Hydrocarbons: The Energy Heroes ⛽

Hydrocarbons = Carbon + Hydrogen only! They’re everywhere in daily life:

  • 🔥 Fuels: LPG (Liquified Petroleum Gas), CNG (Compressed Natural Gas), petrol, diesel, kerosene
  • ♻️ Less pollution: LPG & CNG are cleaner options
  • 🏭 Industrial uses: Make plastics (polythene, polypropene), paints, dyes, medicines

Why Study Hydrocarbons? 🎯

By the end of this unit, you’ll be able to:

  • Name hydrocarbons using IUPAC rules
  • Draw structures & isomers (same formula, different arrangement)
  • Prepare hydrocarbons in the lab
  • Tell apart alkanes, alkenes, alkynes & aromatics using properties
  • Understand benzene’s special “aromaticity” ✨

Classification of Hydrocarbons 🧩

Based on carbon-carbon bonds:

TypeBonds PresentExamples
SaturatedOnly C-C & C-H single bonds Alkanes (open chain)
Cycloalkanes (closed chain)
UnsaturatedC-C double/triple bonds 😮Alkenes (C=C), Alkynes (C≡C)
AromaticSpecial ring structures ⭕Benzene

Alkanes: The Simple Ones 😇

  • Formula: \( \ce{C_nH_{2n+2}} \)
  • Inert: Don’t react easily (old name: paraffins = low affinity)
  • Start with Methane (\(\ce{CH4}\)) → replace H with \(-\ce{CH3}\) → get next alkane!

Methane’s Structure 🔺

  • Tetrahedral shape (like a pyramid)
  • Bond angle: 109.5°
  • Bond lengths: C-H = 112 pm, C-C = 154 pm
  • Bonds form by head-on overlap of carbon’s \(sp^3\) orbitals + hydrogen’s 1s orbital

Structure of Methane

H
|
H-C-H
|
H

Naming & Isomers 🤔

  • First 3 alkanes (methane/ethane/propane) have only one structure.
  • Butane (\(\ce{C4H10}\)) has 2 isomers:
    1. n-Butane: Straight chain ⛓️ (Boiling point: 273 K)
    2. Isobutane: Branched chain 🌿

n-Butane

H   H   H   H
|   |   |   |
H-C-C-C-C-H
|   |   |   |
H   H   H   H

NEET Must-Knows! 💡

  1. Classification: Saturated vs. unsaturated vs. aromatic hydrocarbons.
  2. Alkane general formula: \( \ce{C_nH_{2n+2}} \) and isomerism (e.g., butane’s 2 structures).
  3. Methane structure: Tetrahedral, bond angle 109.5°, bond lengths (C-H=112pm, C-C=154pm).
  4. Bonding in alkanes: Formed by head-on overlap of \(sp^3\) orbitals (carbon) + 1s orbitals (hydrogen).