Official Class 10 Science Revision Material: CBSE Class 10 Science Carbon and its Compounds Notes Set 06
Access comprehensive revision notes for Chapter 04 Carbon and Its Compounds using the CBSE Class 10 Science Carbon and its Compounds Notes Set 06. Designed to align with the 2026-27 academic syllabus for Class 10 Science, these concept summaries help students streamline their exam preparation and review complex topics efficiently.
Chapter-wise Concept Summaries: Chapter 04 Carbon and Its Compounds
View or download the dedicated Chapter 04 Carbon and Its Compounds revision resource below. Engaging with these structured concept notes daily ensures continuous academic progress and mastery of the 2026-27 curriculum for Science.
1. Bonding in carbon
Carbon has four electrons in its outer shell (atomic number 6, configuration 2, 4). It cannot easily lose or gain four electrons, so it shares them and forms covalent bonds. A covalent bond is a shared pair of electrons. Examples are methane CH4, ethene C2H4 (a double bond) and ethyne C2H2 (a triple bond). Covalent compounds usually have low melting and boiling points and are poor conductors of electricity.
2. Versatile nature of carbon
Carbon forms a huge number of compounds for two reasons. Catenation is the ability of carbon atoms to join with each other in long chains, branched chains and rings. Tetravalency lets each carbon bond with four other atoms such as hydrogen, oxygen, nitrogen, sulphur and halogens. The small size of carbon makes its bonds strong and stable. Allotropes of carbon include diamond (each atom bonded to four others, very hard), graphite (layers of hexagons, soft and conducting) and fullerene (C-60, football shaped).
3. Hydrocarbons and isomerism
Hydrocarbons contain only carbon and hydrogen. Saturated hydrocarbons (alkanes, CnH2n+2) have only single bonds. Unsaturated hydrocarbons have double bonds (alkenes, CnH2n) or triple bonds (alkynes, CnH2n−2). Compounds with the same molecular formula but different structures are isomers. Butane has two isomers while pentane has three.
4. Functional groups and homologous series
A functional group is an atom or group of atoms that decides the chemical properties of a compound. Common ones are halo (−Cl, −Br), alcohol (−OH), aldehyde (−CHO), ketone (C=O inside the chain) and carboxylic acid (−COOH).
A homologous series is a family of compounds with the same functional group and similar chemical properties in which successive members differ by a CH2 unit (14 u). Physical properties such as boiling point change gradually along the series. Examples: methane, ethane, propane, butane.
5. Nomenclature
1. Count the carbon atoms in the longest chain: 1 meth, 2 eth, 3 prop, 4 but, 5 pent, 6 hex.
2. Add the ending: ane for single bonds, ene for a double bond, yne for a triple bond.
3. For a functional group, replace the final e of the name with its suffix: ol (alcohol), al (aldehyde), one (ketone), oic acid (carboxylic acid). A halogen is a prefix, for example chloropropane.
Examples: CH3OH is methanol, CH3CH2OH is ethanol, CH3CHO is ethanal, CH3COCH3 is propanone, CH3COOH is ethanoic acid.
6. Chemical reactions of carbon compounds
1. Combustion: carbon compounds burn in oxygen to give CO2, water, heat and light. CH4 + 2O2 → CO2 + 2H2O. Saturated hydrocarbons burn with a clean blue flame, while unsaturated ones burn with a yellow sooty flame.
2. Oxidation: alcohols are oxidised to carboxylic acids using alkaline KMnO4 or acidified K2Cr2O7.
3. Addition: unsaturated hydrocarbons add hydrogen in the presence of nickel or palladium catalyst, for example CH2=CH2 + H2 → CH3CH3. This is used to make vegetable ghee from oils.
4. Substitution: saturated hydrocarbons react with chlorine in sunlight, replacing hydrogen: CH4 + Cl2 → CH3Cl + HCl.
7. Ethanol and ethanoic acid
Ethanol is a colourless liquid that is soluble in water and used in medicines, tonics and as a solvent and fuel. It reacts with sodium to give hydrogen: 2CH3CH2OH + 2Na → 2CH3CH2ONa + H2. Heating with concentrated sulphuric acid at 443 K removes water and gives ethene (dehydration). Alcohol meant for industrial use is made unfit to drink by adding methanol and a dye, called denatured alcohol.
