Elimination reactions are organic reactions where two substituents are removed from a molecule, often in the presence of acidic or basic conditions, to create unsaturated compounds. The process involves three steps: proton removal, formation of a pi bond, and breaking of the leaving group bond. There are two main types of elimination reactions: E1 (unimolecular) which involves an intermediate, and E2 (bimolecular) which occurs in a single step.