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Chapter 21 — Chapter 21 — Halogenoalkanes

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Uses and Classification of Halogenoalkanes

Source: Chemistry 12, Ch 21, 21.1

📘Easy summary

Halogenoalkanes are useful due to their chemical stability. CFCs were used as refrigerants and aerosol propellants (now being replaced by ozone-friendly alternatives). Halogenated compounds such as halothane (CF₃CHClBr) are powerful inhalation anaesthetics; chloroform was banned due to toxicity. They are intermediates for polymers such as PVC and PTFE (Teflon). A halogenoalkane forms when one or more H atoms of an alkane are replaced by halogen atoms: mono-, di-, tri- or poly-halogenoalkanes. Monohalogenoalkanes (alkyl halides, R–X) are primary (halogen-bearing carbon attached to one or no carbon: CH₃Cl, CH₃CH₂Cl, 1-chloropropane), secondary (attached to two carbons: 2-chloropropane, 2-chlorobutane) or tertiary (attached to three carbons: 2-chloro-2-methylpropane).

⭐Key points

  • R–X = alkyl halide.
  • 1°: C–X carbon bonded to ≤1 C.
  • 2°: bonded to 2 C; 3°: bonded to 3 C.
  • Uses: anaesthetics, PVC, PTFE, refrigerants.

🔬Diagram

ClassificationPrimary:CH₃CH₂ClSecondary:(CH₃)₂CHClTertiary:(CH₃)₃CClDi/tri/polyhalo: CH₂Cl₂,CHCl₃Halogenoalkanes

🌿Real-life example

(CH₃)₂CH–CH₂–Cl is 1-chloro-2-methylpropane, a primary halide.

💡Exam tip

  • Classify by counting carbons on the C–X carbon, not total carbons.

✅Quick check

1. 2-chloro-2-methylpropane is:

2. Halothane is used as:

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