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The document discusses various aspects of carbohydrates and proteins, including their classifications, structures, and reactions. It covers topics such as reducing and non-reducing sugars, glycosidic linkages, and the properties of amino acids and proteins. Additionally, it poses questions related to these topics, emphasizing the importance of carbohydrates and proteins in biological systems.
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10.1 Carbohydrates
nt
Lille]
‘Assertion (A) : Fructose is a reducing sugar.
Reason (R) : Fructose does not reduce Fehling
solution and Tollens’ reagent.
(a) Both Assertion (A) and Reason (R) are true and
Reason (R) is the correct explanation of the
Assertion (A).
(&) Both Assertion (A) and Reason (R) are true but
Reason (R) is not the correct explanation of the
Assertion (A).
(©) Assertion (A) is true, but Reason (R) is false.
(d) Assertion (A) is false, but Reason (R) (Q))
is true. (2024) (ip)
Assertion (A) : D(+)-Glucose is dextrorotatory.
Reason R): Symbol'D’ representsits dextrorotatory
nature.
(a) Both Assertion (A) and Reason (R) are true and
Reason (R) is the correct explanation of the
Assertion (A).
(b) Both Assertion (A) and Reason (R) are true, but
Reason (R) is not the correct explanation of the
Assertion (A).
(c) Assertion (A) is true, but Reason (R) is false.
(a) Assertion (A) is false, but Reason (R) is true.
(2023C)
Which of the following is a non-reducing sugar?
(a) Sucrose (b) Maltose
(©) Glucose (@) Lactose (2023) (U)
The glycosidic linkage involved in linking the glucose
Units in amylose part of starch is
(a) Cy—Cgatlinkage (b) C;—C,,B linkage
(c) Cy—Cgalinkage (d) Cy —CgB linkage
(2023)
Which of the following sugar is known as dextrose?
{a) Glucose (b) Fructose
(c) Ribose (d) Sucrose
(Term |, 2021-22)
a-D(+) glucose and f-D(+) glucose are
(a) geometrical isomers (b) enantiomers
(c) anomers (d) optical isomers.
(2020) (i)
Assertion (A) : Sucrose is a non-reducing sugar.
Reason (R) : Sucrose has glycosidic linkage.
{a) Both Assertion (A) and Reason (R) are correct
statements, and Reason (R) is the correct
explanation of the Assertion (A).
BsWiee
CBSE Champion Chemistry Class 19
(b) Both Assertion (A) and Reason (R) are correct
statements, but Reason (R) is not the correct
‘explanation of the Assertion (A).
(c) Assertion (A) is correct, but Reason (R) is
incorrect statement.
(d) Assertion (A) is incorrect, but Reason (R) is
correct statement. (2020) (in)
= (1mark)
‘Name the disaccharide which on hydrolysis gives
two molecules of glucose. (One word, 2020)
9. Write the name of linkage joining two
monosaccharides. (One word, 2020)
410, What is the basic structural difference between
glucose and fructose? (Delhi 2019) )
Write the structural difference between starch and
cellulose. (Al 2019, 2016)
Write the products obtained after hydrolysis of
lactose. (Delhi 2019)
11.
12.
OR
Write the name of two monosaccharides obtained
‘on hydrolysis of lactose sugar. (Delhi 2016)
Name a carbohydrate present in liver, muscles and
brain (2019C)
What are the hydrolysis products of sucrose ?
(2019C)
13.
14,
Define the following with an example
Polysaccharides (1/3, 2018)
Write the product when D-glucose reacts with cone
HNO3. (1/3, 2018)
‘Which one of the following is a disaccharide: Starch.
Maltose, Fructose, Glucose? (Delhi 2015) 60)
Write the product obtained when D-glucose reacts
with HJN—OH. (al 2015)
Which one of the following is a monosaccharide
starch, maltose, fructose, cellulase (Foreign 2015) (U
15.
16.
17.
18.
19.
! (2 marks)
20. Classify the following sugars into monosaccharides
and disaccharides : Fructose, Lactose,
Glucose, Maltose. (2024)
Give the reaction of heating glucose with
hydroxylamine. Presence of which group |=
21.
ee
confirmed by this reaction? (2023) (Au)
22, Define the following terms
(i) Oligosaccharides .
(il) Invert sugar (2020)(R) |
ee
PBiomolecules
ja, Write the reactions showing the presence of
following in the open structure of glucose
(i) analdehyde group
(i) a primary alcohol
SEMIN (3 marks)
24, (a) What are the hydrolysis products of (i) Lactose,
(i) Maltose?
(b) Give the basic structural difference between
(2020)
starch and cellulose. (2023)( 1°)
25, Write the reaction of glucose with
() HEN (i) Bry Gi) HI (2021 ¢)
26. Write chemical reactions to show that open
structure of D-glucose contains the following :
(i) Straight chain
(i) Five alcohol groups
(i) Aldehyde as carbonyl group. (Dethi 2019) (U']
What happens when D-glucose is treated with the
following reagents?
(a) Br, water (b) HN
(0 (CHyCO),0 (al2019)
(4 marks)
Case Based Questions
for life in both
28, Carbohydrates are essential
plants and animals. Carbohydrates are used as
storage molecules as starch in plants and glycogen
in animals. Chemically they are polyhydroxy
aldehydes or ketones. On the basis of their
behaviour on hydrolysis, carbohydrates are
classified as monosaccharides, oligosaccharides and
polysaccharides. All monosaccharides are reducing
sugars, ie,, they are oxidized by Tollens’ reagent and
Fehling's solution, A monosaccharide like glucose is
aldohexose and its molecular formula was found to
be CyHy20,, After reacting with different reagents
like HI, HJN—OH, bromine water, (CH3CO),0, ete.
its structure was found to contain one aldehyde
Broup, one primary alcoholic group, (-CH7OH) and
four secondary alcoholic groups (»CHOH). Despite
having the aldehyde group, glucose does not give
some of the reactions of aldehyde group like Schiff's
test, NaHSO; addition. This explains the existence
of glucose in two cyclic hemiacetal forms which
difer ony inthe configuration of the hydroxyl group
Answer the following questions :
(a) What are reducing sugars?
