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.
Key concepts
Hover a concept to preview it and jump to its most relevant Q&A.
Carbohydrates
Carbohydrates are organic compounds built from carbon, hydrogen and oxygen in a ratio close to (CH2O)n, which is why they are also called saccharides.
Most relevant Q&A
- Give IUPAC names to the following monosaccharides. 1. $CHO-CHOH-CH_2OH$ 2. $CHO-(CHOH)_3-CH_2OH$ 3. $CH_2OH-CO-(CHOH)_3-CH_2OH$Preview
- • Is galactose an aldohexose or a ketohexose? • Which carbon in galactose has different configuration compared to glucose? • Draw Haworth fo…Preview
- The disaccharide sucrose gives negative Tollens test while the disaccharide maltose gives positive Tollens test.Free
- Make models corresponding to the two Haworth formulae of sucrose in Fig. 14.8. Check that both are identical. ![Maharashtra Board Class 12 C…Preview
- • What are the constituents of balanced diet ? • What are the products of digestion of carbohydrates? • Which constituent of diet is useful…Preview
In previous exams
How often this chapter’s concepts have been examined — real appearance data, never estimated.
Chapter contents
The NCERT structure, section by section. Open a section to see its questions, then read the concept-first solution.
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.
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.
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…
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…
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…
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…
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.
Structure and properties of glucose
2 QGlucose'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…
+−Can you recall?i1 question
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).
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…
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…
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…
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…
Sucrose
Sucrose, C12H22O11, is the most common disaccharide of everyday life (ordinary table sugar) and is strongly dextrorotatory, with specific rotation +66.5 degrees.
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.
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…
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…
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…
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…
+−Can you think? 14.2.101 question
Glycogen
Glycogen is the carbohydrate reserve that animals store, functionally the direct animal-kingdom counterpart of plant starch.
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…
α-Amino acids
3 QComplete 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.
+−Use your brain poweri1 question
+−Can you think? 14.3.11 question
+−Can you recall?i1 question
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.
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…
Globular proteins
Globular proteins are proteins whose individual polypeptide-chain molecules adopt an overall compact, roughly SPHERICAL shape.
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.
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…
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…
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…
Tertiary structure of proteins
2 QThe 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…
+−Use your brain poweri1 question
+−Can you tell? 14.3.41 question
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,…
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,…
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…
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…
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.
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…
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…
1. Select the most correct choice.
The end-of-chapter questions of this group, exactly as the book prints them.
+−Select the most correct choice6 questions
- Q1CH2OH-CO-(CHOH)4-CH2OH is an example of a. Aldohexose b. Aldoheptose c. Ketotetrose d. KetoheptoseFree
- Q2Open chain formula of glucose does not contain a. Formyl group b. Anomeric hydroxyl group c. Primary hydroxyl group d. Secondary hydroxyl gr…Free
- Q3Which of the following does not apply to CH2NH2 - COOH a. Neutral amino acid b. L - amino acid c. Exists as zwitter ion d. Natural amino aci…Preview
- Q4Tryptophan is called essential amino acid because a. It contains aromatic nucleus. b. It is present in all the human proteins. c. It cannot…Preview
- Q5A disulfide link gives rise to the following structure of protein. a. Primary b. Secondary c. Tertiary d. QuaternaryPreview
- Q6RNA has a. A - U base pairing b. P-S-P-S backbone c. double helix d. G - C base pairingPreview
2. Give scientific reasons :
The end-of-chapter questions of this group, exactly as the book prints them.
+−Give scientific reasons5 questions
- Q1The disaccharide sucrose gives negative Tollens test while the disaccharide maltose gives positive Tollens test.Free
- Q2On complete hydrolysis DNA gives equimolar quantities of adenine and thymine.Free
- Q3α - Amino acids have high melting points compared to the corresponding amines or carboxylic acids of comparable molecular mass.Preview
- Q4Hydrolysis of sucrose is called inversion.Preview
- Q5On boiling egg albumin becomes opaque white.Preview
3. Answer the following
The end-of-chapter questions of this group, exactly as the book prints them.
