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OCR AS Chemistry

Revision Notes

Home / AS / Chemistry / OCR / Revision Notes / 4. Core Organic Chemistry / 4.5 Haloalkanes / 4.5.4 Environmental Concerns of Organohalogen Use


4.5.4 Environmental Concerns of Organohalogen Use


Breakdown of the Ozone Layer

Fluorohalogenoalkanes

  • The most common halogenoalkanes are chlorofluorocarbons (CFCs)
  • These compounds contain carbon atoms with chlorine and fluorine atoms attached to them
    • E.g. CCl3F and CCl2F2

  • CFCs have many uses due to their chemical inertness as they are non-flammable and non-toxic
    • They are used as refrigerators
    • Propellants for aerosols
    • As solvents for dry cleaning

Hydrofluorocarbons

  • Hydrofluorocarbons (HFCs) are compounds that contain a carbon attached to hydrogen and fluorine atoms only
    • E.g. CH2F-CF3

  • As with CFCs, HFCs are chemically inert and are therefore used for a wide range of purposes
  • Though chlorofluorocarbons (CFCs) have many beneficial uses, they also have devastating effects on the ozone layer:
    • CFCs absorb a lot of UV radiation in the upper atmosphere
    • The CFCs are then broken down by the UV light causing the formation of chlorine radicals
    • These radicals react with ozone and break down the ozone layer as shown:

Chlorine radicals and the ozone layer 

  • This is why hydrofluorocarbons (HFCs) are often used as an alternative to CFCs
  • As these compounds don’t contain any chlorine atoms, they will not have adverse effects on the ozone layer

Exam Tip

  • There is another set of accepted propagation steps for the breakdown of ozone by chlorine radicals:
    • Propagation 1: Cl• + O3 → Cl• + O2 
    • Propagation 2: ClO• + O → Cl• + O2 
  • The difference is actually in the second propagation step where this version reacts with a lone oxygen atom rather than another ozone molecule

Other radicals

  • CFCs are not the only radicals that catalyse the breakdown of the ozone
  • One of the other sets of radicals linked to ozone breakdown are the nitrogen oxide radicals which can be formed:
    • Naturally during lightning strikes
    • As a result of air travel in the stratosphere
  • Nitrogen monoxide is formed by the direct combination of nitrogen and oxygen at high temperatures inside a combustion engine
    • The nitrogen monoxide formed is a free radical as it has an odd number of electrons / unpaired electron 
  • The nitrogen monoxide radical reacts with one molecule of ozone to form the nitrogen dioxide molecule
    • NO• + O3 → NO2• + O2 
  • The nitrogen monoxide radical is then reformed 
    • NO2• + O → NO• + 2O2 
  • Overall, the breakdown equation is O3 + O → 2O2 