(6) Classify the following into monosaccharide and
disaccharide :
Fructose, Sucrose, Lactose, Galactose
(0 Name the polysaccharide which is known as
‘animal starch: Why is it called ‘animal starch’?
30.
297
OR
() () Name the isomers of glucose which in the
cyclic form differ only in the configuration
of the -OH group at C-1.
(ii) Presence of which functional
group was detected when glucose
reacted with Br, water?
Carbohydrates are the major components of all
living organisms. Sugars are carbohydrates. The
major types of sugars include monosaccharides
and disaccharides. The main difference between
monosaccharides, disaccharides and polysaccharides
is that monosaccharides are monomer of sugars
and disaccharides are composed of two monomers,
whereas polysaccharides are composed of a large
number of monomers. Monosaccharides are single
sugar molecules which act as the building blocks of
disaccharides and polysaccharides. Disaccharides
are also simple sugars. Disaccharides are classified
intotwo groups according to their reducingstrength
Reducing and Non-reducing sugars. When a polymer
is formed from a monomer, a condensation reaction
occurs that forms a glycosidic bond and water
molecule is lost. Starch, glycogen and cellulose are
examples of polysaccharides. Starch is found in
many parts of plant cell and consists of amylose and
amylopectin. Glycogen is the major carbohydrate
storage product found in humans. It is present
in liver, muscles and brain. Cellulose is the most
abundant organic molecule on Earth, It makes up
around 50% of all organic carbon.
Answer the following questions :
(a) Name the linkage which
monosaccharide units in polysaccharides.
(b) Carbohydrates are classified on the basis of their
behaviour on hydrolysis. Write the hydrolysis
products of sucrose.
() Write two differences between amylose and
amylopectin.
(2024) CBQ
connects
OR
(o) (i). What are reducing sugars?
(ii) Sucrose is dextrorotatory but the mixture
obtained after hydrolysis is laevorotatory.
Why? (2023¢)
Carbohydrates are optically active polyhydroxy
aldehydes and ketones. They are also called
saccharides. All those carbohydrates which reduce
Fehling’s solution and Tollens’ reagent are referred
to as reducing sugars. Glucose, the most important
source of energy for mammals, is obtained by
the hydrolysis of starch. Vitamins are accessory
food factors required in the diet. Proteins are the
polymers of a-amino acids and perform various298
structural and dynamic functions in the organisms.
Deficiency of vitamins leads to many diseases.
Answer the following :
(a) The pentaacetate of glucose does not react with
hydroxylamine. What does it indicate?
(b) Why cannot vitamin C be stored in our body?
(c)_ Define the following as related to proteins
(i) Peptide linkage
(ii) Denaturation
OR
(c)_ Define the following as related to carbohydrates :
(i) Anomers
(ii). Glycosidic linkage (2023)
10.2 Proteins
L Mico
35.
36,
37.
38.
The specific sequence in which amino acids are
arranged in a protein is called its
(a) primary structure
(b) secondary structure
(c) tertiary structure Q a
(d) quaternary structure (2024)(R)
{pleated sheet structure in proteins refers to
(a) primary structure (b) secondary structure
(©) tertiary structure (d) quaternary structure.
(2023)
‘An achelix i a structural feature of
(a) sucrose (b) polypeptides
(©) nucleotides (4) starch. (2023, 2020)
Complete the following analogy :
Curdling of milk : A:: a-helix : B
(a) A: Primary structure ,B : Secondary structure
(b) A: Denatured protein, B : Primary structure
(©) A: Secondary structure, B : Denatured protein
(d) A: Denatured protein, B : Secondary structure
(Term 1, 2021-22) (An)
‘Amino acids which cannot be synthesized in the
body and must be obtained through diet are known as
(a) acidic amino acids
(b) essential amino acids
(c)_ basic amino acids
(d) non-essential amino acids. (Term I, 2021-22)
The helix structure of proteins is stabilised by
(a) peptide bond (b)_ hydrogen bond
(©) disulphide bond (d)_ van der Waals’ forces.
(2021C)
Peptide linkage is present in
(a) carbohydrates (b) vitamins
(c) protein (4) rubber. (2020)(1!)
Amino acids are
(a) acidic (b) basic
(c) amphoteric (d) neutral. (2020)(f1]
(IEZED CRSE Champion Chemistry Class 19
39. Assertion (A) : Albumin is a globular protein,
Reason (R) : Polypeptide chain coils around to give
a straight chain
(a) Both assertion (A) and reason (R) are correct
statements, and reason (R) is the correct
explanation of the assertion (A).
(b) Both assertion (A) and reason (R) are correct
statements, but reason (R) is not the correct
explanation of the assertion (A)
(©) Assertion (A) is correct, but reason (R) is
incorrect statement.
(d) Assertion (A) is incorrect, but reason (R) is
correct statement. (2020)
(1 mark)
40. What is the difference between a glycosidic linkage
and a peptide linkage ? (2019) 0)
41. Define the following terms with a suitable example
of each:
(a) Anomers
(b) Essential amino acids
() Denaturation of protein (2019)
42. What is the difference between fibrous protein and
globular protein? (1/3, Al 2017C, Delhi 2015)
43. Give one example each for fibrous protein and
globular protein. (Al 2016)
44, Amino acids show amphoteric behaviour. Why?
(al 2015) in)
45. What is the difference between acidic amino acids
and basic amino acids? (Foreign 2015)
BEND (2 marks)
46. Define the following terms
{a) Denaturation of protein Qe
(b) Invert sugar (2024) 8
47. Define denaturation of protein. What is the effect of
denaturation on the structure of protein? (2023)
48, (a) Write chemical reaction to show that open
structure of D-glucose contains the straight chai.
