CBSE Class 10 Science Revision Notes Chapter 4 Carbon and Its Compounds 2026–27
CBSE Class 10 Science Revision Notes Chapter 4 cover carbon bonding, hydrocarbons, reactions, ethanol, ethanoic acid and cleansing agents. Carbon and Its Compounds explains why carbon forms many compounds through covalent bonding, tetravalency and catenation in the CBSE Class 10 Science syllabus.
Carbon and Its Compounds studies the bonding, structure and chemical behaviour of carbon compounds. Carbon forms covalent bonds and can join with itself to form long chains, branches and rings. This makes carbon a major element in fuels, food, medicines, soaps, detergents and many daily-use substances.
Use these CBSE Class 10 Science Revision Notes Chapter 4 for the 2026–27 exams to revise definitions, formulas, reactions and important differences. Start with covalent bonding and the versatile nature of carbon, then revise hydrocarbons, functional groups, ethanol, ethanoic acid, soaps and detergents.
Key Takeaways
- Carbon: It has four valence electrons and forms covalent bonds by sharing electrons.
- Tetravalency: Carbon can form four bonds with carbon, hydrogen, oxygen, chlorine and other atoms.
- Catenation: Carbon atoms join together to form straight chains, branched chains and rings.
- Reaction types: Combustion, oxidation, addition and substitution are key chemical reactions in this chapter.
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CBSE Class 10 Science Revision Notes Chapter 4 at a Glance
Carbon and Its Compounds is a chemistry chapter based on bonding, structure and reactions. The chapter connects simple molecular structures with daily-use substances such as fuels, vinegar, soaps and detergents.
| Concept | Definition | Key Term |
| Covalent bond | Bond formed by sharing electrons | Electron sharing |
| Tetravalency | Ability of carbon to form four bonds | Valency of carbon |
| Catenation | Ability of carbon to bond with itself | Carbon chains |
| Hydrocarbons | Compounds of carbon and hydrogen | Alkanes, alkenes, alkynes |
| Functional group | Atom or group deciding compound properties | -OH, -COOH |
| Homologous series | Series with same functional group and formula pattern | -CH₂ difference |
| Micelle | Cluster of soap molecules around oily dirt | Cleansing action |
What are Carbon Compounds?
Carbon compounds are chemical compounds that contain carbon. Most fuels, food materials, medicines, plastics, fibres, soaps and detergents contain carbon.
Carbon forms a large number of compounds because it bonds with itself and other elements. It can form single, double and triple covalent bonds.
| Compound | Formula | Common Example |
| Methane | CH₄ | Fuel |
| Ethane | C₂H₆ | Hydrocarbon |
| Ethene | C₂H₄ | Unsaturated hydrocarbon |
| Ethanol | C₂H₅OH | Alcohol |
| Ethanoic acid | CH₃COOH | Vinegar |
Bonding in Carbon
Carbon has atomic number 6. Its electronic configuration is 2, 4. It has four electrons in its outermost shell.
Carbon cannot easily lose four electrons because that requires high energy. It also cannot easily gain four electrons because the nucleus cannot hold ten electrons strongly. So, carbon shares electrons and forms covalent bonds.
Covalent Bonding in Carbon
A covalent bond is formed when atoms share one or more pairs of electrons. Carbon mainly forms covalent bonds because it needs four more electrons to complete its octet.
| Type of Bond | Electrons Shared | Example |
| Single covalent bond | One pair | H₂, CH₄ |
| Double covalent bond | Two pairs | O₂, C₂H₄ |
| Triple covalent bond | Three pairs | N₂, C₂H₂ |
Covalent bonding in carbon helps form stable molecules such as methane, ethane, ethene and ethyne.
Formation of Covalent Bonds in Common Molecules
Covalent bond formation becomes easier to revise through simple molecules. These examples show how atoms complete their outermost shells by sharing electrons.
Hydrogen Molecule
Each hydrogen atom has one electron. Two hydrogen atoms share one pair of electrons and form H₂.
