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NCERT SOLUTIONS FOR CLASS 1 TO 12

Chapter 10 – Biomolecules

Explore NCERT Solutions for Class 12 Chemistry Chapter 10 Biomolecules with solved NCERT exercises, key concepts, important questions, and downloadable PDF for board exams.

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NCERT Solutions for Class 12 Chemistry Chapter 10 – Biomolecules

Chapter 10 of Class 12 Chemistry bridges the world of chemistry and biology in the most profound way. Biomolecules are the chemical compounds that form the basis of all living organisms — from the glucose that powers your cells to the DNA that carries your genetic information. Studying this chapter means studying the very molecules of life, which makes it both intellectually fascinating and directly relevant to both Chemistry and Biology examinations. For Subject Wise NCERT Solutions for class 12 and Chapter-wise NCERT solutions for class 12 Chemistry, check out these pages. 

These NCERT Solutions for Class 12 Chemistry offer clear, comprehensive answers to all exercises in this chapter. The NCERT Solutions Class 12 Chemistry Chapter 10 material provided here explains complex biological terminology in simple chemical language, helping students understand the molecular basis of life and confidently attempt both factual and application-based questions in their examinations.

Find the PDF of All the Exercises of NCERT Class 12 Chemistry Chapter 10 Solutions

All exercise solutions for Biomolecules are available as downloadable PDFs, covering every textbook question on carbohydrates, proteins, lipids, nucleic acids, vitamins, enzymes, and hormones. These PDFs are particularly valuable for NEET aspirants, as the chapter content overlaps with biology, and having chemistry-specific explanations alongside structural details makes revision both thorough and efficient. Students can bookmark key sections for targeted last-minute review before examinations.

For CBSE Class 12 board examinations, this chapter is a consistent source of questions on the classification of carbohydrates, the structure of proteins and their levels of organisation, the role of vitamins and hormones, and the structure and function of nucleic acids. For NEET aspirants in particular, this chapter overlaps significantly with Class 12 Biology content, making it a high-return investment of study time. JEE candidates also encounter questions on the chemistry of amino acids, glucose anomers, and enzyme action.

Important Topics Covered in NCERT Class 12 Chemistry Chapter 10

Carbohydrates: Classification into monosaccharides, disaccharides, and polysaccharides. Important examples: glucose, fructose, sucrose, maltose, lactose, starch, cellulose, and glycogen. Open-chain and cyclic (Haworth) structures of glucose. Anomers (α and β), mutarotation, and the concept of reducing and non-reducing sugars.

Proteins: Amino acids and their classification; peptide bond formation; primary, secondary, tertiary, and quaternary structures of proteins; denaturation of proteins; examples of fibrous and globular proteins.

Enzymes: Nature, properties, and mechanism of enzyme action; the lock-and-key model; enzyme specificity; factors affecting enzyme activity.

Vitamins: Classification into fat-soluble (A, D, E, K) and water-soluble (B complex, C) vitamins; deficiency diseases caused by each vitamin.

Nucleic Acids: Components of nucleotides (nitrogenous bases, pentose sugar, phosphoric acid); structure of DNA (double helix) and RNA (single strand); types of RNA; base pairing rules (Chargaff's rules); role in protein synthesis.

Hormones: Basic classification and functions of important hormones like insulin, adrenaline, and thyroxine; their chemical nature (protein-based or steroid-based).

Lipids: Structure and classification of fats and oils; difference between saturated and unsaturated fats; biological role of lipids in cell membranes and energy storage.

Important Formulas and Key Points of Chapter 10

Concept / Formula

Explanation / Application

Molecular formula of glucose: C₆H₁₂O₆

Glucose is a hexose monosaccharide; same molecular formula as fructose (structural isomers)

Sucrose = Glucose + Fructose (glycosidic bond)

Non-reducing disaccharide; glycosidic bond between C1 of glucose and C2 of fructose; no free anomeric –OH group

Maltose = Glucose + Glucose (α-1,4 glycosidic bond)

Reducing disaccharide; formed during digestion of starch; one free anomeric –OH

Lactose = Glucose + Galactose (β-1,4 glycosidic bond)

Reducing disaccharide; found in milk; lactase enzyme required for its digestion

Peptide Bond: –CO–NH– (formed between –COOH and –NH₂)

Condensation reaction between carboxyl of one amino acid and amino group of another, releasing water

Chargaff's Rule: [A] = [T], [G] = [C]

In DNA, adenine pairs with thymine (2 H-bonds), guanine pairs with cytosine (3 H-bonds)

DNA Sugar: Deoxyribose (lacks –OH at C2); RNA Sugar: Ribose (has –OH at C2)

Structural difference between DNA and RNA at the sugar component

α-glucose: –OH at C1 is on the same side as C6; β-glucose: –OH at C1 is on opposite side

Anomers of glucose; α and β differ at the anomeric carbon (C1); mutarotation interconverts them in solution

Denaturation of Protein

Loss of 3D structure (secondary/tertiary/quaternary) due to heat, pH change, or chemicals; primary structure intact; activity lost

Lock-and-Key Model (Fischer)

Enzyme (lock) has an active site that specifically fits the substrate (key); reaction occurs and product released

Iodine Test for Starch

Starch gives blue-black colour with iodine solution; used to identify starch; glycogen gives reddish-brown colour

Fat-Soluble Vitamins: A, D, E, K

Stored in liver and fatty tissues; excess can accumulate and cause toxicity

Water-Soluble Vitamins: B complex, C

Not stored; excreted in urine; must be supplied regularly through diet

Saponification: Fat + NaOH → Glycerol + Soap (sodium salt of fatty acid)

Hydrolysis of ester bonds in triglycerides under alkaline conditions; basis of soap making

Zwitter Ion (Amphoteric nature of amino acids): ⁺NH₃–CHR–COO⁻

At isoelectric point, amino acid exists as internal salt (zwitter ion); net charge is zero

Key Points, Exam Tips & Common Mistakes

  • Carbohydrates are classified as reducing sugars (have a free anomeric –OH, e.g. glucose, maltose, lactose) or non-reducing sugars (no free anomeric –OH, e.g. sucrose) — this distinction is a very common exam question.

