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Chemistry · Class 12 Science

Ch 14Biomolecules — Class 12 Chemistry, concept-first.

Living organisms are built from a small number of large, repeating classes of molecules, and this chapter studies three of the most important: carbohydrates, proteins and nucleic acids.

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14.1

Introduction: Principal molecules of the living world

Living organisms are built from a small number of large, repeating classes of molecules, and this chapter studies three of the most important: carbohydrates, proteins and nucleic acids.

14.2

Carbohydrates

Carbohydrates are defined chemically, not just by taste: they are polyhydroxy aldehydes or ketones, or compounds that yield such polyhydroxy carbonyl units on hydrolysis.

14.2.1

Classification of carbohydrates

Carbohydrates fall into three broad groups according to how they behave on hydrolysis. Monosaccharides do not hydrolyse into any smaller carbohydrate units at all -- they ARE the smallest unit (exampl…

14.2.2

Nomenclature of monosaccharides

The IUPAC system gives every monosaccharide a systematic name built from two pieces of information: whether its single carbonyl group is an aldehyde or a ketone, and how many carbon atoms the molecule…

14.2.3

Glucose

Glucose is one of the most abundant and important monosaccharides, occurring in nature both in its free form (as in fruit and honey) and combined into larger carbohydrates such as sucrose, starch and…

14.2.3a

Preparation of glucose from sucrose

Sucrose is hydrolysed by warming it with dilute hydrochloric acid or dilute sulfuric acid for about two hours; this splits its single glycosidic linkage and converts the sucrose completely into an equ…

14.2.3b

Preparation of glucose from starch

On a commercial scale, glucose is manufactured by hydrolysing starch rather than sucrose, because starch (from grains such as maize) is a cheaper and more abundant raw material.

14.2.4

Structure and properties of glucose

2 Q

Glucose's open-chain structure -- an aldohexose, CHO-(CHOH)4-CH2OH, with one aldehydic carbonyl at C-1 and a hydroxyl group on each of the other five carbons -- was worked out entirely from chemical e…

14.2.5

Optical isomerism in glucose

Glucose's structural formula, CHO-(CHOH)4-CH2OH, contains four chiral (stereogenic) carbons -- C-2, C-3, C-4 and C-5, each bonded to four different groups (C-1 and C-6 are not chiral).

14.2.6

Ring structure of glucose

The open-chain Fischer structure of glucose, though it correctly explains many of glucose's properties, cannot account for every chemical property glucose is observed to show -- most notably, glucose…

14.2.7

Reducing nature of glucose

The cyclic hemiacetal group present in glucopyranose is not a permanently 'closed' structure -- it sits in a fast equilibrium with a small, ever-present amount of the open-chain form carrying a genuin…

14.2.8

Representation of Fructose structure

Fructose (C6H12O6) is the second monosaccharide studied in detail in this chapter -- a laevorotatory ketohexose, with specific rotation [alpha]D20 = -92.4 degrees; this strong laevorotation is why fru…

14.2.9

Disaccharides

Disaccharides are the most familiar class of oligosaccharide: on hydrolysis with either dilute acid or a specific enzyme, each disaccharide molecule splits into exactly two monosaccharide units, which…

14.2.9a

Sucrose

Sucrose, C12H22O11, is the most common disaccharide of everyday life (ordinary table sugar) and is strongly dextrorotatory, with specific rotation +66.5 degrees.

14.2.9b

Maltose

Maltose, C12H22O11, is a disaccharide built from two units of D-glucose, joined by a glycosidic linkage that runs from C-1 of one glucose ring to C-4 of the other.

14.2.9c

Lactose

Lactose, C12H22O11, is the disaccharide naturally present in milk (both human and animal), and is built from one unit of D-galactose and one unit of D-glucose -- two DIFFERENT monosaccharides, unlike…

14.2.10

Polysaccharides

Polysaccharides are the third and largest class of carbohydrate defined in section 14.2.1: they form when a very large number of monosaccharide units -- hundreds to many thousands -- are linked togeth…

14.2.10a

Starch

Starch, the plant storage polysaccharide, is itself a polymer built entirely of alpha-D-glucose units, but it is not a single uniform substance -- it is a mixture of two distinct components with diffe…

14.2.10b

Cellulose

Cellulose, the principal structural polysaccharide of plants, is -- like amylose -- an unbranched, straight-chain polysaccharide, but built from beta-glucose units (rather than starch's alpha-glucose…

14.2.10c

Glycogen

Glycogen is the carbohydrate reserve that animals store, functionally the direct animal-kingdom counterpart of plant starch.

14.3

Proteins

Proteins are the fundamental structural materials of animal bodies -- they build muscle, skin, hair, nails and connective tissue -- and, in the specialised form of enzymes, they also drive essentially…

14.3.1

α-Amino acids

3 Q

Complete hydrolysis of any protein breaks every peptide linkage in it and yields a mixture of free alpha-amino acids -- the monomer units from which every protein is built.

14.3.2

Peptide bond and protein

The chemical bond that links one alpha-amino acid to the next, building up the polymer chain of a protein, is called the peptide bond.

14.3.3

Types of proteins

Beyond their chemical composition (the sequence of amino-acid residues, discussed from section 14.3.4a onward), proteins can also be classified more simply by the overall molecular SHAPE their polypep…

14.3.3a

Globular proteins

Globular proteins are proteins whose individual polypeptide-chain molecules adopt an overall compact, roughly SPHERICAL shape.

14.3.3b

Fibrous proteins

Fibrous proteins are proteins whose individual polypeptide-chain molecules adopt an overall elongated, ROD-like shape, rather than the compact sphere of a globular protein.