H - H
Oxygen Molecule
Each oxygen atom has six valence electrons. Two oxygen atoms share two pairs of electrons and form O₂.
O = O
Nitrogen Molecule
Each nitrogen atom has five valence electrons. Two nitrogen atoms share three pairs of electrons and form N₂.
N ≡ N
Methane Molecule
Carbon shares one electron each with four hydrogen atoms. This forms four single covalent bonds in methane.
Formula: CH₄
Properties of Covalent Compounds
Covalent compounds are formed by sharing electrons. They usually have low melting and boiling points because the forces between their molecules are weak.
| Property | Covalent Compounds |
| Bond formation | Sharing of electrons |
| Physical state | Usually gases, liquids or soft solids |
| Melting and boiling points | Generally low |
| Electrical conductivity | Poor conductors |
| Solubility | Often soluble in organic solvents |
| Ions | Do not form ions easily |
Covalent compounds do not conduct electricity because they do not contain free ions.
Versatile Nature of Carbon
The versatile nature of carbon means carbon can form a wide variety of compounds. This happens mainly because of tetravalency and catenation.
Carbon can form bonds with hydrogen, oxygen, nitrogen, sulphur, chlorine and other carbon atoms. It can also form different structures with the same atoms.
Tetravalency of Carbon
Carbon has four valence electrons. It can share all four electrons with other atoms. This property is called tetravalency.
Due to tetravalency, carbon forms four covalent bonds. In methane, one carbon atom forms four single bonds with four hydrogen atoms.
CH₄
Catenation
Catenation is the ability of carbon atoms to bond with other carbon atoms. Carbon shows catenation because carbon-carbon bonds are stable.
Carbon can form straight chains, branched chains and ring structures.
| Structure | Meaning | Example |
| Straight chain | Carbon atoms joined in one line | Butane |
| Branched chain | Side chain attached to main chain | Isobutane |
| Ring structure | Carbon atoms form a closed ring | Cyclohexane |
Catenation explains why carbon compounds exist in large numbers.
Saturated and Unsaturated Hydrocarbons
Hydrocarbons are compounds made of carbon and hydrogen. They are classified based on the type of bond between carbon atoms.
| Basis | Saturated Hydrocarbons | Unsaturated Hydrocarbons |
| Bond type | Single bonds only | Double or triple bonds |
| Main types | Alkanes | Alkenes and alkynes |
| Reactivity | Less reactive | More reactive |
| Common reaction | Substitution | Addition |
| Example | Ethane, C₂H₆ | Ethene, C₂H₄ |
Saturated and unsaturated hydrocarbons are important in Carbon and Its Compounds Class 10 Notes because their reactions are different.
Alkanes, Alkenes and Alkynes
Alkanes, alkenes and alkynes are three main groups of hydrocarbons. Their names and formulas depend on the bonds present between carbon atoms.
| Hydrocarbon | Bond Type | General Formula | Example |
| Alkane | Single bond | CₙH₂ₙ₊₂ | Methane, CH₄ |
| Alkene | Double bond | CₙH₂ₙ | Ethene, C₂H₄ |
| Alkyne | Triple bond | CₙH₂ₙ₋₂ | Ethyne, C₂H₂ |
Alkanes are saturated hydrocarbons. Alkenes and alkynes are unsaturated hydrocarbons.
Chains, Branches and Rings
Carbon atoms can arrange themselves in different ways. This creates different compounds with different structures.
Straight-chain compounds have carbon atoms joined in a continuous line. Branched compounds have side chains attached to the main chain. Ring compounds have carbon atoms joined in a closed structure.
Structural Isomerism
Structural isomerism occurs when compounds have the same molecular formula but different structures.
Example: Butane and isobutane both have the formula C₄H₁₀. Their carbon atoms are arranged differently.
Structural isomerism happens because carbon can form different chains and branches.
