Carbon and Its Compounds — Important Questions & Answers

Welcome to the complete collection of Class 10 Science Chapter 4 Carbon and Its Compounds Important Questions with Answers prepared according to the latest CBSE syllabus and NCERT guidelines. This page contains board exam oriented questions, previous year questions, short answer questions, and important concepts that help students score high marks in CBSE Class 10 Science examinations.

✓ CBSE 2025 Board Ready 14 Questions 3-Mark Format

Core Reactions

1

An organic compound 'X' is a main component of wine. When 'X' is heated with alkaline \(KMnO_{4}\), it changes into compound 'Y' which turns blue litmus red. Identify 'X' and 'Y' and write the chemical equation.

3 marks
+
Identification

Compound 'X' is Ethanol (\(CH_3CH_2OH\)) — the alcohol found in wine.
Compound 'Y' is Ethanoic Acid (\(CH_3COOH\)) — it turns blue litmus red because it is acidic.

Type of Reaction
⚗️This is an oxidation reaction. Alkaline \(KMnO_4\) acts as the oxidising agent, adding oxygen to ethanol and removing hydrogen.
Chemical Equation
\(\text{CH}_3\text{CH}_2\text{OH} \xrightarrow{\text{Alkaline KMnO}_4,\ \Delta} \text{CH}_3\text{COOH} + \text{H}_2\text{O}\)
2

Why does a candle flame look yellow and bright, while a gas stove burns with a clear blue flame? Explain the chemistry behind this difference.

3 marks
+
Gas Stove — Blue Flame

LPG (saturated hydrocarbons) + air holes → ample oxygen → complete combustion → carbon fully oxidised → clean, soot-free blue flame.

Candle — Yellow Flame

Wax vapour around the wick cannot mix quickly enough with air → incomplete combustion. Unburnt carbon particles become red-hot and glow yellow, escaping as black soot.

💡Memory tip: Blue = Complete, Yellow = Incomplete
3

Carbon is placed in Group 14. It cannot form \(C^{4+}\) cations or \(C^{4-}\) anions. Explain why it must share electrons to become stable.

3 marks
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Electronic Configuration

Carbon (atomic number 6): configuration (2, 4) → needs 4 more electrons to complete its octet.

Why not C⁴⁻?
Only 6 protons cannot hold 10 electrons — heavy electron-electron repulsion makes it energetically impossible.
Why not C⁴⁺?
🔋Removing 4 electrons successively requires an enormous amount of energy — unavailable under normal conditions.
Conclusion

Carbon shares its 4 valence electrons with other atoms to form stable covalent bonds. This is the basis of the vast organic world.

4

A student added a piece of sodium metal to a test tube containing ethanol. State two main observations and write the balanced chemical equation.

3 marks
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Observation 1

Brisk effervescence (vigorous bubbling) is seen due to rapid evolution of a colourless, odourless gas (hydrogen).

Observation 2

The gas burns with a 'pop' sound when a burning matchstick is brought near, confirming the gas is H₂. Sodium gradually dissolves.

Balanced Chemical Equation
\(2\,CH_3CH_2OH + 2\,Na \rightarrow 2\,CH_3CH_2ONa + H_2\uparrow\)
(Ethanol + Sodium → Sodium Ethoxide + Hydrogen gas)
5

What is a structural isomer? Why is it impossible to have isomers for Methane, Ethane, and Propane?

3 marks
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Definition

Structural isomers are compounds sharing the same molecular formula but with different structural arrangements of the carbon skeleton.

Why No Isomers for C₁–C₃ Alkanes?

Isomerism requires branching. 1, 2, or 3 carbon atoms can only be arranged in a single straight chain — branching is geometrically impossible with so few carbons. Isomers appear only from Butane (C₄H₁₀) onwards.

6

Vegetable oils are healthy, but vanaspati ghee is considered less healthy. Explain the chemical process used to convert oil into ghee with a chemical equation.

