH2 COO
Answer: B
known as:
A. Vitamin H
B. Vitamin B 1
C. Vitamin B 12
D. Vitamin D
Answer: A
molecules.
reaction.
Answer: A
A. Glucosazone
B. Glucose phenylhydrazone
C. Glucose oxime
D. Sorbitol
Answer: A
C. Enantiomers of glucose.
carbon one (C − 1)
Answer: D
Answer: C
galactose.
Answer: B
only:
A. D − Glucose units joined by α − glycosidic linkage.
Answer: B
A. lysine
B. Histidine
C. Valine
D. Alanine
A. Glucose+Glucose
B. Glucose+Galactose
C. Glucose+Fructose
D. Glucose+Lactose
Answer: C
is:
A. Proline
B. Tyrosine
C. Valine
D. Tryptophan
Answer: D
A. Adrenaline
B. Esterone
C. Cortisone
D. Testosterone
Answer: B
sepentina is:
A. Aspirin
B. Quinine
C. Bithional
D. Reserpine
Answer: D
A. Heteroauxin
B. Gibberrellins
C. Cytokinnis
Answer: D
A. Cat
B. Dog
C. Gypsy moth
D. Human
Answer: C
A. Centrifuge
B. Chromatograph
C. Mass spectometer
D. Electrolytic cell
Answer: B
A. Glucose
B. Sucrose
C. Glycogen
D. Cellulose
Answer: D
carbon chain in an
A. Alcohol
B. Alkene
C. Ketose
D. Aldose
Answer: D
chain in:
A. Acid
B. Alcohol
C. Aldose
D. Ketose
Answer: C
enantiomers.
epimers.
Answer: A
contain nitrogen.
Answer: A
sequence in DN A.
proteins.
Answer: D
hypoglycemia.
sugar level.
Answer: C
Answer: A
A. Natural rubber
B. Vitamin A
C. Terpenes
D. Vitamin E
Answer: D
called the:
A. Eutectic point
B. Neutralisation point
C. Effusion point
D. Isoelectric point
Answer: D
produces:
A. 2AT P molecules
B. 50AT P molecules
C. 38AT P molecules
D. 36AT P molecules
Answer: C
A. Phosphoric acid
B. Fatty acid
C. Bile acids
A. T ACT GACAG
B. T U CT GU CCU G
C. GU AGT U AU G
Answer: A
A. m − RN A
B. r − RN A
C. t − RN A
Answer: D
A. It is a nucleotide.
B. It contains the purine adenine.
Answer: C
A. Primary structure
B. Secondary structure
C. Tertiary structure
D. Quaternary structure
Answer: A
Exercises (Assertion-Reasoning)
Answer: D
form.
A. Statement I is true, Statement II is true, Statements
Answer: A
reagent.
Answer: D
Answer: A
Answer: D
Answer: A
atoms.
Answer: D
not enzymes.
Answer: A
boiling with Aq. N aOH gives solid cake with soapy touch.
reactions.
Answer: C
realations.
oxygen.
Answer: C
Answer: C
Answer: C
Answer: D
Answer: A
Ekenstein rearrangement.
Answer: A
A. Glucose, Sucrose
B. Glucose, fructose
C. Hexanal, acetophenone
D. Fructose,sucrose
Answer: B
A. Isomer
B. Anomer
C. Epimer
D. Enantiomer
Answer: B
B.
C.
D.
Answer: A
Answer: A
sugar.
sugar.
respectively.
D. The glucosidic linkages in (X) and (Y ) are β and α ,
respectively.
Answer: B::C
Answer: C
reactions:
(i)
(ii)
following structure:
hydrolysis of aspartame.
polymerisation of ethylene.
Tollens reagent?
QUESTION BANK
RNA are
disaccharides?
(II) Nylon-6
(III) Teffon
(IV) Terylene
polymerisation?
(I) Nylon-6,6
(II) Terylene
(III) Bakelite