(b) What type of linkage is responsible for the
formation of protein? (2023) (An
49. Define the following with an example of each
() Denatured protein
(ii) Essential amino acids (2/3, 2018)
50. (a) Amino acids show amphoteric behaviour. Why?
(b) Write one difference between a-helix and
[pleated structures of proteins, (2/3, 2018)
HEMI (3 marks)
51. Define the following terms
(a) Glycosidic linkage
(b) Primary structure of protein
() Disaccharides
eeesiomolecules
(a) Write the product when D-glucose reacts with
conc. HNO3,
{v) Amino acids show amphoteric behaviour. Why?
() Write one difference between achelix and
frpleated structure of protein. (2023)
Define proteins and classify them on the basis of
their molecular shape. (2020¢)
_. Differentiate between the following :
(i) Amylose and Amylopectin
{i) Peptide linkage and Glycosidic linkage
{ii) Fibrous proteins and Globular proteins,
(Delhi 2019) (Ev)
Define the following terms as related to proteins :
(i) Peptide linkage (ii) Primary structure
(iii) Denaturation (Al 2015)
BEE 6 aris) =
Case Based Questions
56. Read the given passage and answer the questions
number (i) to (v) that follow : 1x5=:
Organic compounds containing amine as functional
group are present in a vivid variety of compounds,
namely amino acids, hormones, neurotransmitters,
DNA, alkaloids, dyes, etc. Drugs including nicotine,
morphine, codeine and heroin, etc. which have
physiological ettects on humans also contain: amino
group in one form or another. Amines are basic
because of the presence of lone pair of electrons
on nitrogen. Addition of nitrogen into an organic
framework leads to the formation of two families of
molecules, namely amines and amides. As chemistry
students, we must appreciate the versatility of
nitrogen,
(i) What are amino acids ?
(ii) Why are amino acids amphoteric ?
(iii) Give one point of difference between acidic and
basic amino acid.
{iv) What are essential amino acids ?
(V) Name the linkage formed when carboxyl end
of one amino acid condenses with amino end of
other amino acid. (2020)
10.4 Vitamins
ra
57. Whi
7. Which of the following acids represents vitamin C?
(a) Saccharic acid (b) Gluconic acid
(0) Ascorbic acid @
(2024)
(d) Benzoic acid
WW mark)
5
8. Why vitamin C cannot be stored in our body?
(Delhi 2016)
59, Writ
le the name of vitamin whose deficiency causes
ne deformities in children. (Delhi 2015)
299
60. Write the name of the vitamin whose deficiency
causes bleeding of gums. (Foreign 2015)
HMB (2 marks)
61. Define vitamins and classify them on the basis of
(2020C) fi
their solubility.
HEMI (3 marks)
62. (a) What are the products of hydrolys’s of maltose ?
(b) What type of bonding provides stability to
a-helix structure of protein ?
(c) Name the vitamin whose deficiency causes
pernicious anaemia. (2019)
63. How are vitamins classified? Name the vitamin
responsible for the coagulation of blood./Delhi 2015C)
(4 marks)
Case Based Questions
64, Certain organic compounds are required in
small amounts in our diet but their deficiency
causes specific disease. These compounds are
called vitamins. Most of the vitamins cannot be
synthesised in our body but plants can synthesised
almost all of them. So they are ccnsidered as
essential food factors. Howevers. the bacteria of
the gut can produce some of the vitamins required
by us. All Lite vitamins are generally available in our,
diet. The term ‘vitamin’ was coined from the words
vital + amine, since the earlier identified compounds
had amino group. Vitamins are classified into two
groups depending upon their solubility in water or
fat namely-fat soluble vitamins and water soluble
vitamins.
‘Answer the following questions
(a) What is the other name of vitamin B,?
(b) Name the vitamin whose deficiency causes
increased blood clotting time.
() Xerophthalmia is caused by the deficiency of
which vitamin ? Give two sources of this vitamin.
OR
(c) Why can't vitamin C be stored in our body?
Name the disease caused by the
deficiency of this vitamin.
10.5 Nucleic Acids
Ie)
65. Assertion (A) : Uracil base is present in DNA.
Reason (R) : DNA undergoes self-replication
(a) Both Assertion (A) and Reason (R) are true and
Reason (R) is the correct explanation of the
Assertion (A).
(b) Both Assertion (A) and Reason (R) are true, but
Reason (R) is not the correct explanation of the
Assertion(A).
2
(2024)300
(c)_ Assertion (A) is true, but Reason (R) is false.
(a) Assertion (A) is false, but Reason (R) @
is true (2024)
Assertion : The backbone of DNA RNA
molecules is a chain consisting of heterocyclic base,
pentose sugar and phosphate group.
Reason ; Nucleotides and nucleosides mainly differ
from each other in presence of phosphate group.
(a) Both Assertion (A) and Reason (R) are true and
Reason (R) is the correct explanation of the
Assertion (A)
(b) Both Assertion (A) and Reason (R) are true, but
Reason (R) is not the correct explanation of the
Assertion (A)
(c) Assertion (A) is true, but Reason (R) is false.
(d) Assertion (A) is false, but Reason (R) is true.
(2023)
and
The base which is present in DNA but not in RNA, is
(a) cytosine (b) guanine (c) adenine (d) thymine.
(Term 1, 2021-22)( A)
Nucleic acids are polymer of
(a) amino acids (b) nucleosides
(c) nucleotides (d)_ glucose.
(Term |, 2021-22, 2021C)
Nucleosides are composed of
(a) apentose sugar and phosphoric acid
(b) anitrogenous base and phosphoric acid
(©) anitrogenous base and a pentose sugar
(@) a nitrogenous base, a pentose sugar and
phosphoric acid.
