6. Understanding Organic Reactions Flashcards
A reaction in which another atom or group of atoms replaces an atom or a group of atoms. This reaction involves σ bonds: one σ bond breaks and another is formed at the same atom.
Substitution Reaction
A chemical reaction in which elements of the starting material are “lost” and a π bond is formed.
Elimination Reaction
A reaction in which elements are added to a starting material. In this reaction, a π bond is broken and two σ bonds are formed.
Addition Reaction
A detailed description of how bonds are broken and formed as a starting material is converted to a product.
Reaction Mechanism
A reaction in which all bond forming and bond breaking occurs in one step.
Concerted Reaction
A high-energy unstable intermediate formed during the conversion of a stable starting material to a stable product.
Reactive Intermediate
The breaking of a covalent bond by equally dividing the electrons between the two atoms in the bond and generates uncharged radical intermediates.
Homolysis (Homolytic Cleavage)
The breaking of a covalent bond by unequally dividing the electrons between the two atoms in the bond and generates charged intermediates.
Heterolysis (Heterloytic Cleavage)
A half-headed curved arrow used in a reaction mechanism to denote the movement of a single electron.
Fishhook
An arrow used in a reaction mechanism to denote the movement of a pair of electrons.
Full-Headed Curved Arrow
A reactive intermediate with a single unpaired electron, formed by homolysis of a covalent bond.
Radical
The energy absorbed or released in a reaction and is symbolized by ΔH°
Enthalpy Change (Heat of Reaction)
A reaction in which the energy of the products is higher than the energy of the reactants. energy is absorbed and the ΔH° is a positive value.
Endothermic
A reaction in which the energy of the products is lower than the energy of the reactants. energy is released and the ΔH° is a negative value.
Exothermic
A study of the energy and equilibrium of a chemical reaction.
Thermodynamics