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OCR AS Chemistry

Revision Notes

Home / AS / Chemistry / OCR / Revision Notes / 4. Core Organic Chemistry / 4.1 Basic Concepts / 4.1.2 Functional Groups


4.1.2 Functional Groups


Homologous Series

  • Organic chemistry is the chemistry of carbon compounds
  • Carbon forms a vast number of compounds because it can form strong covalent bonds with itself
  • This enables it to form long chains of carbon atoms, and hence an almost infinite variety of carbon compounds are known

Catenation in Carbon, downloadable IB Chemistry revision notes

An almost infinite variety of chains, branches and rings is possible 

Homologous series

  • A homologous series is a group of organic compounds that have the same functional group, but each successive member differs by CH2

An Introduction to AS Level Organic Chemistry Ethanol and Propanol, downloadable AS & A Level Chemistry revision notes

Ethanol and propanol belong to the same homologous series

Homologous Series of Alkanes

  • Things we can say about a homologous series:
    • Each member has the same functional group
    • Each member has the same general formula
    • Each member has similar chemical properties
    • Each successive member differs by  -CH2 –
    • Members have gradually changing physical properties, for example, boiling point, melting point and density

  • As a homologous series is ascended, the size of the molecule increases
  • This has an effect on the physical properties, such as boiling point and density

Describing Chemicals

  • A functional group is a group of atoms that are responsible for the characteristic reactions of a compound
    • They determine the physical and chemical properties of molecules
  • Organic compounds can be classified into one of three categories:
    1. Aliphatic - a compound containing carbon and hydrogen joined together in straight chains, branched chains or non-aromatic rings
    2. Alicyclic - this is an aliphatic compound arranged in non-aromatic rings with or without side chains
    3. Aromatic - a compound containing a benzene ring
  • The table below shows a summary of common functional groups found in compounds
  • R is any other atom or group of atoms (except for hydrogen)

Functional Groups found in Compounds Table

An Introduction to AS Level Organic Chemistry Functional Groups, downloadable AS & A Level Chemistry revision notes

Exam Tip

Remember: Organic compounds can also be described as:
  • Saturated - containing single carbon–carbon bonds only
  • Unsaturated - containing a minimum of one carbon-carbon bond that is not single, e.g. C=C or C≡C

Converting Names to Formulae

  • As previously discussed, a homologous series is a group of organic compounds that have the same functional group, but each successive member differs by CH2 
    • The homologous series of hydrocarbons called the alkanes has the general formula CnH2n+2 
    • The homologous series of hydrocarbons called the alkenes has the general formula CnH2n 
  • These general formulae can be used to predict the chemical formula of any member of the same homologous series

Worked Example

Use the descriptions to deduce the formula of the following chemicals:
  1. Eicosane - an alkane containing a 20 carbon backbone
  2. n-nonapentacontane - a long chain alkane isolated in 1997 containing 59 carbons
  3. Oct-3-ene - an 8 carbon alkene with one C=C bond on carbon-3 

Answers

Answer 1: Eicosane is an alkane so has the general formula CnH2n+2 
There are 20 carbons so n is 20, which means that there are 2n+2 hydrogens or (2 x 20) + 2 = 42
Therefore, the formula of eicosane is C20H42 

Answer 2: n-nonapentacontane is an alkane so has the general formula CnH2n+2 
There are 59 carbons so n is 59, which means that there are 2n+2 hydrogens or (2 x 59) + 2 = 120
Therefore, the formula of n-nonapentacontane is C59H120 

Answer 3: Oct-3-ene is an alkene so has the general formula CnH2n
There are 8 carbons in oct-3-ene so n is 8, which means that there are 2n hydrogens or (2 x 8) = 16
Therefore, the formula of oct-3-ene is C8H16 

  • The process shown in the worked examples can be applied to any homologous series providing that the general formula and the number of at least one of the component elements are known


  • 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: Richard

                                                                                                                                      Richard has taught Chemistry for over 15 years as well as working as a science tutor, examiner, content creator and author. He wasn’t the greatest at exams and only discovered how to revise in his final year at university. That knowledge made him want to help students learn how to revise, challenge them to think about what they actually know and hopefully succeed; so here he is, happily, at SME.


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