Formulae, Functional Groups and Terminology
Structural formula
- Definition: An unambiguous representation showing how atoms are bonded together in a molecule.
- Unlike molecular formula (which only shows the number of each atom), the structural formula shows the exact arrangement of atoms.
- Examples:
- CH₂=CH₂ → Ethene (two carbon atoms double bonded, each carbon bonded to two hydrogens)
- CH₃CH₂OH → Ethanol (two carbon atoms single bonded, first carbon bonded to three hydrogens, second bonded to two hydrogens and an –OH group)
- CH₃COOCH₃ → Methyl ethanoate (ester with a methyl group, a carbonyl, and an alkoxy group)
Displayed formula
- Shows all atoms and all bonds in a molecule.
- Every bond is represented by a line:
- Single bond = one line (–)
- Double bond = two lines (=)
- Triple bond = three lines (≡)
- Example: Ethanol:
H H | | H - C - C - O - H | | H H - Displayed formulas are important for understanding reactivity and functional groups.
General formula of homologous series
- A general formula represents the composition of a series of compounds with similar chemical properties.
- Alkanes: CₙH₂ₙ₊₂
- Example: n = 3 → C₃H₈ (propane)
- Alkenes: CₙH₂ₙ
- Example: n = 4 → C₄H₈ (butene)
- Alcohols: CₙH₂ₙ₊₁OH
- Example: n = 2 → C₂H₅OH (ethanol)
- Carboxylic acids: CₙH₂ₙ₊₁COOH
- Example: n = 3 → C₃H₇COOH (butanoic acid)
Structural isomers
- Definition: Compounds with the same molecular formula but different structural arrangements.
- Types:
- Chain isomerism – different carbon chain arrangement
- Example: C₄H₁₀:
- Butane → CH₃CH₂CH₂CH₃
- 2-Methylpropane → CH₃CH(CH₃)CH₃
- Example: C₄H₁₀:
- Position isomerism – same functional group in different positions
- Example: C₄H₈:
- But-1-ene → CH₂=CHCH₂CH₃
- But-2-ene → CH₃CH=CHCH₃
- Example: C₄H₈:
- Chain isomerism – different carbon chain arrangement
- Isomerism affects physical and sometimes chemical properties.
Functional groups
- Definition: Specific atoms or groups of atoms in a molecule that determine its chemical properties.
- Examples:
- Alkenes: C=C double bond
- Alcohols: –OH
- Carboxylic acids: –COOH
- Esters: –COO–
General characteristics of a homologous series
- Same functional group → same type of reactions.
- Same general formula → predictable formula from n.
- Differ from each other by a –CH₂– unit → difference in relative molecular mass.
- Gradual change in physical properties → e.g., boiling points increase with chain length.
- Similar chemical properties → due to identical functional group.
Saturated vs unsaturated compounds
- Saturated compound:
- All carbon–carbon bonds are single bonds.
- Examples: alkanes (C–C).
- Cannot undergo addition reactions with bromine water without UV light.
- Unsaturated compound:
- Contains at least one carbon–carbon double bond (C=C) or triple bond (C≡C).
- Examples: alkenes, alkynes.
- Undergo addition reactions easily, e.g., decolourising bromine water.