+−Answer the following4 questions
- Q1Some of the following statements apply to DNA only, some to RNA only and some to both. Label them accordingly. a. The polynucleotide is doub…Free
- Q2Write the sequence of the complementary strand for the following segments of a DNA molecule. a. 5' - CGTTTAAG - 3' b. 5' - CCGGTTAATACGGC -…Free
- Q3Write the names and schematic representations of all the possible dipeptides formed from alanine, glycine and tyrosine.Preview
- Q4Give two evidences for presence of formyl group in glucose.Preview
4. Draw a neat diagram for the following:
The end-of-chapter questions of this group, exactly as the book prints them.
Activity :
The end-of-chapter questions of this group, exactly as the book prints them.
Sample & Board Papers
Sample papers and previous-year board questions for this subject.
+−Show 30 questionsHide questions30 questions
- Q1Define antioxidants. Draw structure of BHT.Preview
- Q2What are carbohydrates? Write the reaction for the preparation of nylon-6.Preview
- Q3Which of the following is NOT present in DNA? (a) Adenine (b) Guanine (c) Thymine (d) UracilPreview
- Q4Phenelzine is used as an _______. (a) analgesic (b) antiseptic (c) antipyretic (d) antidepressantPreview
- Q5Which of the following vitamins is the vitamin of alicyclic series? (a) Vitamin C (b) Vitamin K (c) Vitamin B (d) Vitamin APreview
- Q6Explain the preparation of glucose from cane sugar.Preview
- Q7What are 'nucleic acids'? Define complex lipids. Mention any 'two' functions of lipids.Preview
- Q8The number of primary and secondary hydroxyl groups in ribose are — (a) 1, 3 (b) 2, 3 (c) 3, 1 (d) 3, 2Preview
- Q9What are amino acids? Write the correct reaction for formation of peptide bond between amino acids.Preview
- Q10How glucose is prepared from cane sugar? Write the formula of the complex copper (II) hexacyano ferrate (II).Preview
- Q11Write the molecular formula of novestrol.Preview
- Q12Write the number of hydroxyl groups present in α–D–(+)–Glucopyranose (trans).Preview
- Q13What are antacids? Write the main constituents of dettol.Preview
- Q14How is glucose prepared by commercial method? How is peptide linkage formed?Preview
- Q15Name the reagent which on reaction with glucose confirms the presence of five hydroxyl groups in glucose: (a) Hydroxyl amine (b) Bromine wat…Preview
- Q16Identify antibiotic drug amongst the following: (a) Codeine (b) Equanil (c) Penicillin (d) ValiumPreview
- Q17Define optical activity. How many optical isomers are possible for glucose?Preview
- Q18Write Howorth projection formula of $\alpha$-D-(+)-glucopyranose. Define hormones.Preview
- Q19What are monosaccharides? Explain denaturation of proteins.Preview
- Q20What are soaps? How are soaps prepared? Define antiseptic.Preview
- Q21Explain formation of peptide linkage in protein with an example.Preview
- Q22Write commercial method for preparation of glucose. Write structure of adipic acid.Preview
- Q23The glycosidic linkage present in maltose is _______. (a) $\alpha,\beta$-1,2-glycosidic linkage (b) $\alpha$-1,4-glycosidic linkage (c) $\be…Preview
- Q24Write chemical reaction for the preparation of glucose from sucrose. Write structure of D-ribose.Preview
- 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
- Q26Write classification of proteins with an example.Preview
- Q27Write preparation of glucose from sucrose.Preview
- Q28What is peptide bond? How is it formed? Write the name and formula of the reagent used to convert alkylhalide to nitroalkane.Preview
- Q29(a) Write the reaction of bromine water on glucose. (b) Define – EnantiomersPreview
- Q30(i) What is peptide linkage? (ii) Write general characteristics of interhalogen compounds.Preview