(Term |, 2021-22) (fi)
areas (1 mark)
Name the unit formed by the attachment of a base
to 1 position of sugar. (2020C)
Write the products obtained after hydrolysis of
DNA. (2019)
What is difference between a nucleoside and
nucleotide? (2019, Delhi 2016)
(HEED CBSE Champion Chemistry lag
55.12
What type of linkage is present in nucleic acids»
(Al 2016)
7.
BEN (2 marks)
74. (a) What happens when glucose reacts with nitric
acid ? Write chemical equation
(b) Write one structural difference Q
between DNA and RNA (2024)
75. Write two differences between DNA and RNA
(2023, 2019)
(3 marks)
76. Give reasons for any 3 of the following observations
(a) Penta-acetate of glucose does not react with
hydroxylamine.
(b) Amino acids behave like salts.
(c). Water soluble vitamins must be taken regularly
indiet.
{d) The two strands in DNA are complementary to
each other. (2023)
Differentiate the following
(i) Fibrous protein and Globular protein
(ii). Essential amino acids and Non-essential amino acids
(iii) DNA and RNA (20210)
Give the plausible explanation for the following
(a) Glucose doesn't give 2.4-DNP test.
(b) The two strands in DNA are not identical but are
complementary.
(c) Starch and cellulose both contain glucose unit
‘as monomers yet they are structurally different.
77.
78.
(2020)
79. Differentiate between following :
(i) Amylose and Amylopectin
(ii), Globular protein and Fibrous protein ra
(2020)
i) Nucleotide and Nucleoside
Define the following terms :
(a) Invert sugar (b) Native protein
(c) Nucleotide
80.
(2019)
a err reece ES MiCc crny,
):Reducing sugars are those which can reduce
solution and Tollens' reagent e.g., Glucose and
Fehling
Fructose.
> {c):Glucose is correctly named as D(+)-glucose. ‘D’
before the name of glucose represents the configuration
wnhereas (+) represents dextrorotatory nature of the
molecule.
2, [a):sSucrose is a non-reducing sugar which on
tydrolysis gives equimolar mixture of o-D(+)-glucose and
p-D(-)fructose. Since, the reducing groups of glucose
and fructose are involved in a glycosidic bond formation
(C1 of arglucose and C2 of B-fructose), hence sucrose is
non-reducing sugar.
4, (c):Starch is main storage polysaccharide of plants.
It is a polymer of a-D-glucose and consists of two
components - Amylose and Amylopectin. Amylose is
held by Cy - Cg a-glycosidic linkage while amylopectin is
formed by a - Cy - Cz and ot - Cy - Cg glycosidic linkage.
5, (2):Glucose is known as dextrose.
6. (cj: The pair of stereoisomers which differ only in
the configuration of the hydroxyl group at C, are called
anomers.
A :
H—C—OH HO——-C——-H
2 2|
H: 7 OH 0 H a OH 3
HO. H HO H
4 4)
H ‘OH H OH
H 5 H 7
6 6
(CH,OH CH,OH
a-D-(+)Glucose -D-(+)Glucose
> Anomers differ in configuration at C-1 only.
7. {a):Sucrose is disaccharide and its two
monosaccharides are held together by aglycosidic linkage.
Since, the reducing groups of glucose and fructose are
involved in glycosidic bond formation, therefore, sucrose
isa non-reducing sugar.
8. Maltose
9. Glycosidic linkage
10. Glucose contains an aldehydic group while fructose
contains a ketonic group.
14. The basic structural difference between starch and
cellulose is of linkage between the glucose units.
In starch, there is o-D-glycosidic linkage. Both the
components of starch-amylose and amylopectin are
polymer of a-D-glucose. On the other hand, cellulose
is a linear polymer of B-D-glucose in which C, of one
glucose unit is connected to C, of the other through
B-D-glycosidic linkage.
42. Lactose on hydrolysis gives -D-glucose and
B-D-galactose,
13. Carbohydrate is present in the form of glycogen in
liver, muscles and brain.
14. Hydrolysis products of sucrose are glucose and
fructose.
15. Carbohydrates which yield a large number
of monosaccharide units on hydrolysis are called
polysaccharides, eg,, cellulose.
16. On oxidation with nitric acid, D-glucose yields
saccharic acid.
CHO for
i} HNO.
(CHOH), —“—" (CHOM,
|
CH,0H COOH
D-glucose D-saccharic acid
amg
> Oxidation of D-glucose takes place in presence of
nitric acid.
17. Maltose is a disaccharide as it consists of two
a-D-glucose units.
18. D-Glucose reacts with H,N—OH to give glucose
oxime.
CHO CH=N—OH
I
(CHOH),+NHjOH —> (CHOH),
CH,OH CH,OH304
c=mmng
‘OTH;N—on #25 Sc=N—on
e
19. Fructose is a monosaccharide because it cannot
be hydrolysed to simpler polyhydroxy aldehydes or
ketones.
20. Monosaccharides : Glucose and fructose
Disaccharides : Lactose and maltose
fies i |=NOH
24. (CHOM)y Moe (CHOH),
i (Conf the presence ofa
4,08 ‘crteny ero) u,0H
Gcmse use oxne
22. (i) These are the carbohydrates which on hydrolysis
give 2-10 monosaccharides. For example, sucrose,
lactose, maltose, etc.
(i) An equimolar mixture of glucose and fructose,
obtained by hydrolysis of sucrose in presence of an acid
or the enzyme invertase is called invert sugar.
23. (i) Glucose on oxidation with a mild oxidising
agent like bromine water gives gluconic acid containing
CBSE Chambon Chemisty Ch
51
the same six carbon atoms as present in glucose. ry,
indicates presence of aldehyde group,
CHO COOH
| Br,/H,0
(HOH +0] —— (CHoH,
CH,OH CHOW
Gluconicaci
Ui) On acetylation with acetic anhydride, glucose ps
a pentaacetate. This confirms that glucose contains fg
OH groups.