Functional Groups
A functional group is an atom or group of atoms that gives a carbon compound its characteristic properties. It decides how the compound reacts.
| Functional Group | Formula | Compound Family | Example |
| Alcohol | -OH | Alcohols | Ethanol |
| Aldehyde | -CHO | Aldehydes | Ethanal |
| Ketone | >C=O | Ketones | Propanone |
| Carboxylic acid | -COOH | Carboxylic acids | Ethanoic acid |
| Halogen | -Cl, -Br, -I | Haloalkanes | Chloromethane |
Functional groups help classify organic compounds in Class 10 Science Chapter 4 Carbon and Its Compounds.
Homologous Series
A homologous series is a group of organic compounds with the same functional group and similar chemical properties. Two successive members differ by a -CH₂ unit.
Example: Alkane series
| Compound | Formula |
| Methane | CH₄ |
| Ethane | C₂H₆ |
| Propane | C₃H₈ |
| Butane | C₄H₁₀ |
Members of a homologous series have similar chemical properties because they contain the same functional group.
Features of a Homologous Series
Homologous series helps organise carbon compounds. It also helps predict formulas and properties of related compounds.
- Members have the same functional group.
- Members have the same general formula.
- Successive members differ by -CH₂.
- Chemical properties are similar.
- Physical properties change gradually with molecular mass.
Nomenclature of Carbon Compounds
Nomenclature means naming carbon compounds using fixed rules. The name depends on the number of carbon atoms, bond type and functional group.
| Number of Carbon Atoms | Word Root |
| 1 | Meth |
| 2 | Eth |
| 3 | Prop |
| 4 | But |
| 5 | Pent |
| 6 | Hex |
Suffix Based on Bond Type
The suffix tells the type of bond present in the carbon chain.
| Bond Type | Suffix | Example |
| Single bond | -ane | Ethane |
| Double bond | -ene | Ethene |
| Triple bond | -yne | Ethyne |
Suffix Based on Functional Group
The functional group changes the ending of the compound name.
| Functional Group | Suffix | Example |
| Alcohol | -ol | Ethanol |
| Aldehyde | -al | Ethanal |
| Ketone | -one | Propanone |
| Carboxylic acid | -oic acid | Ethanoic acid |
Chemical Properties of Carbon Compounds
Carbon compounds show different reactions based on their bonding and functional groups. The main reactions are combustion, oxidation, addition and substitution.
These reactions are important in Class 10 Chemistry Chapter 4 Notes because they often appear in reasoning questions.
Combustion
Combustion is the burning of a substance in oxygen to produce heat and light. Carbon compounds burn in oxygen to form carbon dioxide and water.
General reaction:
Carbon compound + O₂ → CO₂ + H₂O + Heat + Light
Example:
CH₄ + 2O₂ → CO₂ + 2H₂O + Heat
Saturated hydrocarbons usually burn with a clean flame. Unsaturated hydrocarbons often burn with a yellow, smoky flame.
Oxidation
Oxidation is a reaction in which oxygen is added to a substance. Ethanol can be oxidised to ethanoic acid.
CH₃CH₂OH + Oxygen → CH₃COOH + H₂O
Oxidising agents such as alkaline potassium permanganate or acidified potassium dichromate are used for this reaction.
Addition Reaction
Addition reactions occur in unsaturated hydrocarbons. In these reactions, atoms are added across a double or triple bond.
Example:
Ethene + Hydrogen → Ethane
C₂H₄ + H₂ → C₂H₆
This reaction takes place in the presence of a catalyst such as nickel.
Substitution Reaction
Substitution reaction occurs when one atom replaces another atom in a compound. Alkanes usually show substitution reactions.
Example:
CH₄ + Cl₂ → CH₃Cl + HCl
Condition: Sunlight
In this reaction, chlorine replaces one hydrogen atom of methane.
