In
electrophilic aromatic substitution reactions, existing
substituent
A substituent is one or a group of atoms that replaces (one or more) atoms, thereby becoming a moiety in the resultant (new) molecule. (In organic chemistry and biochemistry, the terms ''substituent'' and ''functional group'', as well as ''side ...
groups on the
aromatic ring influence the overall
reaction rate
The reaction rate or rate of reaction is the speed at which a chemical reaction takes place, defined as proportional to the increase in the concentration of a product per unit time and to the decrease in the concentration of a reactant per unit ...
or have a
directing effect on
positional isomer of the
products that are formed. An electron donating group (EDG) or electron releasing group (ERG, Z in structural formulas) is an atom or
functional group that donates some of its
electron density into a
conjugated π system via
resonance (mesomerism) or
inductive effects (or induction)—called +M or +I effects, respectively—thus making the π system more
nucleophilic.
As a result of these
electronic effects, an
aromatic ring to which such a group is attached is more likely to participate in
electrophilic substitution
Electrophilic substitution reactions are chemical reactions in which an electrophile displaces a functional group in a compound, which is typically, but not always, aromatic. Aromatic substitution reactions are characteristic of aromatic compounds ...
reaction. EDGs are therefore often known as activating groups, though
steric effects can interfere with the reaction.
An electron withdrawing group (EWG) will have the opposite effect on the nucleophilicity of the ring. The EWG removes electron density from a π system, making it less reactive in this type of reaction,
and therefore called deactivating groups.
EDGs and EWGs also determine the positions (relative to themselves) on the aromatic ring where substitution reactions are most likely to take place; this property is therefore important in processes of
organic synthesis
Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds. Organic molecules are often more complex than inorganic compounds, and their synthesis has developed into one o ...
.
Electron donating groups are generally
ortho/para directors for
electrophilic aromatic substitutions, while electron withdrawing groups are generally
meta directors with the exception of the
halogen
The halogens () are a group in the periodic table consisting of five or six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), astatine (At), and tennessine (Ts). In the modern IUPAC nomenclature, this group is ...
s which are also ''ortho''/''para'' directors as they have
lone pair
In chemistry, a lone pair refers to a pair of valence electrons that are not shared with another atom in a covalent bondIUPAC ''Gold Book'' definition''lone (electron) pair''/ref> and is sometimes called an unshared pair or non-bonding pair. Lone ...
s of electrons that are shared with the aromatic ring.
Categories

Electron donating groups are typically divided into three levels of activating ability (The "extreme" category can be seen as "strong".) Electron withdrawing groups are assigned to similar groupings. Activating substituents favour electrophilic substitution about the ''ortho'' and ''para'' positions.