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4.1.2Core Organic Chemistry

Functional Groups

5 min read 5 parts Lesson 3 of 29

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Section 1 of 5What a Functional Group Does

4.1.2 Functional Groups

Knowing the group tells you which reactions to expect and how to name the compound.

Definition
  • A functional group is the atom or group of atoms in a molecule that is responsible for its characteristic reactions.
Same series
  • Compounds with the same group form a homologous series with similar chemical properties and a gradual change in physical properties.
Saturated
  • A saturated compound contains only single carbon-carbon bonds, as in alkanes.
Unsaturated
  • An unsaturated compound contains at least one carbon-carbon double or triple bond, as in alkenes.

Section 2 of 5Common Groups and Their Naming

Common Groups and Their Naming
Alkene
  • The C=C group is named with the suffix -ene, as in propene.
Alcohol
  • The –OH group gives the suffix -ol, or the prefix hydroxy- when a higher priority group is present.
Carbonyl
  • Aldehydes (–CHO, suffix -al) and ketones (C=O in the chain, suffix -one) both contain the C=O bond.
Carboxylic acid
  • The –COOH group has the suffix -oic acid, as in ethanoic acid.
Haloalkane
  • Halogen atoms are named with the prefixes fluoro-, chloro-, bromo- and iodo-, as in 1-bromopropane.
GroupFormulaExample
Alcohol–OHEthanol, CH₃CH₂OH
Aldehyde–CHOEthanal, CH₃CHO
KetoneC=OPropanone, CH₃COCH₃
Carboxylic acid–COOHEthanoic acid, CH₃COOH
Ester–COO–Methyl ethanoate, CH₃COOCH₃
Amine–NH₂Ethylamine, CH₃CH₂NH₂

Section 3 of 5Choosing the Name

1
Identify every functional group present in the molecule from the displayed or structural formula.
2
Decide which group has priority; a carboxylic acid outranks an aldehyde, which outranks a ketone and then an alcohol.
3
Use the highest priority group as the suffix, and name the other groups as prefixes.
4
Number the main chain so the suffix group has the lowest possible number.
5
State the position of every prefix and check that the name matches the structure.

Section 4 of 5Linking Group to Properties

Polarity
  • Groups containing oxygen or nitrogen make molecules polar and able to form stronger intermolecular forces.
Hydrogen bonding
  • Alcohols and carboxylic acids can form hydrogen bonds, which raises boiling points and gives solubility in water.
Reactivity
  • Alkenes react by addition at the C=C bond, whereas haloalkanes react at the polar carbon-halogen bond.
Acidity
  • Carboxylic acids release H⁺ ions in water, so they behave as weak acids.

Section 5 of 5Exam Checklist & Tips

4.1.2 – Key Points for the Exam

  • Functional group The atom or group of atoms that determines the characteristic reactions of a compound.
  • Saturated Containing only single bonds between carbon atoms.
  • Unsaturated Containing at least one C=C or C≡C bond.
  • Ester A compound containing the –COO– group formed from a carboxylic acid and an alcohol.

Common Mistakes

  • Confusing aldehydes and ketonesthe aldehyde C=O is at the end of the chain, a ketone C=O is within the chain.
  • Writing an ester group in the wrong order and so naming the alcohol and acid parts the wrong way round.
  • Forgetting that the suffix is chosen by group priority and not by the first group seen.
  • Writing an alcohol as –COH, which wrongly suggests an aldehyde.
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