Functional Group | Name Example | Structure or Notes |
---|---|---|
Carboxylic Acid | ethanoic acid | –COOH |
Alcohol | butan-2-ol, hexan-3-ol | –OH |
Ester | ethyl butanoate | –COO– |
Halogenated Hydrocarbon | 1,5-dichlorohexane | Contains halogens like Cl, Br, F, I |
Ether (FYI only) | (e.g., in vanilla) | –O– (Not tested but appears in visuals) |
Aldehyde (FYI only) | (e.g., in vanilla) | –CHO (You don’t need to memorize it) |
Find the longest carbon chain.
Number to give functional group the lowest number.
Name substituents and functional groups.
Use prefixes: di-, tri- if multiple halogens or groups.
Acid + Alcohol → Ester + Water
Catalyst: H₂SO₄ (sulfuric acid)
Example: Ethanoic acid + butan-1-ol → butyl ethanoate + H₂O
Acids | Bases |
---|---|
Sour taste | Bitter taste |
pH < 7 | pH > 7 |
Turns blue litmus red | Turns red litmus blue |
Conducts electricity (electrolyte) | Also conductive if strong |
Arrhenius Acid: Produces H⁺ in solution
Arrhenius Base: Produces OH⁻ in solution
Brønsted-Lowry Acid: Proton (H⁺) donor
Brønsted-Lowry Base: Proton (H⁺) acceptor
Scale: 0–14
<7 = Acidic, 7 = Neutral, >7 = Basic
Strong acids/bases: Fully dissociate in water
Weak acids/bases: Partially dissociate
pH = -log[H⁺]
Concentration affects pH
Strength affects degree of dissociation, not just pH
Fuel (hydrocarbon) + O₂ → CO₂ + H₂O
Incomplete combustion → CO or C (soot)
SO₂, NO₂ released → Combine with H₂O → acids
SO₂ + H₂O → H₂SO₃ (sulfurous acid)
SO₃ + H₂O → H₂SO₄ (sulfuric acid)
NO₂ + H₂O → HNO₂ and HNO₃
Jet Stream: Spreads acid rain
Limestone Buffer: Neutralizes acid
Metal Leaching: Acids dissolve toxic metals into water
Plant nutrients: Washed away or uptake blocked
Scrubbers: Remove SO₂ from exhaust gases
Catalytic Converters: Reduce NOx emissions
Photochemical Smog: Controlled via alternative transportation & reducing emissions
ethanoic acid + butan-1-ol → butyl ethanoate + H₂O
pentan-1-ol + propanoic acid → pentyl propanoate + H₂O
Look for:
–OH = alcohol
–COOH = carboxylic acid
–Cl, –Br, –F = halogenated hydrocarbon
Benzene ring = aromatic compound