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Haloalkanes and Haloarenes Overview

Jul 22, 2024

Lecture Notes: Haloalkanes and Haloarenes

Introduction

*** Shivling Stars, today we are starting a one-shot video lecture on the chapter 'Haloalkanes and Haloarenes.'**

  • All students of the Winner Batch, keep up your hard work.
  • Important statement: Do not get tired, do not stop, it is still necessary to keep moving.
  • In this session, we will cover the important parts of the chapter.

Topics of Discussion

  1. Introduction to Haloalkanes and Haloarenes
  2. Classification: Categorizing into different groups
  3. Nature of C-X Bond
  4. Methods of Preparation
  5. Physical and Chemical Properties
  6. Conversion Questions

Chapter Introduction

  • Haloalkanes: - Alkanes with a halogen atom.
  • Haloarenes: - Aromatic compounds with a halogen atom.
  • General formula of Haloalkanes: R-X (R: Alkyl group, X: Halogen)

Classification

  • Haloalkanes:
    • Based on Number: Mono-, Di-, Tri-Haloalkanes
    • Hybridization Basis: SP2, SP3
  • Haloarenes: Aromatic halogens
  • Based on Branching and Stability:
    • Mono-, Di-, Tri-Haloalkanes
    • Allylic halides, Benzylic halides

Nature of C-X Bond

  • Bond Length: Increases going down the group.
  • Bond Dissociation Energy: Increases going up the group.
  • Dipole Moment: Affected by electronegativity.

Methods of Preparation

  • From Hydrocarbons:
    • Free Radical Substitution: Alkanes, Chlorination
    • Haloalkanes: Alkanes and HCl
  • From Alcohols:
    • Reaction with HX: Formation of water and halogen
    • Reaction with PCl5 and PCl3:
    • Thionyl Chloride (SOCl2): Poses Br├╕nsted reaction

Physical Properties

  • Color and Smell: Colorless in unwanted conditions, colored when halogen is present
  • State: Fewer alkanes are gases, higher alkanes are liquids, very high are solids
  • Melting and Boiling Points: Depend on various factors
    • Boiling Point: Proportional to molecular mass
    • Melting Point: Depends on symmetry

Chemical Properties

  • Nucleophilic Substitution Reactions:
    • Types: Sn1, Sn2
    • Sn2: Bimolecular, single-step reaction
    • Sn1: Unimolecular, two-step reaction
  • Elimination Reactions:
    • Proceeding via Alpha and Beta Reactions

Conversion Questions

  • Example: Aniline to Bromobenzene

Final Remarks

  • Hard work and dedication are essential.
  • Revision and Practice: Contribute more to your studies and make proper use of your time.