Xii Chem Q and A CH 14
Xii Chem Q and A CH 14
BIOMOLECULES
(QUESTIONS & ANSWERS)
14.1 Glucose or sucrose are soluble in water but cyclohexane or benzene (simple six membered ring compounds)
are insoluble in water. Explain.
Ans. Glucose and sucrose molecules contain many – OH groups and hence are capable of forming H-bonds with
water molecules. On the other hand cyclohexane and benzene are hydrocarbons and hence cannot form H-
bonds with water. Therefore, glucose and sucrose are soluble in water whereas cyclohexane and benzene are
not soluble in water.
14.3 How do you explain the absence of aldehyde group in the pentaacetate of D-glucose?
Ans. Since pentaacetate of glucose are not oxidised by Tollen's reagent or Fehling's solution indicating the absence
of D-glucose.
14.4 The melting points and solubility in water of amino acids are generally higher than that of the corresponding halo
acids. Explain.
Ans. The amino acids exists as a zwitterions.
H3N+ – CHR – COO–
Due to this dipolar salt like character they have strong dipole attractions or electrostatic attractions. Therefore,
their melting points are higher than that of corresponding halo acids.
Due to salt like character of amino acids their solubility is higher than the corresponding halo acids.
14.5 Where does the water present in the egg go after boiling the egg?
Ans. When the egg is boiled, the proteins first undergo denaturation and then coagulation and the water present in
the egg get absorbed.
14.7 What products would be formed when a nucleotide from DNA containing thymine is hydrolysed?
Ans. Besides thymine, the two other products are-2 deoxy-D-ribose and phosphoric acid.
14.4 Classify the following into monosaccharides and disaccharides. Ribose, 2-deoxyribose. maltose, galactose,
fructose and lactose.
Ans. Monosaccharides - Fructose, Galactose, Ribose and 2-deoxyribose
Disaccharides - Maltose, Luctose.
14.7 What are the hydrolysis products of (a) sucrose and (b) lactose ?
Ans. Hydrolysis products of sucrose - Glucose, Fructose
Hydrolysis products of lactose - Glucose, Galactose.
STUDY MATERIAL: XII CHEMISTRY 2 BIOMOLECULES (Q & A)
14.8 What is the basic structural difference between starch and cellulose ?
Ans. Starch is a polymer of -glucose. It consists of a linear polymer of -gulcose (called amylose) and a branched
- chain polymer of -glucose.
14.9 What happens when D-glucose is treated with the following reagents?
(i) HI (ii) Bromine water (iii) HNO3
CHO
|
Ans. (i) (CHOH)4 + HI –––––CH3 – CH2 – CH2 – CH2 – CH2 – CH3
|
CH 2OH
D-Glucose
14.10 Enumerate the reactions of D-glucose which cannot be explained by its open chain structure.
Ans. (1) Aldehydes give 2, 4-DNP test, Schiff's test, and react with NaHSO4 to form the hydrogen sulphite addi-
tion product. However, glucose does not undergo these reactions.
(2) The pentaacetate of glucose does not react with hydroxylamine. This indicates that a free – CHO group is
absent from glucose.
(3) Glucose exists in two crystalline forms – and . The -form (m.p. = 419 K) crystallises from a concen-
trated solution of glucose at 303 K and the -form (m.p = 423 K) crystallises from a hot and saturated
aqueous solution at 371 K. This behaviour cannot be explained by the open chain structure of glucose.
14.11 What are essential and non-essential amino acids? Give two examples of each type.
Ans. Essential amino acids are required by the human body, but they cannot be synthesised in the body. They must
be taken through food. For example: valine and leucine Non-essential amino acids are also required by the
human body, but they can be synthesised in the body. For example: glycine, and alanine
14.19 How are vitamins classified? Name the vitamin responsible for the coagulation of blood.
Ans. On the basis of their solubility in water or fat, vitamins are classified into two groups.
(i) Fat-soluble vitamins: Vitamins that are soluble in fat and oils, but not in water, belong to this group.
For example: Vitamins A, D, E, and K
(ii) Water-soluble vitamins: Vitamins that are soluble in water belong to this group.
