Biomolecules Class 12 PDF: Comprehensive NEET Study Guide

01
Introduction to biomolecules class 12 chemistry

Mastering the concepts of biomolecules class 12 chemistry is fundamental for any medical aspirant aiming to excel in NEET. Biomolecules are the organic compounds that form the basis of life, driving the complex chemical processes within living organisms. From providing energy through carbohydrates to carrying genetic information via nucleic acids, these molecules are the building blocks of every biological entity. In this guide, we provide a high-yield summary of the entire chapter to boost your NEET percentile.

Living systems are composed of various complex organic compounds such as carbohydrates, proteins, enzymes, lipids, vitamins, and nucleic acids. These molecules interact with each other and constitute the molecular logic of life processes. Understanding their structure, classification, and chemical properties is a major focus area for competitive entrance examinations.

CHEMICAL NATURE Most biomolecules are polymers or complex structures consisting of smaller repeating units called monomers.
IMPORTANCE They provide energy, structural support, biological catalysis, and help in the transmission of hereditary traits.

02
Classification in biomolecules class 12 chemistry: Carbohydrates

Carbohydrates, also known as saccharides, are polyhydroxy aldehydes or ketones or compounds which produce them on hydrolysis. They are the most abundant biomolecules on Earth and serve as the primary energy source for most organisms.

Class Definition Examples
Monosaccharides Cannot be hydrolyzed further into simpler units. Glucose, Fructose, Ribose
Oligosaccharides Yield 2 to 10 monosaccharide units on hydrolysis. Sucrose, Maltose, Lactose
Polysaccharides Large polymers yielding many monosaccharide units. Starch, Cellulose, Glycogen

Structure and Reactions of Glucose

Glucose (C6H12O6) is an aldohexose. Its structure consists of an aldehyde group and five hydroxyl groups. In aqueous solution, it predominantly exists in cyclic forms known as α-D-glucopyranose and β-D-glucopyranose.

KEY OXIDATION REACTION
Glucose + Bromine Water → Gluconic Acid
Glucose + Conc. HNO3 → Saccharic Acid
TIP
Sucrose is a non-reducing sugar because the reducing groups of glucose and fructose are involved in glycosidic bond formation. Maltose and Lactose are reducing sugars.
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03
Proteins and Amino Acids

Proteins are the most versatile biomolecules class 12 chemistry students study. They are polymers of α-amino acids linked by peptide bonds. Amino acids contain both an amino (−NH2) and a carboxyl (−COOH) group attached to the same carbon atom.

ZWITTER ION FORMATION
H2N−CH(R)−COOH ↔ H3N+−CH(R)−COO

(In neutral solution, amino acids exist as dipolar ions called Zwitterions.)

Classification of Amino Acids

  • Essential: Cannot be synthesized by the body; must be taken through diet (e.g., Valine, Leucine).
  • Non-essential: Can be synthesized by the body (e.g., Glycine, Alanine).
  • Acidic: Contain extra −COOH (Aspartic acid).
  • Basic: Contain extra −NH2 (Lysine).

04
Structural Levels of Proteins

The complexity of protein architecture is divided into four levels. This is a high-yield conceptual area for biomolecules class 12 chemistry MCQ practice.

PRIMARY STRUCTURE The linear sequence of amino acids in a polypeptide chain. Any change here can cause diseases like Sickle Cell Anemia.
SECONDARY STRUCTURE Folding due to H-bonding into α-helix or β-pleated sheets.
TERTIARY STRUCTURE Overall 3D folding involving disulfide, ionic, and hydrophobic interactions. It determines biological activity.
QUATERNARY STRUCTURE Spatial arrangement of multiple polypeptide subunits (e.g., Hemoglobin).
WARN
Denaturation: Exposure to heat or pH change disrupts secondary and tertiary structures but leaves the primary sequence intact. The protein loses its biological activity.

05
Vitamins and Deficiency Diseases

Vitamins are essential micronutrients required in small amounts for normal growth and health. A detailed table of vitamins is a staple for any biomolecules class 12 chemistry student.

