NCERT Solutions for Class 10 Science Chapter 4: Carbon and Its Compounds
Carbon and Its Compounds is widely regarded as one of the most interesting yet challenging chapters in Class 10 Science. The reason is simple — carbon forms the backbone of all living matter and millions of organic compounds. This chapter takes students into the world of organic chemistry, covering the unique nature of carbon, its covalent bonding, the concept of chains, branches, and rings, functional groups, homologous series, nomenclature of carbon compounds, and the chemical properties of ethanol and ethanoic acid. NCERT Solutions for Class 10 Science Chapter 4 on Myclass24 are detailed, example-based, and follow CBSE guidelines rigorously.
Understanding carbon's tetravalency and catenation is crucial — and these properties are the basis for thousands of questions in board exams and entrance tests alike. This chapter also covers soaps, detergents, micelle formation, and the difference between hard water and soft water — practical topics with real-world connections that students find fascinating.
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Chapter 4 Concepts and Quick Tables: Carbon and Its Compounds
Carbon Chemistry can be overwhelming without a structured approach. The tables and explanations below break down Chapter 4 into manageable chunks for quick revision, whether you are studying on a phone, tablet, or laptop.
Why Is Carbon So Special? Key Properties
| Property | Explanation | Result |
|---|---|---|
| Tetravalency | Carbon has 4 valence electrons | Can form 4 bonds with other atoms |
| Catenation | Carbon bonds with other carbon atoms | Long chains, branched chains, rings |
| Small atom size | Strong bonds with C, H, O, N, S | Millions of stable compounds |
| Forms multiple bonds | Single, double, and triple bonds | Wide variety of compound types |
Functional Groups in Organic Chemistry
| Functional Group | Formula | Class of Compound | Example |
|---|---|---|---|
| Alcohol | –OH | Alcohols | Ethanol (C₂H₅OH) |
| Aldehyde | –CHO | Aldehydes | Methanal (HCHO) |
| Ketone | –CO– | Ketones | Propanone (CH₃COCH₃) |
| Carboxylic Acid | –COOH | Acids | Ethanoic acid (CH₃COOH) |
| Halogens | –Cl / –Br | Haloalkanes | Chloromethane (CH₃Cl) |
Homologous Series — Features and Example
A homologous series is a group of organic compounds that have the same functional group, same general formula, similar chemical properties, and differ by a –CH₂– unit (molecular mass difference of 14 u). For example, the alkane series: Methane (CH₄) → Ethane (C₂H₆) → Propane (C₃H₈) → Butane (C₄H₁₀).
Properties of Ethanol and Ethanoic Acid
| Property | Ethanol (C₂H₅OH) | Ethanoic Acid (CH₃COOH) |
|---|---|---|
| Nature | Alcohol | Carboxylic acid |
| Smell | Pleasant smell | Vinegar-like smell |
| Reaction with Na | Releases H₂ gas | Releases H₂ gas |
| pH | Neutral (~7) | Acidic (~3) |
| Ester formation | Forms ester with acid | Forms ester with alcohol |
| Use | Beverages, fuel, sanitiser | Vinegar, preservatives, solvent |
Soaps vs Detergents — Key Differences
| Aspect | Soaps | Detergents |
|---|---|---|
| Made from | Fats/oils + NaOH (saponification) | Petrochemicals |
| Works in hard water | No (forms scum) | Yes (no scum) |
| Biodegradable | Yes | Some are non-biodegradable |
| Cost | Generally cheaper | More expensive |
| Uses | Bathing, skin care | Laundry, dishwashing |
FAQs for NCERT Solutions for Class 10 Science Chapter 4 Carbon and its Compounds
A covalent bond is formed when two atoms share a pair of electrons to achieve a stable electron configuration, typically by completing their outermost shell. Carbon has four electrons in its outermost shell and needs four more to complete it. Carbon cannot form ionic bonds by gaining or losing four electrons because it would require too much energy. Instead, carbon shares electrons with other atoms, forming strong and stable covalent bonds. Carbon can form single, double, or triple covalent bonds. For example, methane (CH₄) has four single bonds, ethylene (C₂H₄) has one double bond between carbons, and acetylene (C₂H₂) has a triple bond. This ability to form multiple bonds makes carbon the backbone of organic chemistry.
Saturated hydrocarbons contain only single bonds between carbon atoms and are called alkanes. They are considered saturated because each carbon is bonded to the maximum number of hydrogen atoms possible. Examples include methane (CH₄), ethane (C₂H₆), and propane (C₃H₈). Unsaturated hydrocarbons contain at least one double or triple bond between carbon atoms. Those with double bonds are alkenes (like ethene, C₂H₄) and those with triple bonds are alkynes (like ethyne, C₂H₂). Unsaturated compounds are more reactive than saturated ones and can undergo addition reactions where hydrogen, halogens, or other small molecules are added across the double or triple bond. Vegetable oils are unsaturated fats while animal fats like butter are saturated.
Ethanol (C₂H₅OH), commonly called alcohol, is a colourless liquid with a pleasant smell and low boiling point of 78°C. It is miscible with water in all proportions. Ethanol is used as a solvent in medicines, perfumes, and paints. It is the alcohol present in alcoholic beverages and is also used as a fuel additive. When ethanol burns, it produces carbon dioxide and water. Ethanoic acid (CH₃COOH), commonly called acetic acid or vinegar (when dilute), has a sour taste and a pungent smell. Its melting point is 17°C, so it freezes in cold weather earning it the name glacial acetic acid. It is used in preserving food, making vinegar, and as a solvent. Both compounds are important in everyday life and industrial processes.
A homologous series is a group of organic compounds that have the same general formula, similar chemical properties, and show a gradation in physical properties with each successive member differing by a CH₂ unit. For example, the alkane series: methane (CH₄), ethane (C₂H₆), propane (C₃H₈), and butane (C₄H₁₀) — each differs by one CH₂ group. Key characteristics include: successive members differ by 14 atomic mass units (one CH₂ unit), all members can be represented by a single general formula, they have similar chemical reactions, and their physical properties like boiling point, melting point, and density change gradually. This gradation helps predict the properties of unknown members and makes studying organic chemistry more systematic and organised.
Saponification is the chemical reaction in which a fat or oil (ester) reacts with a strong base like sodium hydroxide or potassium hydroxide to produce soap (sodium or potassium salt of fatty acid) and glycerol. The word saponification literally means soap making. When vegetable oil or animal fat is heated with concentrated NaOH solution, the ester bonds in the triglycerides break down, releasing glycerol and long-chain fatty acid salts — which are soaps. Sodium soaps are hard soaps used for bathing and washing, while potassium soaps are soft soaps used in shaving creams and liquid soaps. Soap cleans because one end of the molecule (hydrophilic head) attracts water while the other end (hydrophobic tail) attracts oil and grease, forming micelles that trap dirt particles.