14.3.4

Structure of proteins

Beyond simple shape classification (globular vs fibrous, section 14.3.3), the true diversity of protein shapes and functions -- from the load-bearing fibres of hair and muscle, to the catalytic pocket…

14.3.4a

Primary structure of proteins

The primary structure of a protein is, most simply, the exact SEQUENCE in which its constituent alpha-amino-acid residues are strung together, one after another, joined by peptide bonds -- it is the m…

14.3.4b

Secondary structure of proteins

The secondary structure of a protein describes the regular, LOCAL three-dimensional shape that a stretch of the polypeptide backbone folds into, distinct from (and nested within) the larger overall te…

14.3.4c

Tertiary structure of proteins

2 Q

The tertiary structure of a protein is the overall, non-repeating three-dimensional shape adopted by one ENTIRE polypeptide chain -- the result of the whole chain folding up in a specific way that bot…

14.3.4d

Quaternary structure of proteins

The quaternary structure of a protein is the highest of the four structural levels, and applies only to proteins built from MORE than one separately-folded polypeptide chain: when two or more chains,…

14.3.5

Denaturation of proteins

Denaturation is the process by which a protein's carefully folded, specific three-dimensional shape is disrupted and destroyed by an external physical or chemical stress -- commonly high temperature,…

14.3.6

Enzymes

Enzymes are the biological catalysts responsible for the enormous number of chemical reactions that must occur inside a living body, all proceeding efficiently under the comparatively mild, constant c…

14.4

Nucleic acids

Nucleic acids are the third and final class of biomolecule studied in this chapter, and are distinguished from carbohydrates and proteins by their unique biological role: they are the molecules respon…

14.4.1

Nucleotides

Nucleic acids -- both DNA and RNA -- are unbranched polymers built from repeating monomer units called nucleotides; because of this, nucleic acids are said to have a polynucleotide structure.

14.4.2

Structure of nucleic acids

Both DNA and RNA are true polymers of their nucleotide monomer units, built by repeatedly joining the free 3'-OH group on one nucleotide's sugar to the free 5'-phosphate group of the NEXT nucleotide i…

14.4.3

DNA double helix

In 1953, the scientists James Watson and Francis Crick proposed a now-famous double-helix model for the overall three-dimensional structure of DNA, a model later confirmed directly by electron-microsc…

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3. Answer the following

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Activity :

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Sample & Board Papers

Sample papers and previous-year board questions for this subject.

+Show 30 questions30 questions
  1. Q1Define antioxidants. Draw structure of BHT.Preview
  2. Q2What are carbohydrates? Write the reaction for the preparation of nylon-6.Preview
  3. Q3Which of the following is NOT present in DNA? (a) Adenine (b) Guanine (c) Thymine (d) UracilPreview
  4. Q4Phenelzine is used as an _______. (a) analgesic (b) antiseptic (c) antipyretic (d) antidepressantPreview
  5. Q5Which of the following vitamins is the vitamin of alicyclic series? (a) Vitamin C (b) Vitamin K (c) Vitamin B (d) Vitamin APreview
  6. Q6Explain the preparation of glucose from cane sugar.Preview
  7. Q7What are 'nucleic acids'? Define complex lipids. Mention any 'two' functions of lipids.Preview
  8. Q8The number of primary and secondary hydroxyl groups in ribose are — (a) 1, 3 (b) 2, 3 (c) 3, 1 (d) 3, 2Preview
  9. Q9What are amino acids? Write the correct reaction for formation of peptide bond between amino acids.Preview
  10. Q10How glucose is prepared from cane sugar? Write the formula of the complex copper (II) hexacyano ferrate (II).Preview
  11. Q11Write the molecular formula of novestrol.Preview
  12. Q12Write the number of hydroxyl groups present in α–D–(+)–Glucopyranose (trans).Preview
  13. Q13What are antacids? Write the main constituents of dettol.Preview
  14. Q14How is glucose prepared by commercial method? How is peptide linkage formed?Preview
  15. Q15Name the reagent which on reaction with glucose confirms the presence of five hydroxyl groups in glucose: (a) Hydroxyl amine (b) Bromine wat…Preview
  16. Q16Identify antibiotic drug amongst the following: (a) Codeine (b) Equanil (c) Penicillin (d) ValiumPreview
  17. Q17Define optical activity. How many optical isomers are possible for glucose?Preview
  18. Q18Write Howorth projection formula of $\alpha$-D-(+)-glucopyranose. Define hormones.Preview
  19. Q19What are monosaccharides? Explain denaturation of proteins.Preview
  20. Q20What are soaps? How are soaps prepared? Define antiseptic.Preview
  21. Q21Explain formation of peptide linkage in protein with an example.Preview
  22. Q22Write commercial method for preparation of glucose. Write structure of adipic acid.Preview
  23. Q23The glycosidic linkage present in maltose is _______. (a) $\alpha,\beta$-1,2-glycosidic linkage (b) $\alpha$-1,4-glycosidic linkage (c) $\be…Preview
  24. Q24Write chemical reaction for the preparation of glucose from sucrose. Write structure of D-ribose.Preview
  25. Q25The linkage present in Lactose is _____. (a) α, β -1, 2 - glycosidic linkage (b) α -1, 4 - glycosidic linkage (c) β -1, 4 - glycosidic linka…Preview
  26. Q26Write classification of proteins with an example.Preview
  27. Q27Write preparation of glucose from sucrose.Preview
  28. Q28What is peptide bond? How is it formed? Write the name and formula of the reagent used to convert alkylhalide to nitroalkane.Preview
  29. Q29(a) Write the reaction of bromine water on glucose. (b) Define – EnantiomersPreview
  30. Q30(i) What is peptide linkage? (ii) Write general characteristics of interhalogen compounds.Preview