Monday, August 4, 2025

CARBON AND ITS COMPOUNDS (CBSE 10TH NCERT CHAPTER 4 IMPORTANT KEY NOTES)

1. Covalent Bonding in Carbon

  • Carbon has 4 valence electrons → Needs 4 more to complete octet.

  • Forms covalent bonds by sharing electrons.

  • Covalent bond: Formed by sharing of electrons between atoms.

  • Common covalent compounds: Methane (CH₄), Ethane (C₂H₆), Water (H₂O), Ammonia (NH₃).

COVALENT BOND

2. Allotropes of Carbon
  • Allotropes: Different forms of the same element.

  • Diamond: Hardest, bad conductor of electricity.

  • Graphite: Soft, good conductor of electricity.

  • Fullerenes (C₆₀): Spherical molecules.

DIAMOND











GRAPHITE














FULLERENE











3. Versatile Nature of Carbon
  • Catenation: Carbon can form long chains with itself.

  • Tetravalency: Forms 4 covalent bonds → Variety of stable compounds.

  • FORMATION OF CHAINS

    Forms chains (straight, branched, rings) with single, double or triple bonds.

CATENATION
  
TETRAVALENT CARBON


4. Saturated and Unsaturated Compounds
  • Saturated hydrocarbons (Alkanes): Single bonds only → CnH₂n+₂
  • Unsaturated hydrocarbons:

    Alkenes: At least one double bond → CnH₂n
  • Alkynes: At least one triple bond → CnH₂n−₂
5. Functional Groups

  • Group of atoms that define chemical properties.

    |-------------------------
    | Alcohol | –OH | Ethanol | functional group(-OH)
    | Aldehyde | –CHO | Ethanal |functional group(-CHO)
    | Ketone | –CO– | Propanone |functional group(-CO-)
    | Carboxylic Acid | –COOH | Ethanoic acid |functional group(-COOH)
    | Halogen | –Cl, –Br, –I | Chloromethane |functional group(-Cl, -Br, -I)

6. Nomenclature of Organic Compounds
  1. Identify longest carbon chain (root word).

  2. Number the chain.

  3. Name substituents/functional group.

  4. Combine: position – substituent – parent chain – functional group.

Example: CH₃–CH₂–OH → Ethanol

7. Chemical Properties of Carbon Compounds 

Combustion

  • Hydrocarbons + O₂ → CO₂ + H₂O + heat

CH₄ + 2O₂ → CO₂ + 2H₂O

➤ Oxidation

  • Alcohols can be oxidized to acids.

CH₃CH₂OH + [O] → CH₃COOH

➤ Addition Reaction (Unsaturated)

  • Unsaturated compounds + H₂ (in presence of catalyst like Ni/Pt).

CH₂=CH₂ + H₂ → CH₃–CH₃

➤ Substitution Reaction (Saturated)

  • One hydrogen is replaced by another atom/group.

CH₄ + Cl₂ → CH₃Cl + HCl (in presence of sunlight)

8. Important Compounds

Ethanol (C₂H₅OH)

  • Liquid, soluble in water, good solvent.

  • Uses: Alcoholic drinks, antiseptic (hand sanitizer).

  • Reactions:

    • Combustion: C₂H₅OH + 3O₂ → 2CO₂ + 3H₂O

    • With acidified KMnO₄ → Acetic acid (oxidation)

Ethanoic Acid (CH₃COOH)

  • Weak acid, vinegar contains 5–8%.

  • Reactions:

    • With NaHCO₃: CH₃COOH + NaHCO₃ → CH₃COONa + CO₂ + H₂O

    • With alcohol (esterification): CH₃COOH + C₂H₅OH → CH₃COOC₂H₅ + H₂O

  • 9. Soaps and Detergents 

  • Soaps: Sodium/potassium salts of fatty acids.
  • Micelles: Soap molecules form spherical structures in water that trap grease.

  • Detergents: Synthetic, work in hard water, stronger cleaning


Important Diagrams to Practice
  • Structure of methane, ethane, ethanol.

  • Micelle formation.

  • Electron dot structure of CH₄, O₂, N₂, H₂O.

Tips for Exam
  • Understand structures and dot diagrams.

  • Practice naming (nomenclature) thoroughly.

  • Learn functional group identification.

  • Revise chemical equations – especially combustion, oxidation, substitution.

  • Solve numericals on molecular formulas and balancing equations.

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