  • 1. Development of Practical Skills in Chemistry
    • 1.1 Physical Chemistry Practicals
      • 1.1.1 Moles Determination
        • 1.1.2 Acid-Base Titration
          • 1.1.3 Determination of Enthalpy Changes
            • 1.1.4 Reaction - Magnesium & Hydrochloric Acid
            • 1.2 Organic & Inorganic Practicals
              • 1.2.1 Qualitative Analysis of Ions
                • 1.2.2 Synthesis of a Haloalkane
                  • 1.2.3 Preparation of Cyclohexene
                    • 1.2.4 Oxidation of Ethanol
                  • 2. Foundations in Chemistry
                    • 2.1 Atoms & Reactions
                      • 2.1.1 Atomic Structure & Isotopes
                        • 2.1.2 Atomic Structure & Mass Spectrometry
                          • 2.1.3 Compounds, Formulae & Equations
                          • 2.2 Amount of Substance
                            • 2.2.1 Amount of Substance
                              • 2.2.2 Determining Formulae
                                • 2.2.3 Reaction Calculations
                                  • 2.2.4 The Ideal Gas Equation
                                    • 2.2.5 Percentage Yield & Atom Economy
                                    • 2.3 Acid-base & Redox Reactions
                                      • 2.3.1 Acids
                                        • 2.3.2 Acid-base Titrations
                                          • 2.3.3 Redox
                                          • 2.4 Electrons, Bonding & Structure
                                            • 2.4.1 Electron Structure
                                              • 2.4.2 Ionic Bonding & Structure
                                                • 2.4.3 Covalent Bonding & Structure
                                                • 2.5 The Shapes of Simple Molecules & Ions
                                                  • 2.5.1 The Shapes of Simple Molecules & Ions
                                                    • 2.5.2 Electronegativity & Bond Polarity
                                                      • 2.5.3 Intermolecular Forces
                                                    • 3. Periodic Table & Energy
                                                      • 3.1 Periodicity
                                                        • 3.1.1 Periodicity
                                                          • 3.1.2 Ionisation Energy
                                                            • 3.1.3 Structure & Physical Properties
                                                            • 3.2 Group 2
                                                              • 3.2.1 Group 2 Elements
                                                                • 3.2.2 Group 2 Compounds
                                                                • 3.3 The Halogens
                                                                  • 3.3.1 The Halogens
                                                                    • 3.3.2 Uses of Chlorine
                                                                      • 3.3.3 Qualitative Analysis
                                                                      • 3.4 Enthalpy Changes
                                                                        • 3.4.1 Enthalpy Changes
                                                                          • 3.4.2 Calorimetry
                                                                            • 3.4.3 Bond Enthalpies
                                                                              • 3.4.4 Hess' Law
                                                                              • 3.5 Reaction Rates
                                                                                • 3.5.1 Simple Collision Theory
                                                                                  • 3.5.2 Catalysis
                                                                                    • 3.5.3 The Boltzmann Distribution
                                                                                    • 3.6 Chemical Equilibrium
                                                                                      • 3.6.1 Dynamic Equilibrium
                                                                                        • 3.6.2 Le Chatelier’s Principle
                                                                                          • 3.6.3 The Equilibrium Constant, Kc
                                                                                        • 4. Core Organic Chemistry
                                                                                          • 4.1 Basic Concepts
                                                                                            • 4.1.1 Chemical Names & Formulae
                                                                                              • 4.1.2 Functional Groups
                                                                                                • 4.1.3 Structural Isomerism
                                                                                                  • 4.1.4 Reaction Mechanisms
                                                                                                  • 4.2 Alkanes
                                                                                                    • 4.2.1 Introduction to Alkanes
                                                                                                      • 4.2.2 Reactions of Alkanes
                                                                                                        • 4.2.3 Free Radical Substitution of Alkanes
                                                                                                        • 4.3 Alkenes
                                                                                                          • 4.3.1 Introduction to Alkenes
                                                                                                            • 4.3.2 Stereoisomerism in Alkenes
                                                                                                              • 4.3.3 Addition Reactions of Alkenes
                                                                                                                • 4.3.4 Electrophilic Addition
                                                                                                                  • 4.3.5 Polymers from Alkenes
                                                                                                                  • 4.4 Alcohols
                                                                                                                    • 4.4.1 Properties of Alcohols
                                                                                                                      • 4.4.2 Reactions of Alcohols
                                                                                                                      • 4.5 Haloalkanes
                                                                                                                        • 4.5.1 Reactions of Haloalkanes
                                                                                                                          • 4.5.2 Nucleophilic Substitution of Haloalkanes
                                                                                                                            • 4.5.3 Hydrolysis of Primary Haloalkanes
                                                                                                                              • 4.5.4 Environmental Concerns of Organohalogen Use
                                                                                                                              • 4.6 Organic Synthesis
                                                                                                                                • 4.6.1 Techniques
                                                                                                                                  • 4.6.2 Synthetic Routes
                                                                                                                                  • 4.7 Analytical Techniques
                                                                                                                                    • 4.7.1 Infrared Spectroscopy
                                                                                                                                      • 4.7.2 Mass Spectrometry
                                                                                                                                        • 4.7.3 Combined Techniques


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                                                                                                                                      Author: Philippa



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