Combustion, Oxidation, Addition and Substitution Reactions
| Reaction | Shown By | Key Point | Example |
| Combustion | Carbon compounds | Burns in oxygen | CH₄ + 2O₂ → CO₂ + 2H₂O |
| Oxidation | Alcohols | Oxygen is added | Ethanol → Ethanoic acid |
| Addition | Unsaturated hydrocarbons | Atoms add across double or triple bond | C₂H₄ + H₂ → C₂H₆ |
| Substitution | Saturated hydrocarbons | One atom replaces another | CH₄ + Cl₂ → CH₃Cl + HCl |
Reactions of Ethanol and Ethanoic Acid
Ethanol and ethanoic acid are two important carbon compounds. Their formulas, properties and reactions are frequently asked in CBSE Notes Class 10 Science Chapter 4.
Ethanol
Ethanol is an alcohol with the formula C₂H₅OH. It is a colourless liquid with a pleasant smell.
| Property | Ethanol |
| Formula | C₂H₅OH |
| Functional group | -OH |
| State | Liquid |
| Solubility | Soluble in water |
| Litmus effect | Neutral |
| Conductivity | Poor conductor |
Uses of Ethanol
Ethanol is used as a solvent in medicines, paints and perfumes. It is also used in tincture iodine and as a fuel mixture with petrol.
Ethanol is present in alcoholic drinks. Large amounts affect the nervous system and damage health.
Reaction of Ethanol with Sodium
Ethanol reacts with sodium to form sodium ethoxide and hydrogen gas.
2C₂H₅OH + 2Na → 2C₂H₅ONa + H₂
Hydrogen gas is released during this reaction.
Dehydration of Ethanol
When ethanol is heated with concentrated sulphuric acid at 443 K, it forms ethene.
CH₃CH₂OH → CH₂=CH₂ + H₂O
Condition: Concentrated H₂SO₄, 443 K
This reaction is called dehydration because water is removed.
Ethanoic Acid
Ethanoic acid is a carboxylic acid with the formula CH₃COOH. Its common name is acetic acid.
A 5-8% solution of ethanoic acid in water is called vinegar.
| Property | Ethanoic Acid |
| Formula | CH₃COOH |
| Common name | Acetic acid |
| Functional group | -COOH |
| Nature | Acidic |
| Dilute form | Vinegar |
| Pure form | Glacial acetic acid |
Pure ethanoic acid freezes in cold weather and forms ice-like crystals.
Reactions of Ethanoic Acid
Ethanoic acid reacts with bases, carbonates and bicarbonates. These reactions help identify carboxylic acids.
Reaction with Sodium Hydroxide
CH₃COOH + NaOH → CH₃COONa + H₂O
This is a neutralisation reaction.
Reaction with Sodium Carbonate
2CH₃COOH + Na₂CO₃ → 2CH₃COONa + H₂O + CO₂
Carbon dioxide gas is released.
Reaction with Sodium Bicarbonate
CH₃COOH + NaHCO₃ → CH₃COONa + H₂O + CO₂
The brisk effervescence shows the release of carbon dioxide gas.
Esterification
Esterification is the reaction between an alcohol and a carboxylic acid to form an ester. Esters have a pleasant smell.
CH₃COOH + C₂H₅OH → CH₃COOC₂H₅ + H₂O
Condition: Concentrated H₂SO₄
Ethanoic acid and ethanol form ethyl ethanoate during esterification.
Saponification
Saponification is the alkaline hydrolysis of an ester to form soap and alcohol.
General reaction:
Ester + Sodium hydroxide → Sodium salt of carboxylic acid + Alcohol
This reaction is used in soap-making.
Soaps and Detergents
Soaps and detergents are cleansing agents. They remove dirt and grease from surfaces such as skin and clothes.
Soap is a sodium or potassium salt of a long-chain carboxylic acid. Detergents are cleansing agents that work better in hard water.
Structure of Soap Molecule
A soap molecule has two parts. One part dissolves in oil, while the other dissolves in water.
| Part of Soap Molecule | Nature | Attracted To |
| Hydrocarbon tail | Hydrophobic | Oil and grease |
| Ionic head | Hydrophilic | Water |
The hydrophobic tail attaches to oily dirt. The hydrophilic head remains attached to water.
Cleansing Action of Soap
When soap is added to water, soap molecules arrange around oily dirt. Their tails move into oil, while their heads face water.