3 marks
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The Process — Hydrogenation

Vegetable oils contain unsaturated fatty acids (C=C double bonds). H₂ gas is added in the presence of a Nickel (Ni) catalyst at high temperature, converting double bonds to single bonds → solid saturated fat (vanaspati).

Health Aspect
🩺Unsaturated fats are easier to metabolise. Saturated fats (ghee) can raise LDL (bad) cholesterol, increasing cardiovascular risk.
Chemical Equation
\(\text{R}_2C=CR_2 + H_2 \xrightarrow{Ni,\, \Delta} \text{R}_2CH-CHR_2\)
(R = any alkyl group, e.g., –CH₃)
7

Among \(C_3H_6\), \(C_4H_{10}\), and \(C_5H_{10}\) — identify which belong to the same homologous series and give two reasons.

3 marks
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Identification

\(C_3H_6\) (Propene) and \(C_5H_{10}\) (Pentene) belong to the Alkene series.
(\(C_4H_{10}\) is Butane — an alkane, different series.)

Reason 1 — General Formula

Both fit the alkene general formula \(C_nH_{2n}\): hydrogen atoms = exactly 2× carbon atoms.

Reason 2 — Same Functional Group

Both contain a C=C double bond (unsaturation), giving them identical chemical properties and reaction types (e.g., addition reactions).

Structure & Bonding

8

Draw the electron-dot structure of Ethyne (\(C_2H_2\)). State the total number of single and triple covalent bonds.

3 marks
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Electron Sharing

Each carbon shares 3 pairs of electrons with the other carbon → triple bond. Each carbon also shares 1 pair with a hydrogen atom → single bond.

Structural Representation
H — C ≡ C — H

Each H has 2 electrons around it (duet); each C has 8 electrons (octet).

Bond Count

2 single covalent bonds (C–H bonds)
1 triple covalent bond (C≡C bond)
Total shared pairs = 5

Soap, Detergent & Saponification

9

When an ester reacts with NaOH, it breaks into two products. Name this process, state its practical use, and write the balanced equation.

3 marks
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Name of Process

Saponification — the reaction of an ester with a strong base (NaOH) to produce a soap salt and an alcohol.

Practical Use
🧼Used industrially to manufacture soap bars by hydrolyzing fats and oils with alkalis.
Chemical Equation
\(CH_3COOCH_2CH_3 + NaOH \rightarrow CH_3COONa + CH_3CH_2OH\)
(Ethyl Ethanoate + Sodium Hydroxide → Sodium Ethanoate [Soap] + Ethanol)
10

Why does hard water reduce the cleaning capacity of soap, while synthetic detergents work effectively even in hard water?

3 marks
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Soap in Hard Water

Hard water contains dissolved Ca²⁺ and Mg²⁺ ions. Soap molecules react with these ions instantly to form a sticky, insoluble white precipitate called scum — which wastes soap and stains clothes.

Detergents in Hard Water

Detergents are made from ammonium or sulphonate salts. Their charged ends do not react with Ca²⁺ or Mg²⁺ ions, so they remain soluble and produce a rich lather.

Result: Detergents clean effectively in hard water; soaps cannot.
Theory Extra — Why does soap clean at all?

Soap molecules are long chains with a hydrophilic (water-loving) head and a hydrophobic (oil-loving) tail. The tails surround grease to form tiny spheres called micelles, which are carried away by water, removing dirt.

Theory Extra — Advantage of detergents over soaps

Detergents work in hard water and even in acidic conditions, while soaps lose effectiveness. However, many synthetic detergents are non-biodegradable, causing environmental pollution — a key disadvantage.

IUPAC Naming & Structures

11

Write the IUPAC names for: (a) \(CH_3{-}CH_2{-}CH(CH_3){-}CH_2{-}OH\)   (b) \(CH_3{-}CH_2{-}C\!\equiv\!C{-}CH_3\)   (c) \(HCHO\)

3 marks
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(a)

2-Methylbutan-1-ol — longest chain = 4C (butanol); –OH at C1; –CH₃ branch at C2.

(b)

Pent-2-yne — 5-carbon chain (pent); triple bond starting at C2 from the end nearest to it.