CHO CHO 0
(dHom, +5(CH3CO},0 —> a -o-t —CHy),
CH,0H Hp—O—C—CH,
Glucose §
Glucose pentaacetate
*+5CHsCOOH
ConcentApplied
2 —OH group reacts with acetic anhydride while
aldehyde group does not react with anhydrides
°
il
R-OH+(CH,CO),0—> R—-O—C—CH,
D- qolastese and @-!
auucert and o-b-
#) Ye baie abuselural
tro! sboach “u mode
ccllulexe made
CHO onc
5) om, > roe”
25. (i) (CHOH), > (HOH,
CH,OH CH,OH
Ctucoseeynohyérin
(il) D-Glucose gets oxidised to carboxylic acid (gluconic
acid) on reaction with bromine water.
cro coos
Brvater
IcHOH, ete. aon,
CH40H CH,OH
_-Gicose ucla
(iil) On proionged heating with Hi, D-glucose forms
orhexane.
CHO
| Ha.
{CHOH), “> cH, —(CH,),—CH,
buon pHevane
Dlucose
glucese
Liye.
De
a
ert, Ws Bo ar lle
wae
Pi eu
[Topper’s Answer, 2023]
26. (i)
hexane,
Glucose when heated with red P and HI gives
CHO, EH + CH,CH;CH,CH;CHsCHs
vierane
It indicates the presence of straight chain of six carbon
atoms in glucose.
(i On acetylation with acetic anhydride, glucose gives
a pentaacetate. This confirms that glucose contains
five ~OH groups.
cro
(HOH, +5(CHyCO),0 —>
CH,OH CHO 9
Glucose | I
oH —O~C—CH,)4+ 5CHsCOOH
Glucose pentascetateGlucose 09 oxidation with a mild oxidising agent like
A ie water Bes BUCOMic Acid containing the same
Tarpon atoms 35 present in ghicose. This indicates
A ecence of aldehyde group
cHO coon
8eyH,0
CHOH), +(0) —=""_, (HOM,
CH;OH cHLOH
‘Gluconic acid
+ (a) O-Glucose gets oxidised to carboxylic acid
nic acid) 0n reaction with bromine water.
cHO Goon
water
(HOH, > (CHOW),
ad
cH,OH CH,OH
D.Glucose Gluconic acid
CN
A
CHO. ie Non
py) CHOM. > (CHOH,
i
° Glucose yanobyarin
=) Onacetyiation with acetic anhydride, glucose gives
+ pentaacetate. This confirms that glucose contains
ye OH groups,
cHO
+5(CH;CO),0
ge
(CH—-O—C— CHa), # SCHsCOOH
Cy -O—F— chy
°
‘Glucose pentaacetate
2 (a) Reducing sugar are those carbohydrates which
have free aldehydic or ketonic group i.e., they reduce
Fehling's solution and Tollens’ reagent. e.g., Maltose and
Lactose.
(8) Monosaccharide : Fructose, Galactose
Disaccharides : Sucrose, Lactose
(0 Carbohydrate gets stored in animal body as
slycogen. It is known as animal starch as its structure is
sinilar to amylopectin (ie, starch)
OR
fl) Anomers ie., a-D-glucose and f-D-glucose
fil Presence of aldehyde ie., -CHO group is detected
enreaction of glucose with Br water.
28. (a) Glycosidic linkage.
(b)_ The hydrolysis products of sucrose are u-D-glucose
and B-D-fructose.
305
‘
SINo ‘Amylopectin
1 tis a Iinear It is ahighly branched
condensation polymer polymer in which
of «-D-glucose in which -D-glucose is linked
Cy of one glucose with Cy-C, linkage
Unit is attached to Cy | and C)-C, linkage is
of the other through present hetween two
LBlcosidic linkage linear chains,
Amylose
2. Itis water soluble.
soluble in water.
this
oR
(<) (The sugars which contain free aldehydic or ketonic
Broup and reduce Fehling’s solution and Tollens' reagent
are called reducing sugars,
Ui)” Sucrose is dextrorotatory but after hydrolysis gives
dextrorotatory glucose and laevorotatory fructose.
Since the laevorotation of fructose (-92.4") is more
than dextrorotation of glucose (+52.5°), the mixture is
laevorotatory.
80. (a) Absence of free CHO group.
(b) Vitamin C cannot be stored in our body because
it is a water soluble vitamin and is readily excreted
through urine.
(9) (i) The —CONH— linkage between two amino
acids is called peptide linkage.
Ail) The loss of biological activity of a protein by
Changing the pH, temperature due to disruption of
the native structure of protein is called denaturation,
During denaturation, secondary and tertiary structures
of protein are destroyed but primary structure remains
intact.
OR
(2) i) The pair of stereoisomers which differ only in
the configuration of the hydroxyl group at C, are called
anomers.
(ii) A linkage between two monosaccharides units
through oxygen atom is called glycosidic linkage.
31, (a):The sequence of amino acids in a polypeptide
chain is called primary structure of proteins.
32. (bj:f:pleated sheet structure in proteins refers to
secondary structure.
33. (b):o-Helix is a secondary structure of protein.
34, (d):Curdling of milk is an example of denatured
protein and a-helix represents secondary structure of
protein.
25. (b):Essential amino acids must be taken through diet
as these cannot be synthesised in the body.
36, (b):Helix structure of proteins is stabilised by
hydrogen bonds.
37. (c}:Peptide linkage is present in proteins.| called peptide linkage.
8. (c):Amino acid contains both basic (-NH3} and acidic
group (COOH! hence. there are amphotericin nature,
59. (c)-Albumin is a globular protein, The chains of
polypeptides coil around to give a spherical shape.