This forms a spherical structure called a micelle. On rinsing, micelles carry dirt and grease away with water.
What is a Micelle?
A micelle is a cluster of soap molecules formed around oily dirt in water. The hydrophobic tails stay inside, while the hydrophilic heads stay outside.
Micelles help remove oil and grease from clothes and skin.
Why Soap Does Not Work Well in Hard Water
Hard water contains calcium and magnesium salts. These salts react with soap and form an insoluble substance called scum.
2C₁₇H₃₅COONa + CaCl₂ → (C₁₇H₃₅COO)₂Ca + 2NaCl
Scum reduces lather and wastes soap. It also makes cleaning less effective.
Difference Between Soaps and Detergents
Soaps and detergents both clean surfaces, but they behave differently in hard water.
| Basis | Soaps | Detergents |
| Composition | Sodium or potassium salts of fatty acids | Usually salts of sulphonic acids |
| Hard water action | Form scum | Do not form scum easily |
| Cleaning in hard water | Less effective | More effective |
| Source | Oils and fats | Petroleum-based chemicals |
| Biodegradability | Usually biodegradable | Some may not be biodegradable |
Important Formulas from CBSE Notes Class 10 Science Chapter 4
These formulas are useful for quick revision before solving chapter questions.
| Compound | Formula |
| Methane | CH₄ |
| Ethane | C₂H₆ |
| Ethene | C₂H₄ |
| Ethyne | C₂H₂ |
| Ethanol | C₂H₅OH |
| Ethanoic acid | CH₃COOH |
| Sodium ethoxide | C₂H₅ONa |
| Ethyl ethanoate | CH₃COOC₂H₅ |
Important Reactions from Class 10 Science Chapter 4
These equations cover the main reaction types in Carbon and Its Compounds Notes.
| Reaction | Equation |
| Combustion of methane | CH₄ + 2O₂ → CO₂ + 2H₂O |
| Chlorination of methane | CH₄ + Cl₂ → CH₃Cl + HCl |
| Ethanol with sodium | 2C₂H₅OH + 2Na → 2C₂H₅ONa + H₂ |
| Dehydration of ethanol | CH₃CH₂OH → CH₂=CH₂ + H₂O |
| Ethanoic acid with NaOH | CH₃COOH + NaOH → CH₃COONa + H₂O |
| Ethanoic acid with NaHCO₃ | CH₃COOH + NaHCO₃ → CH₃COONa + H₂O + CO₂ |
| Esterification | CH₃COOH + C₂H₅OH → CH₃COOC₂H₅ + H₂O |
How to Identify Reaction Types in Carbon Compounds
Questions in this chapter often give a condition or product. Use the clue to identify the reaction type.
| Clue in Question | Reaction Type |
| Compound burns in oxygen | Combustion |
| Ethanol changes into ethanoic acid | Oxidation |
| Hydrogen adds to ethene | Addition |
| Chlorine replaces hydrogen in methane | Substitution |
| Alcohol reacts with carboxylic acid | Esterification |
| Ester reacts with sodium hydroxide | Saponification |
Difference Between Key Concepts in Carbon and Its Compounds
Difference-based questions are common in Class 10 Science Chapter 4 Notes. Revise these pairs before practising answers.
| Topic | Difference |
| Saturated and unsaturated hydrocarbons | Saturated hydrocarbons have single bonds; unsaturated hydrocarbons have double or triple bonds. |
| Alkane and alkene | Alkanes have single bonds; alkenes have at least one double bond. |
| Ethanol and ethanoic acid | Ethanol is an alcohol; ethanoic acid is a carboxylic acid. |
| Addition and substitution | Addition occurs in unsaturated compounds; substitution occurs in saturated compounds. |
| Soap and detergent | Soap forms scum in hard water; detergent does not form scum easily. |
Common Exam Questions from Carbon and Its Compounds
These question types help revise the scoring parts of Class 10 Science Chapter 4 Carbon and Its Compounds.
Q1. Why does carbon form covalent bonds?