(c)

Methanal — 1 carbon with aldehyde (–CHO) functional group.

12

Draw structural formulas showing all bonds for: (a) Propanone   (b) Butanoic Acid   (c) Bromopentane

3 marks
+
(a) Propanone (\(CH_3COCH_3\))
H O H | ‖ | H — C — C — C — H | | H H
(b) Butanoic Acid (\(CH_3CH_2CH_2COOH\))
H H H O | | | ‖ H — C — C — C — C | | | \ H H H O — H
(c) 1-Bromopentane (\(CH_3(CH_2)_3CH_2Br\))
H H H H H | | | | | H — C — C — C — C — C — Br | | | | | H H H H H

Ethanol & Ethanoic Acid

13

State two uses of Ethanol and one use of Ethanoic Acid in daily life.

3 marks
+
Uses of Ethanol

1. Industrial solvent — dissolves organic substances; used in paints, varnishes, and lacquers.
2. Medical/antiseptic use — main ingredient in hand sanitisers, cough syrups, and medical rubs.

Use of Ethanoic Acid

Food preservation (vinegar) — a 5–8% aqueous solution of ethanoic acid is vinegar, used to preserve pickles and sauces.

14

A chemist wants to make a sweet-smelling substance used in perfumes. Name the reactants, the process, and write the balanced equation.

3 marks
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Reactants & Process

Reactants: Ethanoic Acid + Ethanol. Process: Esterification. Catalyst: concentrated \(H_2SO_4\).

Chemical Equation
\(CH_3COOH + C_2H_5OH \underset{\Delta}{\xrightarrow{\text{Conc. }H_2SO_4}} CH_3COOC_2H_5 + H_2O\)
(Ethanoic Acid + Ethanol → Ethyl Ethanoate [sweet-smelling ester] + Water)

Homologous Series, Catenation & Combustion

15

Why does carbon show stronger catenation than silicon, even though both are in Group 14?

3 marks
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Bond Strength — Carbon

Carbon has a very small atomic size, so its nucleus holds shared electron pairs tightly → C–C bond is very strong and stable → long chains and rings form easily.

Silicon's Weakness

Silicon atoms are much larger → shared electrons are farther from the nucleus → Si–Si bonds are weak and break after only a few atoms.

16

Why do saturated hydrocarbons give a clean flame, while unsaturated hydrocarbons produce a smoky yellow flame in air?

3 marks
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Saturated Hydrocarbons (Alkanes)

Lower carbon-to-hydrogen ratio → enough oxygen available to completely oxidise all carbon → complete combustionclean blue flame.

Unsaturated Hydrocarbons (Alkenes/Alkynes)

Higher carbon percentage → air does not supply enough oxygen → incomplete combustion → unburnt carbon particles glow yellow, escape as black soot (smoke).

🔥This is why LPG (mainly alkanes) gives a clean blue flame on your gas stove.
17

Why can ethene undergo addition reaction with H₂, but ethane cannot? Write reaction conditions.

3 marks
+
Ethene (Unsaturated)

Contains a C=C double bond. One bond can open up to accept extra atoms → addition is possible.

Ethane (Saturated)

Contains only single bonds — all valencies are fully satisfied → no room to add atoms → addition reaction not possible.

Reaction & Conditions
\(CH_2=CH_2 + H_2 \xrightarrow{Ni/Pd,\ \Delta} CH_3-CH_3\)
(Ethene + Hydrogen → Ethane; catalyst: Ni or Pd)
18

What happens when methane reacts with chlorine in the presence of sunlight? Name the reaction type and write the equation.

3 marks
+
Reaction Type

Substitution Reaction — in the presence of sunlight, a highly reactive Cl atom replaces (substitutes) one H atom in methane.

Chemical Equation
\(CH_4 + Cl_2 \xrightarrow{\text{Sunlight}} CH_3Cl + HCl\)
(Methane + Chlorine → Chloromethane + Hydrogen Chloride)
☀️Sunlight provides the energy needed to break the Cl–Cl bond and start this chain reaction.
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