40. Peptide linkage is an amide linkage formed between
COOH group of one camino acid and —NH> group
‘of the other amino acid by loss of 3 molecule of water
whereas 2 linkage between two monosaccharides units
through oxygen atom is called glycosidic linkage.
41. (a) The pair of stereoisomers which differ only in
the configuration of the hydroxyl group at C; are called
(b) Essential amino acids : Amino acids which cannot be
synthesized in the body and must be obtained through
diet are known as essential amino acids, eg. valine,
leucine, et.
(©). Denaturation : The loss of biological activity of a
protein by changing the pH, temperature or by adding
some salt due to disruption of the native structure of
protein is called denaturation.
During denaturation. secondary and tertiary structure of
proteins destroyed but primary structure remains intact
42. Characteristic differences between globular and
fibrous proteins can be given 35:
Fibrous pote
“S\No. Globular proteins
1 These arecross- These are linear
linked proteins and condensation
are condensation polymer.
product of acidic and
basic amino acids. a
2 These are soluble in These are insoluble in
water, mineral acids water but soluble in
and bases. strong acids and bases.
A pile A ainde Wwkage is nahonsbe
Femation el prota
(HIDCHsecrmrchensn cy
ny
2 These proteins have These are linear
three dimensional polymers held
folded structure. together by
These are stabilised | intermolecular
by internal bydrogen | hydrogen bonds, ¢;
bonding.es.¢x8 ai silk a
abumin, enzymes
43, Globular protein ~ Insulin
Fibrous protein ~ Keratin
44, As amino acids have both acidic (carboxy!
and basic groups (amino group) in the same mee
they react with both acids and bases. Hence. they 7
amphoteric behaviour.
cng
‘> Amphoteric compounds react oth with acids ang
bases,
Acidic amino acids are those which contain
‘numberof carboxy! groups as compared to amino
Whereas basic amino acids are those which containg
‘more number of amino groups than carboxy! groups,
46, (a) The loss of biological activity of a protein by
changing the pH, temperature due to the disruption gf
the native structure of protein is called denaturation
During denaturation, secondary and tertiary structure
of protein are destroyed but primary structure remains
intact.
{b) An equimolar mixture of glucose and fructose,
obtained by hydrolysis of sucrose in presence of an
acid or the enzyme invertase is called invert sugar, 3s
hydrolysis of sucrose brings about a change in the sign of
rotation, from dextro (+) to laevo (-).
47. Disruption of native conformation of protein by
changing its environment resulting in loss of biological
-xtivity is known as denaturation of protein.
Proteins are very sensitive to the action of heat change
‘of pH. presence of electrolytes and radiation (particulary
short wavelengths).
Whenever proteins are subjected to such changes in the
surroundings, they undergo some structural changes
leading to the disruption of three dimensional structure
Thus, causes permanent loss of activity of proteins
During denaturation, 2° and 3° structures are destroyed
but 1° structure remains intact
The ternalise n= hover on 0
4 glices ubih HI ateuy thet
Paver qhun char etuelity
the.
[Topper's Answer, 2023]
——piomolecules
12 (The loss of biological activity of a protein by
enanging the pH, temperature or by adding some salt due
to disruption of the native structure of protein is called
tenaturation
urine denaturation, secondary and tertiary structure of
proteins destroyed but primary structure remains intact
fe normal shape of protein gets deformed because some
ottydrogen bonds are broken ands referred as denatured
proteins. 8 curing of milk, coagulation of egg white on
paling et
ii) Essential amino acids : Amino acids which cannot be
{inthesizedin the body and must be obtained through diet
St qnown as essential aminoacids, eg, valine, leucine, ee,
= (a). Asaminoacids have bath acidic (carboxyl group)
snd basic groups (amino group) in the same molecule,
they react with both acids and bases. Hence, they show.
amphoteric behaviour.
io) Ince structure, intramolecular H-bonding takes
whereas in pleated structure, intermolecular
Febonding takes place
Cap
2 acHelix is having coiled structure while f-pleated is
rot planar but slightly pleated, eg, froin.
51. (@). The two monosaccharides are joined together
by an oxide linkage formed by the loss of water molecule.
such linkages called elycsii linkage
HOH
HOH
H
OH H
HO
OH
°
HO,
CH,OH
OH H
(b) Primary structure : The specific sequence in which
the various amino acids present in a protein are linked to
‘one another is called its primary structure. Any change in
the primary structure creates a different protein.
(@ Disaccharides are the carbohydrates which on
hydrolysis give two molecules of the same or different
‘monosaccharides. Their general formula is Cy,H7201+
In disaccharides, the two monosaccharides are joined
together by glycosidic linkage.
52. (a) On oxidation with nitric acid, D-glucose yields
saccharic acid.
fo COOH
cone i
(cron STEHNOS, CHOW
|
CH,OH COOH
Dose Dacha aid
307
(b) As amino acids have both acidic (carboxy group)
and basic groups (amino group) in the same molecule,
they react with both acids and bases. Hence, they show
amphoteric behaviour.
(2) Ina-helix structure, intramolecular H-bonding. takes
place whereas in [pleated structure, intermolecular
H-bonding takes place.
53. Proteins are the biomolecules of the living
‘system made up of nitrogenous organic compounds by
condensation polymerisation of «-amino acids.
On the basis of molecular structure, proteins are
classified as
(a) Fibrous proteins : In fibrous proteins, polypeptide
cchains are parallel and are held together by hydrogen and
disulphide bonds. These are insoluble in water, eg.. keratin
and myosin,
(b) Globular proteins : Globular proteins result when the
Polypeptide chains coil around to give three dimensional
‘spherical shape. These are soluble in water, eg., insulin and
albumin
54. (i) Amylose is a linear condensation polymer of
a-D-glucose in which C, of one glucose unit is attached
to Cz of the other through a-glycosidic linkage while
amylopectin is a highly branched polymer in which
o-D-glucose is linked with Cy-C, linkage and Cy-Cy
linkage is present between two linear chains.
