Show that anisole is o,p direction group towards electrophilic substitution.

Which of the following alkyl halide is more reactive towards nucleophilic substitution reaction ?

Give plausible explanation for each of the following statements: Besides the ortho and para derivatives, considerable amount of meta derivatives is also formed during nitration of aniline OR Although amino group is o - and P - directing in aromatic electrophilic substitution reactions aniline on nitration gives a substantial amount of m-nitiline

What is meant by 'leaving group' in a nucleophillic substitution reaction.

Explain the preparation of arly halides (haloarenes)using electrophilic substitution.

Aryl halides are less reactive towards nucleophilic substitution reaction than alkyl halides due to _________.

Aromatic Aldehydes and Ketones, undergo Electrophilic substitution reaction. Write the electrophils generated.

Write notes on: friedel craft's acylation.discuss the mechanism of electrophillic substitution of benzene.

Why is HNO_3 or HIO_3 added in the aromatic electrophilic substitution using iodine.

Aromatic Aldehydes and Ketones, undergo Electrophilic substitution reaction. Which position in the aromatic ring are deacivated?

Aromatic Aldehydes and Ketones, undergo Electrophilic substitution reaction. What is the major product obtained when benzaldehyde reacts with cone nitric acid?