Class 10 Science Chapter 4 Carbon and its Compounds Short Notes

A quick revision summary for right before the exam: every definition, equation and named fact from the chapter, all in one place. The full notes are available separately for detailed reading.

1 Covalent Bonding and Allotropes

  • Covalent bond: formed by sharing a pair of electrons between two atoms, so both get a full outer shell
  • H₂: single bond · O₂: double bond · N₂: triple bond · CH₄: carbon (tetravalent) shares with 4 H atoms
  • Carbon does not readily form C⁴⁺ or C⁴⁻ ions: both need too much energy or leave an unstable ion
  • Diamond: 4 bonds/carbon, rigid 3-D network, hardest substance known, does not conduct
  • Graphite: 3 bonds/carbon (one is a double bond, so valency is satisfied), hexagonal layers, soft and slippery, conducts electricity
  • Fullerene: C-60, football-shaped, named after architect Buckminster Fuller

2 Why Carbon Forms So Many Compounds

1. Catenation
Carbon’s unique ability to bond with other carbon atoms, forming chains, branches or rings. Silicon manages only 7-8 atoms; carbon’s chains are far longer and stable.
2. Tetravalency
Carbon’s valency of 4: it bonds to 4 other atoms (carbon or another element). Small size lets carbon’s nucleus hold shared electrons strongly, giving strong bonds.

1828: Friedrich Wöhler prepared urea from ammonium cyanate, disproving the “vital force” theory that carbon compounds needed a living system to form.

3 Classifying Carbon Compounds

C atoms Name Formula
1 Methane CH₄
2 Ethane C₂H₆
3 Propane C₃H₈
4 Butane C₄H₁₀
5 Pentane C₅H₁₂
6 Hexane C₆H₁₄
3. Saturated / unsaturated
Saturated: only single C-C bonds (alkanes), less reactive. Unsaturated: a double (alkenes) or triple (alkynes) C-C bond, more reactive.
4. Structural isomers
Same molecular formula, different structure, e.g. butane’s straight-chain and branched forms.

Functional groups: -Cl/-Br haloalkane · -OH alcohol · -CHO aldehyde · -CO- ketone · -COOH carboxylic acid.
Homologous series: same functional group, successive members differ by -CH₂- (14 u). Alkene formula: CnH2nC_nH_{2n}.
Naming: count carbons → base name; add prefix/suffix for the functional group; drop final “e” before a vowel suffix (propan + one = propanone); unsaturation changes “ane” to “ene”/”yne”.

4 Reactions of Carbon Compounds

C+OX2→COX2↑+heat and light\ce{C + O2 -> CO2 ^ + heat and light}
CHX4+2 OX2→COX2+2 HX2O+heat and light\ce{CH4 + 2O2 -> CO2 + 2H2O + heat and light}
CHX4+ClX2→sunlightCHX3Cl+HCl\ce{CH4 + Cl2 ->[\text{sunlight}] CH3Cl + HCl} (substitution)

  • Combustion: saturated → clean flame; unsaturated/limited air → yellow, sooty flame; coal/petroleum’s N and S give polluting oxides
  • Oxidation: alkaline KMnO₄ or acidified K₂Cr₂O₇ (oxidising agents) turn alcohols into acids
  • Addition: unsaturated + H₂, with Pd/Ni catalyst → saturated (e.g. hydrogenating vegetable oil)
  • Substitution: chlorine replaces hydrogen one by one, in sunlight

5 Ethanol and Ethanoic Acid

Ethanol Ethanoic acid
Litmus Neutral Turns blue red
MP / BP 156 K / 351 K 290 K (glacial acetic acid)
With Na H₂ gas + sodium ethoxide H₂ gas + sodium ethanoate
With NaHCO₃ No reaction Brisk fizz, CO₂ gas

2 Na+2 CHX3CHX2OH→2 CHX3CHX2OX− NaX++HX2↑\ce{2Na + 2CH3CH2OH -> 2CH3CH2O- Na+ + H2 ^}
CHX3−CHX2OH→443 Kconc.  HX2SOX4CHX2=CHX2+HX2O\ce{CH3-CH2OH ->[\text{conc. } H2SO4][443\ K] CH2=CH2 + H2O} (dehydration)
CHX3COOH+CHX3CHX2OH→acid catalystCHX3COOCX2HX5+HX2O\ce{CH3COOH + CH3CH2OH ->[\text{acid catalyst}] CH3COOC2H5 + H2O} (esterification)
CHX3COOCX2HX5+NaOH→CX2HX5OH+CHX3COONa\ce{CH3COOC2H5 + NaOH -> C2H5OH + CH3COONa} (saponification)
CHX3COOH+NaHCOX3→CHX3COONa+HX2O+COX2↑\ce{CH3COOH + NaHCO3 -> CH3COONa + H2O + CO2 ^}

Vinegar: 5-8% ethanoic acid in water. Methanol: oxidised to methanal in the liver; can cause blindness or death. Denatured alcohol: ethanol + methanol (poison) + blue dye.

6 Soaps and Detergents

5. Micelle
A cluster of soap molecules in water, hydrophobic (hydrocarbon) tails pointing into an oil droplet, hydrophilic (ionic) heads facing outward into the water.
  • Soap = sodium/potassium salt of a long-chain carboxylic acid
  • Hard water (Ca²⁺/Mg²⁺) + soap → insoluble curdy scum, poor lather
  • Detergents (sulphonate/ammonium salts) do not form this precipitate → work well in hard water
  • Micelles stay suspended as a colloid (ion-ion repulsion) and scatter light, so soap solution looks cloudy
Fastest possible revision
  • Covalent bond = shared electron pair. Diamond: 4 bonds/C, hard, insulator. Graphite: 3 bonds/C, soft, conducts. Fullerene: C-60, football shape
  • Catenation + tetravalency = millions of carbon compounds
  • Saturated (alkanes, single bonds) vs unsaturated (alkenes double, alkynes triple)
  • Homologous series: same functional group, +14 u per member
  • Ethanol: neutral, reacts with Na, dehydrates to ethene at 443 K
  • Ethanoic acid: weak acid, vinegar, glacial (290 K), reacts with base and carbonates giving CO₂
  • Soap cleans via micelles; fails in hard water (scum); detergents don’t