(ii)_ Peptide linkage is an amide linkage formed between
—COOH group of one a-amino acid and NH, group
of the other amino acid by loss of a molecule of water
whereas a linkage between two monosaccharides units
through oxygen atom is called glycosidic linkage.
(il) Characteristic differences between globular and
fibrous proteins can be given as
a
S.No. | Globular proteins Fi
1. | These are cross- | These are linear
linked proteins and | condensation
are condensation | polymer.
product of acidic and |
basic amino acids,
These are soluble in These are insoluble in
| water, mineral acids _ water but soluble in
strong acids and bases,
3. | These proteins have These are linear
three dimensional polymers held
folded structure. together by
These are stabilised | intermolecular
by internal hydrogen bonds,eg, |
hydrogen bonding, | hair, silk. |
eg, egg albumin, |
enzymes | |
55. (i) Proteins are the polymers of a-amino acids
linked by amide formation between carboxyl and amino
group. This is called peptide linkage or peptide bond, e3..308
= ° o
—NH—CH—C—NH—CH—C—
| 7]
L kod OR
Peptidelinkoge
(ii) Primary structure : The specific sequence in which
the various amino acids present in a protein are linked te
‘one another is called its primary structure. Any change in
the primary structure creates a different protein.
(ii) Denaturation : The loss of biological activity of a
protein by changing the pH, temperature or by adding
some salt due to disruption of the native structure of
protein is called denaturation.
During denaturation, secondary and tertiary structure of
proteins destroyed but primary structure remains intact.
56. (i) Organic compounds containing both amino
(—NH;) and carboxyl (~COOH) functional groups are
called amino acids.
R-GA—COOH
NH,
(ii) As amino acids have both acidic (carboxyl group)
‘and basic groups (amino group) in the same molecule,
they react with both acids and bases. Hence, they show
amphoteric behaviour
(i) Acidic amino acids are those which contain more
number of carboxyl groups as compared to amino groups
wheress basic amino acids are those which contains
more number of amino groups than carboxyl groups.
(iv) Amino acids which cannot be synthesized in the
body and must be obtained through diet are known as
essential amino acids, eg. valine, leucine, etc
(\) Proteins are the polymers of «-amino acids linked
by amide formation between carboxyl and amino group.
This is called peptide linkage or peptide bond, €3.
i
—NH—CH—C—NH—CH—C—
pecan
R L R
Peptide linkage
57. {c):The chemical name of vitamin Cis ascorbic acid.
58. Vitamin C is soluble in water and regularly excreted
inurine and hence cannot be stored in body.
59. Vitamin D 60. Vitamin C
61. Organic compounds required in the diet in small
amounts to perform specific biological functions for
normal maintenance of optimum growth and health of
the organism are called vitamins.
Vitamins are classified into two groups depending upon
their solubility in water or fat.
(i) Fat soluble vitamins, (eg, vitamin A and D)
(ii) Water soluble vitamins, (eg, vitamin B and C)
62. (a) Maltose #9455 _ Glucose + Glucose
(6) chelix structure of protein stabilised by hydrogen
bonding,
(Vitamin Byz
(IEEE CBSE Champion Chemistry Classy
63. Vitamins are clasifed into two groups depending
upon their solubility in water or fat.
(i) Fat soluble vitamins, (eg. vitamin A and D)
{i)_ Water soluble vitamins, (eg, vitamin B and ¢)
Vitamin K is responsible for the coagulation of blood,
64. (a) Vitamin B, is also called pyridoxit
(b)_ Vitamin K deficiency causes increased blood clotting
time.
(c) Xerophthalmia is caused by the deficiency of vitamin
A. Fish liver oil, carrots, butter and milk etc. are the
source of vitamin A.
OR
(o)_ Vitamin Ciswater soluble vitamin. It mustbe supplied
regularly in diet because they are readily excreted in
urine and cannot be stored in our body. Scurvy (bleeding
‘gums) disease is caused by the deficiency of vitamin C
65. (d):Uracil base is present in RNA.
66, (b):Nucleoside contains pentose sugar and base
whereas nucleotide contains pentose sugar, base as well
as phosphate group.
Nucleoside = Base + Sugar
Nucleotide = Base + Sugar + Phosphate,
67. (d):Thymine is present in DNA but not in RNA,
68. (¢):Nucleic acids are polymer of nucleotides.
69. (¢):Nucleosides are composed of a pentose sugar
and a nitrogenous base.
cmm@
‘2 Nucleotide = Nucleoside + Phosphoric acid
70. A.unit formed by attachment of base to 1” position
of sugar is known as nucleoside.
71. Complete hydrolysis of DNA (or RNA) yields 2
pentose sugar, phosphoric acid and nitrogen containing
heterocyclic compounds as bases.
72. Nucleoside contains pentose sugar, and base
whereas nucleotide contains pentose sugar, base as well
as phosphate group.
Nucleoside = Base + Sugar
Nucleotide = Base + Sugar + Phosphate
qImniG
2 Nucleoside + Phosphate = Nucleotide
73. Phosphodiester linkage
74, (a) On oxidation with nitric acid, D-glucose yields
saccharic acid,
ioe COOH
conctno,
(HoH, SEENON (CHOI,
|
(CH,OH_ ‘COOH
Deas Saccharica
(b) The sugar in DNA is deoxyribose while that in RNA
eeBiomolecules
ig ribose, DNA has a double-stranded helical structure,
while RNA has a single-stranded helical structure.
75, Structural differences between DNA and RNA.
{i)__ The sugar in DNA is deoxyribose while that in RNA
{ij)_ DNA has a double-stranded helical structure, while
RNA has a single-stranded helical structure,
Functional differences between DNA and RNA
{i) DNA is the chemical basis of heredity and is
responsible for maintaining the identity of different
species.