Vitamin Solubility Deficiency Disease
Vitamin A (Retinol) Fat Soluble Xerophthalmia, Night Blindness
Vitamin D (Calciferol) Fat Soluble Rickets (children), Osteomalacia
Vitamin C (Ascorbic Acid) Water Soluble Scurvy (bleeding gums)
Vitamin B12 Water Soluble Pernicious Anemia
Vitamin K Fat Soluble Increased blood clotting time
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06
Nucleic Acids in biomolecules class 12 chemistry

Nucleic acids are the biopolymers responsible for the storage and transmission of genetic information. There are two types: DNA (Deoxyribonucleic acid) and RNA (Ribonucleic acid). They are composed of nucleotides, which consist of a pentose sugar, a nitrogenous base, and a phosphate group.

NUCLEOTIDE COMPONENTS
Nucleoside = Sugar + Base
Nucleotide = Sugar + Base + Phosphate

DNA vs RNA

  • Sugar: DNA has 2-deoxyribose; RNA has ribose.
  • Bases: DNA uses Adenine, Guanine, Cytosine, and Thymine. RNA uses Uracil instead of Thymine.
  • Structure: DNA is a double helix; RNA is usually single-stranded.
  • Base Pairing: A pairs with T (2 H-bonds) and G pairs with C (3 H-bonds) in DNA.

07
Enzymes and Hormones

Enzymes are biological catalysts that speed up chemical reactions with incredible specificity. They generally work by lower the activation energy of a reaction through the “Lock and Key” mechanism.

ENZYME ACTION
E + S → [ES] → E + P

Hormones are chemical messengers produced in ductless glands and transported by blood to target organs. They help maintain biological balance (homeostasis). Examples include insulin (regulates blood sugar) and adrenaline (prepares body for stress).

Quick Revision Summary

  • Carbohydrates: General formula Cx(H2O)y. Classified into mono, oligo, and polysaccharides.
  • Glucose: An aldohexose; reduces Tollens’ and Fehling’s reagents.
  • Sucrose: Invert sugar; gives glucose and fructose on hydrolysis.
  • Glycosidic Linkage: Bond between two monosaccharide units through oxygen.
  • Amino Acids: Bifunctional molecules; α-amino acids build proteins.
  • Peptide Bond: −CO−NH− linkage between amino acids.
  • Fibrous Proteins: Water-insoluble (Keratin, Myosin).
  • Globular Proteins: Water-soluble (Insulin, Albumin).
  • DNA bases: A, G, C, T. RNA bases: A, G, C, U.
  • Vitamin C: Heat-labile; must be supplemented daily as it is water-soluble.
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08
Frequently Asked Questions

What is the difference between a nucleoside and a nucleotide?
A nucleoside is formed when a nitrogenous base is attached to the 1′ position of a pentose sugar. When a phosphoric acid group is further attached to the 5′ position of the sugar in a nucleoside, it becomes a nucleotide. Nucleotides are the monomers of nucleic acids.
Why is sucrose called invert sugar?
Sucrose is dextrorotatory (+66.5°). On hydrolysis, it gives an equimolar mixture of D-glucose (+52.5°) and D-fructose (−92.4°). Since the resulting mixture is levorotatory, the sign of rotation has “inverted,” giving it the name invert sugar.
What happens during the denaturation of proteins?
During denaturation, physical or chemical changes (like heat or pH) disrupt the hydrogen bonds and other attractive forces holding the secondary and tertiary structures. The protein uncoils, loses its 3D shape, and becomes biologically inactive, though the primary structure remains intact.
Why are vitamins A, D, E, and K called fat-soluble?
These vitamins are soluble in organic solvents and lipids but insoluble in water. They are stored in the liver and adipose (fat-storing) tissues of the body. Because they are stored, excessive intake can lead to hypervitaminosis.
What is a glycosidic linkage?
A glycosidic linkage is an ether linkage formed between two monosaccharide units through an oxygen atom, following the loss of a water molecule. It is the bond that joins individual sugar units to form disaccharides and polysaccharides.
How do enzymes differ from inorganic catalysts?
Enzymes are highly specific (one enzyme for one reaction), function optimally at body temperature (37°C) and neutral pH, and are significantly more efficient than inorganic catalysts. Unlike inorganic catalysts, they are made of proteins.

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Table of Contents — Chemistry Class 12

Table of Contents

Chemistry — Class 12

01SolutionsGo to page
02ElectrochemistryGo to page
03Chemical KineticsGo to page
04d- and f-Block ElementsGo to page
05Coordination CompoundsGo to page
06Haloalkanes and HaloarenesGo to page
07Alcohols, Phenols and EthersGo to page
08Aldehydes, Ketones and Carboxylic AcidsGo to page
09AminesGo to page
10BiomoleculesGo to page

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