Carbon has four valence electrons. It cannot easily lose or gain four electrons. So, it shares electrons with other atoms and forms covalent bonds.
Q2. What are tetravalency and catenation?
Tetravalency is the ability of carbon to form four covalent bonds. Catenation is the ability of carbon to bond with itself and form chains, branches and rings.
Q3. What is the difference between saturated and unsaturated hydrocarbons?
Saturated hydrocarbons contain only single bonds between carbon atoms. Unsaturated hydrocarbons contain double or triple bonds between carbon atoms.
Q4. What is a homologous series?
A homologous series is a group of organic compounds with the same functional group and similar chemical properties. Two successive members differ by -CH₂.
Q5. Why are detergents more effective than soaps in hard water?
Detergents do not form scum with calcium and magnesium ions in hard water. So, they clean better than soaps in hard water.
Solved Questions from Carbon and Its Compounds Class 10
Solved examples help connect definitions with reactions and exam-style answers.
Example 1: Why does carbon form a large number of compounds?
Carbon forms a large number of compounds because it shows tetravalency and catenation. It can form four covalent bonds and can join with other carbon atoms. This allows carbon to form chains, branches and rings.
Example 2: Write the reaction of ethanol with sodium.
Ethanol reacts with sodium to form sodium ethoxide and hydrogen gas.
2C₂H₅OH + 2Na → 2C₂H₅ONa + H₂
Example 3: Why are unsaturated hydrocarbons more reactive?
Unsaturated hydrocarbons contain double or triple bonds. These bonds can open up during addition reactions. So, unsaturated hydrocarbons are more reactive than saturated hydrocarbons.
Example 4: What happens when ethanoic acid reacts with sodium bicarbonate?
Ethanoic acid reacts with sodium bicarbonate to form sodium ethanoate, water and carbon dioxide.
CH₃COOH + NaHCO₃ → CH₃COONa + H₂O + CO₂
Brisk effervescence occurs due to carbon dioxide gas.
Example 5: Why does soap form scum in hard water?
Hard water contains calcium and magnesium ions. These ions react with soap and form insoluble salts called scum. Scum reduces lather and cleaning action.
CBSE Class 10 Science Chapter 4 Carbon and Its Compounds Summary
Carbon and Its Compounds explains how carbon forms covalent bonds through electron sharing. Carbon shows tetravalency and catenation, which help it form many compounds.
The chapter covers saturated and unsaturated hydrocarbons, functional groups, homologous series and nomenclature. It also explains chemical reactions such as combustion, oxidation, addition and substitution.
Ethanol, ethanoic acid, esterification, saponification, soaps and detergents are important scoring areas. Students can revise formulas, equations, differences and definitions from these notes before practising NCERT questions.
Useful Links for Class 10 Science
| Section | Useful Links |
| NCERT Solutions | NCERT Solutions for Class 10 Science |
| Important Questions | Important Questions Class 10 Science |
| Previous Year Papers | CBSE Science Question Paper Class 10 |
| NCERT Books | NCERT Books for Class 10 Science |
| Revision Notes | CBSE Class 10 Science Revision Notes |
| Syllabus | CBSE Class 10 Science Syllabus |
| Sample Papers | CBSE Sample Papers for Class 10 Science |
CBSE Class 10 Science Revision Notes
FAQs (Frequently Asked Questions)
Carbon forms many compounds because it shows tetravalency and catenation. Tetravalency allows carbon to form four bonds. Catenation allows carbon atoms to join together and form long chains, branches and rings.
Alkanes contain only single bonds between carbon atoms. Alkenes contain at least one double bond. Alkynes contain at least one triple bond between carbon atoms.
Pure ethanoic acid is called glacial acetic acid because it freezes in cold weather. It forms ice-like crystals when the temperature falls below its melting point.
Esterification is the reaction between an alcohol and a carboxylic acid. It forms a sweet-smelling ester and water in the presence of concentrated sulphuric acid.
Soaps react with calcium and magnesium ions in hard water. This forms insoluble scum, which reduces lather and cleaning action.
