Unsaturated Hydrocarbons
Compounds that contain at least one double or triple bond between carbon atoms.
Alkenes
Unsaturated hydrocarbons with at least one carbon-carbon double bond.
Alkynes
Unsaturated hydrocarbons with at least one carbon-carbon triple bond.
General Formula for Alkenes
CnH2n, where n is the number of carbon atoms.
General Formula for Alkynes
CnH2n-2, where n is the number of carbon atoms.
Nomenclature of Alkenes
Naming alkenes involves identifying the longest carbon chain containing the double bond and numbering it to give the double bond the lowest number.
Cycloalkene
A cyclic alkene where the molecule contains at least one carbon-carbon double bond.
Geometric Isomers
Compounds with the same molecular formula but different spatial arrangements of atoms due to the rigidity of double bonds.
Cis Isomer
A geometric isomer where similar groups are on the same side of a double bond.
Trans Isomer
A geometric isomer where similar groups are on opposite sides of a double bond.
Hydrogenation
A reaction where hydrogen is added across a double or triple bond, converting it to a single bond and forming an alkane.
Halogenation
An addition reaction involving the addition of halogens like Cl2 or Br2 to a double or triple bond.
Hydration
An addition reaction where water reacts with an alkene or alkyne, following Markovnikov's rule.
Hydrohalogenation
An addition reaction where hydrogen halides (HCl, HBr) are added to alkenes or alkynes.
Macromolecules
Large molecules composed of repeating structural units called monomers.
Polymers
Substances composed of long chains of repeating monomers, often used in various industrial applications.
IUPAC Naming
The systematic method of naming chemical compounds as established by the International Union of Pure and Applied Chemistry.
Substitution Reaction
A reaction in which one functional group in a compound is replaced by another.
Nitration
A chemical reaction where a nitro group (NO2) is introduced into an organic compound, typically an aromatic compound.