(i) RNAmolecules are responsible for protein synthesis
but the message for the synthesis of a particular protein
ispresent in DNA.
amg
> RNA is having one extra OH in its sugar unit, Also
bases present in RNA are adenine, cytosine, uracil and
guanine, while in DNA these are thyamine, cytosine,
adenine and guanine,
76. (a) As glucose forms a six-membered ring in which
=CHO group combines with ~OH group at C-5, penta-
acetate of glucose does not react with hydroxylamine
due to the absence of free CHO group.
(b) Amino acids behave like salts rather than simple
amines or carboxylic acids. This behaviour is due to the
presence of both acidic (carboxyl group) and basic (amino
groups) group in the same molecule.
(q) Water soluble vitamins must be taken regularly
in diet because they are readily excreted in urine and
cannot be stored (except vitamin B 2) in our body.
(4) The two strands in DNA are complementary to each
other because the hydrogen bonds are formed between
specific pairs of bases. Adenine forms hydrogen bonds
with thymine whereas cytosine forms hydrogen bonds
with guanine.
77. (i) Characteristic differences between globular
and fibrous proteins can be given as:
Fibrous proteins
These are linear
condensation
polymer.
| These are cross-linked
proteins and are
condensation product
of acidic and basic
____ amino acids.
These are insoluble
2. | These are soluble in
water, mineral acids | in water but soluble
and bases, in strong acids and
| bases.
309
These are linear
polymers held
together by
intermolecular
hydrogen bonds. e..
hair, silk
These proteins have
three dimensional
folded structure,
| These are stabilised
| by internal hydrogen
| bonding, eg. e8@
| albumin, enzymes
(il) Amino acids which cannot be synthesized in the
body and must be obtained through diet are known as
essential amino acids, eg., valine, leucine, etc. The amino
acids, which can be synthesised in the body, are known as
non-essential amino acids.
(i) The sugar in DNA is deoxyribose while that in RNA
is ribose. DNA has a double-stranded helical structure,
while RNA has a single-stranded helical structure.
78. (a) Actually, glucose exists in the cyclic hemiacetal
form with only a small amount (< 0.05%) of the open
chain form. Since, the concentration of the open chain
form is low and its reaction with 2,4-DNP is reversible,
therefore, formation of 24-DNP derivative cannot
disturb the equilibrium to regenerate more of the open
chain form from the cyclic hemiacetal form and hence,
does not give this test.
2 99.95% glucose exists in cyclic hemiacetal form.
(b) The two strands in DNA molecule are held together,
by the hydrogen bonds between purine base of one
strand and pyrimidine base of the other and vice versa.
Because of different sizes and geometries of the bases,
the only possible pairing in DNA are G (guanine) and C
(cytosine) through three H-bonds, ie, (C=G) andbetween
A(adenine) and T (thymine) through two H-bonds (ie, A= 1).
Due to this base-pairing principle, the sequence of
bases in one strand automatically fixes the sequence
of bases in the other strand. Thus, the two strands are
complementary and not identical.
(c)_ The basic structural difference between starch and
cellulose is of linkage between the glucose units. In starch,
there is a-D-glycosidic linkage. Both the components of
starch-amylose and amylopectin are polymers of «-D-
glucose. On the other hand, cellulose is a linear polymer of
8-D-glucose in which C1 of one glucose unit is connected to
C4 of the other through [}-D-glycosidic linkage.
79. (i)
Amylose ‘Amylopectin |
15-20% part of | 80-85% part of starch
starch, |310
2. | Made up of linear
chain polymers of
a-D glucose with
LL C1-C4 linkage.
| 3. Water soluble
Made up of branched
polymers of -D glucose
with C1-C4 and C1-C6
linkage between two chains |
Water insoluble
(ii) Characteristic differences between globular and
fibrous proteins can be given as :
_S.No. Globular proteins _
1. | These are cross-
linked proteins and _| condensation
| are condensation polymer. |
| product of acidic and |
basic amino acids. _ |
2. | These are soluble in | These are insoluble in |
water, mineral acids | water but solublein |
___ and bases. | strong acids and bases. |
3. "| These proteins have These are linear
| three dimensional polymers held
folded structure. together by |
These are stabilised | intermolecular |
| by internal hydrogen | hydrogen bonds,eg., |
| bonding, e.g., €88 hair, silk. |
albumin, enzymes. |
(iii) Nucleoside contains pentose sugar, and base
whereas nucleotide contains pentose sugar, base as well
as phosphate group.
Nucleoside = Base + Sugar
Nucleotide = Base + Sugar + Phosphate
__ Fibrous proteins ‘|
These are linear
80. (a) An equimolar mixture of glucose and fructose,
obtained by hydrolysis of sucrose in presence of an acid
or the enzyme invertase is called invert sugar.
(b) Native protein : Protein purified from natural source
which includes blood, plasma from animal etc.
(c) When nucleoside is linked to phosphoric acid at
5’-position of sugar moiety, we get a nucleotide.
~ a
CBSE Sample Questions
CBSE Ch
CHO COOH
| 7
(HOH, HHNOs . (CHOH),
CH,OH
Glucose
COOH
Saccharic a
(B)
5. (a) The —OH group prese
glucose molecule forms a six-
—CHO group to form a cyclic hy
glucose does not give a positi
reagent in the Schiff’s test.
(b) The carbonyl group prese
6. (a) Acetylation of glucc
gives glucose pentaacetate w!
of five —OH groups. Since, it €
five —OH groups should be a
atoms
CHO
(CHOH), Acetic Anhydride
CH,OH
(b) Glucose reduces Fehlin
H oO
NF
i
H-C-—OH
HO-CH acu + 2,0
eee
H-C-OH
|
CH,OH
(a) CHO
1,