electrophilic aromatic substitution

The reaction is an example of an electrophilic aromatic substitution.

They can also act as electrophiles in electrophilic aromatic substitution.

Electrophilic aromatic substitution takes place at C5 requiring activating groups.

Electrophilic aromatic substitution is a general method of derivatizing benzene.

In organic chemistry, this reaction is called electrophilic aromatic substitution:

The reaction is a type of electrophilic aromatic substitution accompanied by elimination of water.

Using electrophilic aromatic substitution, many functional groups are introduced onto the benzene framework.

The reaction details following the usual patterns of electrophilic aromatic substitution:

Phenol can do electrophilic aromatic substitution reactions very well.

Benzene can be easily converted to chlorobenzene by electrophilic aromatic substitution.

Pyrrole undergoes electrophilic aromatic substitution predominantly at the 2 and 5 positions.

The electrophilic aromatic substitution entering the para position was made possible by secondary cope rearrangement.

These reactions are called electrophilic aromatic substitutions.

Similarly, the Friedel-Crafts acylation is a related example of electrophilic aromatic substitution.

Ipso substitution a special case of electrophilic aromatic substitution where the leaving group is not hydrogen.

Arsabenzene undergoes electrophilic aromatic substitution at its ortho and para positions.

Like arenes, carboranes also undergo electrophilic aromatic substitution.

This reaction takes place almost exclusively in aromatic hydrocarbons, where it is called electrophilic aromatic substitution.

The presence of two activating groups also make the benzene ring highly reactive toward electrophilic aromatic substitution.

The substituents on aromatic rings affect the rate of this electrophilic aromatic substitution.

It therefore enters less readily electrophilic aromatic substitution reactions, which are characteristic of benzene derivatives.

Like benzene, naphthalene can undergo electrophilic aromatic substitution.

Electrophilic aromatic substitution at C5 requires activating groups such as a methyl group in this bromination:

The Wheland intermediate is its opposite number and the reactive intermediate in electrophilic aromatic substitution.