Know how to:
Identify functional groups
Name compounds (IUPAC)
Draw condensed and structural formulas
Functional Group | Description | Example |
---|---|---|
Alcohol (-OH) | Hydroxyl attached to a carbon | Butan-2-ol |
Carboxylic Acid (-COOH) | Carbon double bonded to O and single bonded to OH | Pentanoic acid |
Ester (-COO-) | Formed from acid + alcohol | Ethyl butanoate |
Halogenated Hydrocarbon | Hydrocarbon with Cl, Br, F, or I | 1,1,2,2-tetrachloroethane |
Pentanoic acid = carboxylic acid
Butan-2-ol = alcohol
Ethyl butanoate = ester
2-bromo-2-chloropentane = halogenated hydrocarbon
Alcohol + Carboxylic Acid → Ester + Water
Examples:
Ethanoic acid + Butan-1-ol → Butyl ethanoate + H₂O
Propanoic acid + Pentan-1-ol → Pentyl propanoate + H₂O
Important:
Use H₂SO₄ as a catalyst
Draw out full Lewis/structural diagrams when asked
Look for:
Carboxylic Acid: -COOH
Alcohol: -OH on a carbon
Halides: Cl, Br, F, I on a carbon
Benzene ring: hexagon with circle or alternating double bonds
Esters: R-COO-R'
Ethers, Aldehydes (less focus but sometimes shown)
Organic Chemistry is the study of carbon-based compounds.
Key Characteristics:
Carbon can form 4 covalent bonds
Forms chains, branched chains, and rings
Bonds with hydrogen, oxygen, nitrogen, halogens, sulfur
Hydrocarbons: compounds made only of carbon and hydrogen
Types:
Alkanes: only single bonds (saturated)
Alkenes: at least one double bond (unsaturated)
Alkynes: at least one triple bond (unsaturated)
Aromatic compounds: contain a benzene ring
Steps:
Identify the longest carbon chain (parent chain)
Number the chain to give the lowest number to the first branch or double/triple bond
Name the branches (alkyl groups) and assign numbers
Use prefixes: di-, tri-, tetra- for multiple groups
Combine name: #-branch-parent chain
Examples:
CH₄ = Methane
C₂H₆ = Ethane
CH₃CH₂CH₃ = Propane
CH₃CH=CH₂ = Propene
Prefixes (1-10 carbon atoms):
meth-, eth-, prop-, but-, pent-, hex-, hept-, oct-, non-, dec-
Functional Group | Type of Compound | Ending | Example |
---|---|---|---|
-OH | Alcohol | -ol | Ethanol |
-COOH | Carboxylic acid | -oic acid | Ethanoic acid |
-COO- | Ester | -oate | Methyl propanoate |
-Cl, -Br, -I | Halides | halo- | Chloromethane |
-NH₂ | Amine | -amine | Ethanamine |
-CHO | Aldehyde | -al | Ethanal |
-C=O (middle) | Ketone | -one | Propanone |
Condensed: CH₃CH₂CH₃
Expanded/Structural: show each bond
Line Diagrams: each line represents a bond, ends/junctions are carbon atoms
Type | Description | Example |
---|---|---|
Combustion | Reaction with O₂ to form CO₂ + H₂O | CH₄ + 2O₂ → CO₂ + 2H₂O |
Substitution | One atom replaces another | CH₄ + Cl₂ → CH₃Cl + HCl |
Addition | Double/triple bonds become single | CH₂=CH₂ + H₂ → CH₃CH₃ |
Elimination | Opposite of addition (forms double bonds) | CH₃CH₂OH → CH₂=CH₂ + H₂O |
Esterification | Alcohol + acid → ester + water | CH₃OH + CH₃COOH → CH₃COOCH₃ + H₂O |