  • Sucrose is the only common non-reducing disaccharide because both anomeric carbons of glucose and fructose are involved in the glycosidic bond, leaving no free –OH to reduce Tollens' or Fehling's reagent.

  • Mutarotation is the spontaneous interconversion of α and β anomers of glucose in aqueous solution; the optical rotation gradually reaches an equilibrium value.

  • The four levels of protein structure — primary (sequence), secondary (α-helix/β-sheet), tertiary (3D folding), quaternary (multiple subunits) — are almost always tested in board examinations.

  • Essential amino acids are those that cannot be synthesised by the body and must be obtained from diet. Glycine is the simplest amino acid and the only one that is not optically active (no chiral centre).

  • Chargaff's base pairing rule (A=T, G≡C) is the molecular explanation for the complementary nature of the two DNA strands — a mandatory fact for NEET questions.

  • DNA is double-stranded and contains deoxyribose sugar; RNA is single-stranded and contains ribose sugar. DNA contains thymine; RNA contains uracil in place of thymine.

  • Common mistake: Many students confuse the functions and deficiency diseases of different vitamins. Vitamin C deficiency causes scurvy; Vitamin D causes rickets; Vitamin B₁ causes beriberi; Vitamin A causes night blindness.

  • Enzymes are biological catalysts that are specific, efficient, and sensitive to temperature and pH. Most enzymes work best around 37°C (body temperature) and neutral pH.

  • Hormones are chemical messengers released in small quantities that regulate body functions. Insulin (protein hormone) regulates blood glucose; adrenaline (amino acid derivative) is released during stress.

  • Starch is a storage polysaccharide in plants; glycogen serves the same function in animals. Cellulose is a structural polysaccharide in plant cell walls and is not digestible by humans.

  • Exam tip: For the CBSE board, prepare a compact table of vitamins, their chemical names, deficiency diseases, and food sources — this is a recurring 3–5 mark question.

  • Lipids are not polymers; they are ester compounds formed from glycerol and fatty acids. Unsaturated fats (with C=C double bonds) are healthier than saturated fats as they do not raise LDL cholesterol levels.

  • The zwitter ionic form of amino acids explains why they have high melting points (exist as ionic crystals) and are soluble in water despite being organic compounds.

  • NEET tip: The entire chapter links directly to Class 12 Biology — studying it from both angles (chemical structure and biological function) significantly boosts overall performance in both subjects.

Detailed Explanation of NCERT Class 12 Chemistry Chapter 10

Biomolecules represents a shift in tone from the rest of Class 12 organic chemistry. Instead of reaction mechanisms and synthetic transformations, this chapter asks a deeper question: how do the structural features of chemical compounds relate to their functions in living systems? The answer, explored through carbohydrates, proteins, nucleic acids, vitamins, and enzymes, reveals a profound logic — one where molecular shape, bonding, and reactivity directly translate into biological activity.

Carbohydrates provide an excellent example of how subtle structural differences carry enormous functional consequences. Starch and cellulose are both polymers of glucose, yet one can be digested and used as energy while the other forms the rigid structural framework of plant cell walls. The only difference lies in the type of glycosidic bond — α in starch, β in cellulose — but that difference is all it takes to make the two molecules as different as food and wood. This level of chemical detail reveals just how precisely molecules are designed by nature.

Proteins add another layer of sophistication. A protein's function is entirely dependent on its three-dimensional shape, which arises from the primary sequence of amino acids through a hierarchy of structural levels. Haemoglobin must have exactly the right quaternary structure to carry oxygen; insulin must fold correctly to regulate blood sugar; enzymes must maintain their precise active site geometry to catalyse reactions. When proteins are denatured — losing their higher-order structure due to heat or pH changes — they lose their biological activity even though their amino acid sequence is unchanged. This illustrates how form and function are inseparable at the molecular level.

Board Exam Tip: For 5-mark questions, be prepared to explain the complete structure of a nucleotide, the double helix model of DNA with base pairing, or the four levels of protein structure with examples. These are the most commonly awarded full-mark answers in this chapter — practise writing them from memory.

Nucleic acids introduce the fascinating chemistry of genetic information. DNA's double helix, stabilised by hydrogen bonds between specific base pairs (A–T with 2 bonds, G–C with 3 bonds), encodes the instructions for building every protein in a living cell. The elegance of this complementary base pairing — where one strand is always a precise mirror of the other — is both chemically logical and biologically essential for faithful replication and transcription.

This chapter connects organically with nearly every other area of science. The vitamins discussed here reappear in nutrition science; the hormone chemistry links to endocrinology; the enzyme chemistry is the foundation of biotechnology and pharmaceutical design. For students heading into medicine, biology, biotechnology, or food science, the concepts learned here form a permanent cornerstone of their future studies — making this chapter one of the most rewarding in the entire Class 12 curriculum.

FAQs – NCERT Solutions for Class 12 Chemistry Chapter 10: Biomolecules

NCERT Solutions for Class 12 Chemistry Chapter 10 Biomolecules