Organic Chemistry: Deals with most compounds containing carbon.
Hydrocarbons: Compounds consisting of carbon and hydrogen only.
Examples of Organic Compounds:
Alkanes: e.g., ethane (CH3CH3)
Alkenes: e.g., ethene (CH2CH2)
Haloalkanes: e.g., chloroethane (CH3CH2Cl)
Alcohols: e.g., ethanol (CH3CH2OH)
Carboxylic Acids: e.g., ethanoic acid (CH_3COOH)
Misconceptions:
Carbon dioxide and carbonates are not considered hydrocarbons or organic compounds.
The term 'organic' in chemistry can refer to both natural and synthetic compounds.
Hydrocarbon Definition: Compound consisting of carbon and hydrogen only.
Alkane Definition: Hydrocarbon containing only single carbon-to-carbon bonds.
General formula: CnH{2n+2}
Alkene Definition: Hydrocarbon containing at least one double carbon-to-carbon bond (C=C).
General formula: CnH{2n}
Homologous Series Definition: Series of hydrocarbons with similar chemical structure and properties.
Alkanes Homologous Series: Differ by CH_2.
Methane (CH_4)
Ethane (C2H6)
Propane (C3H8)
Butane (C4H{10}
Pentane (C5H{12}
Hexane (C6H{14}
Heptane (C7H{16}
Octane (C8H{18}
*Note: Spelling of chemical names is important.
Alkenes homologous series: contains at least one C = C double bond.
Ethene (C2H4)
Propene (C3H6)
Butene (C4H8)
Pentene (C5H{10}
Hexene (C6H{12}
Heptene (C7H{14}
Octene (C8H{16}
Intramolecular Bonding: Covalent within hydrocarbon molecules.
Carbon Chain: Linear set of carbon atoms.
Intermolecular Forces (IMF): Dispersion forces are the strongest IMF in alkenes and alkanes due to their non-polar nature.
Saturated Hydrocarbons (Alkanes): Contain only single bonds between carbon atoms.
Unsaturated Hydrocarbons (Alkenes): Contain at least one carbon-to-carbon double bond.
Physical Properties: Boiling point, melting point, and viscosity are influenced by intermolecular forces (IMF).
Boiling Point Trend: Increases with the number of carbons due to increased dispersion forces.
Number of Carbons | Boiling Point (ยฐC) | State at 25ยฐC | |
---|---|---|---|
1 | -164 | gas | |
2 | -89 | gas | |
3 | -42 | gas | |
4 | -1 | gas | |
5 | 36 | liquid | |
6 | 69 | liquid | |
7 | 98 | liquid | |
8 | 125 | liquid |
Alkenes: More reactive than alkanes due to the presence of a C=C double bond (electron-rich).
Type of reactions: Addition, incomplete combustion
Enables other atoms to be added to C.
Alkanes:
Type of reactions: Substitution (in presence of UV light), combustion.
Less reactive.
Application: Fuels, starting material for synthesis of other chemicals.
Substitution Reaction: One atom or group of atoms replaces part of another molecule.
Addition Reaction: One molecule combines with another to form a larger molecule.
Hydrocarbons: Contain carbon and hydrogen.
Alkanes: Saturated hydrocarbons with single bonds between carbons.
General formula: CnH{2n+2}
Alkenes: Unsaturated hydrocarbons with at least one C=C double bond.
General formula: CnH{2n}
Homologous Series: Family of compounds that differ by CH_2.
Intermolecular Forces: Dispersion forces between adjacent molecules.
Boiling Point: Increases with carbon chain length due to stronger dispersion forces.
Chemical Properties:
Alkanes are less reactive than alkenes.
Undergo combustion and substitution reactions.
Alkenes undergo incomplete combustion and addition reactions.
Nomenclature: System developed by the International Union of Pure and Applied Chemistry (IUPAC) to name organic compounds.
Systematic Name: Standardized name used to identify organic compounds.
Examples:
CH2O2: formic acid (common name), methanoic acid (systematic name)
C2H4O_2: acetic acid (common name), ethanoic acid (systematic name)
C4H8O_2: butyric acid (common name), butanoic acid (systematic name)
C3H6O: acetone (common name), propanone (systematic name)