Ethanoic acid (acetic acid, 5 to 8 percent solution is vinegar) freezes at 290 K to glacial acetic acid. It is a weak acid. It reacts with carbonates and hydrogencarbonates to release CO2. With ethanol and a few drops of concentrated sulphuric acid it forms a sweet-smelling ester: CH3COOH + C2H5OH → CH3COOC2H5 + H2O. Alkaline hydrolysis of an ester is called saponification and gives soap.
8. Soaps and detergents
Soap is the sodium or potassium salt of a long chain fatty acid. A soap molecule has a water-loving ionic head and a water-hating hydrocarbon tail. In water, soap forms spherical clusters called micelles with tails pointing inward around the grease, which lifts the dirt away. Soaps form an insoluble scum with calcium and magnesium salts in hard water, but detergents (sodium salts of sulphonic acids) do not, so they work well even in hard water.
Worked examples
Example 1. Name the compound CH3CH2CH2CHO.
The chain has 4 carbons, so the base is butane. The group is an aldehyde, so the final e is replaced by al. The name is butanal.
Example 2. How many covalent bonds are present in one molecule of propane, C3H8?
There are 2 carbon to carbon bonds and 8 carbon to hydrogen bonds. The total is 10 single covalent bonds, which equals 3n + 1 for n = 3.
Example 3. A compound A, C2H6O, gives C2H4 (B) on heating with concentrated H2SO4, and B gives C2H6 (C) on adding hydrogen. Identify A, B, C.
A is ethanol, which loses a molecule of water to give ethene (B). Ethene adds hydrogen over a nickel catalyst to give ethane (C). Concentrated sulphuric acid acts as the dehydrating agent.
Quick Check Questions
Answer these five questions to test your understanding of the chapter.
Q1. Which of these is a saturated hydrocarbon: C2H4, C2H6, C3H4, C3H6? [1 mark]
View Answer & Explanation
Answer: C2H6 (ethane), because it fits the general formula CnH2n+2 for alkanes.
Teacher's Note:
1. Saturated hydrocarbons contain only single bonds between carbon atoms.
2. The other three have double or triple bonds or a ring.
Q2. Why do carbon compounds generally have low melting and boiling points and do not conduct electricity? [2 marks]
View Answer & Explanation
Answer: Carbon compounds are covalent, so the forces between their molecules are weak and little energy is needed to separate them. They contain no ions or free electrons, so they do not conduct electricity.
Teacher's Note:
1. Covalent compounds share electrons and do not form ions.
2. Graphite is an exception because it has free electrons.
Q3. Write the structural formulae of the two isomers of butane. [2 marks]
View Answer & Explanation
Answer: Butane has the molecular formula C4H10. The isomers are straight chain n-butane, CH3-CH2-CH2-CH3, and branched isobutane (2-methylpropane), CH3-CH(CH3)-CH3.
Teacher's Note:
1. Isomers have the same molecular formula but different structures.
2. Branching of the chain gives the second isomer.
Q4. An organic compound with molecular formula C2H4O2 gives brisk effervescence with sodium hydrogencarbonate. Identify it, name the gas and write the equation. [3 marks]
View Answer & Explanation
Answer: The compound is ethanoic acid, CH3COOH. The gas is carbon dioxide, which turns lime water milky. CH3COOH + NaHCO3 → CH3COONa + H2O + CO2.
Teacher's Note:
1. Brisk effervescence with a hydrogencarbonate is the standard test for a carboxylic acid.
2. The salt formed is sodium ethanoate.
Q5. Why is the conversion of ethanol to ethanoic acid an oxidation reaction? [2 marks]
View Answer & Explanation
Answer: Ethanol gains oxygen when it is treated with an oxidising agent such as alkaline potassium permanganate or acidified potassium dichromate. CH3CH2OH → CH3COOH, so it is oxidised.
Teacher's Note:
1. Gain of oxygen means oxidation.
2. The oxidising agent itself is reduced in the process.
Free study material for Science
Revision Notes and Key Concepts for Class 10 Science Chapter 04 Carbon and Its Compounds
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