For example: B group vitamins (B1, B2, B6, B12, etc.) and vitamin C However, biotin or vitamin H is
neither soluble in water nor in fat. Vitamin K is responsible for the coagulation of blood.
14.20 Why are vitamin A and vitamin C essential to us? Give their important sources.
Ans. The deficiency of vitamin A leads to xerophthalmia (hardening of the cornea of the eye) and night blindness. The
deficiency of vitamin C leads to scurvy (bleeding gums). The sources of vitamin A are fish liver oil, carrots,
butter, and milk. The sources of vitamin C are citrus fruits, amla, and green leafy vegetables.
14.23 The two strands in DNA are not identical but are complementary. Explain.
Ans. In the helical structure of DNA, the two strands are held together by hydrogen bonds between specific pairs of
bases. Cytosine forms hydrogen bond with guanine, while adenine forms hydrogen bond with thymine. As a
result, the two strands are complementary to each other.
14.24 Write the important structural and functional differences between DNA and RNA.
––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––
Ans. DNA RNA
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1. The sugar present in DNA is 1. The sugar present in RNA is
2-deoxy-D-(–)-ribose. D-(–) - ribose.
2. DNA has double stranded -helix structure. 2. RNA has single stranded -helix structure.
3. DNA contains cytosine and thymine as 3. RNA contains cytosine and uracil as
pyrimidine bases. pyrimidine bases.
4. DNA has unique property to replicate. 4. RNA usually not replicate.
5. DNA are responsible for heredity character. 5. RNA controls protein synthesis.
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14.25 What are the different types of RNA found in the cell?
Ans. (i) Messenger RNA (m-RNA) (ii) Ribosomal RNA (r-RNA) (iii) Transfer RNA (t-RNA)
Q.22 Write down the structures and names of products formed when D-glucose is treated with;
(a) (i) Hydroxylamine (ii) HI (iii) Ammonical silver nitrate solution.
(b) How are harmones and vitamins different in respect of their sources and functions?
Q.23 (a) State the constitutional difference between DNA and RNA Write down the names of the bases produced
on hydrolysis of DNA.
(b) Draw simple Fischer projections of D-glucose and L-glucose. Can these be called enantiomers?
Q.24 State differences between the following pairs :
(i) -helix and -pleated structures.
(ii) Primary and secondary structures of a protein.
Q.1 Except for vitamin Bl2, all other vitamins of group B; should be supplied regularly in diet. Why ?
Q.2 Write two main functions of carbohydrates in plants.
Q.3 B-Complex is an often prescribed vitamins. What is complex about it and what is its usefulness?
Q.4 Give one example each for reducing and non-reducing sugars.
Q.5 Why are carbohydrates generally optically active ?
Q.6 Name the two components of starch. How do they differ from each other structurally?
Q.7 Name the four bases present in DNA. Which one of the these is not present in RNA?
Q.8 Name two fat soluble vitamins, their sources and the diseases caused due to their deficiency in diet.
Q.9 Name two water soluble vitamins, their sources and the diseases caused due to their deficiency in diet.
Q.10 What are essential and non-essential amino acids? Give one example of each type.
Q.11 Mention the type of linkages responsible for the formation of the following:
(i) Primary structure of proteins. (ii) Cross linking of polypeptide chains.
(iii) -helix formation. (iv) -sheet structure.
Q.12 Write the major classes in which the carbohydrates are divided depending upon whether these undergo hydrolysis,
and if so, on the number of products formed.
Q.13 Name the chemical components which constitute nucleotides. Write any two functions of nucleotides in a cell.
Q.14 An optically active compound having molecular formula C6H12O6 is found in two isomeric forms (A) and (B)
in nature. When (A) and (B) are dissolved in water they show the following equilibrium:
(A) Equilibrium (B)
mixture 19.2°
[ ]D= 111°
52.2°
(i) What are such isomers called? (ii) Can they be called enantiomers? Justify your answer.
(iii) Draw the cyclic structure of isomer (A).
Q.15 Despite having an aldehyde group:
(a) Glucose does not give 2, 4-DNP test. What does this indicate?
(b) Draw the Haworth structure of -D-(+)-Glucopyranose.
(c) What is the significance of D and (+) here?