




The Gattermann–Koch reaction involves the formylation of aromatic compounds using carbon monoxide and hydrochloric acid in the presence of a Lewis acid catalyst, typically aluminum chloride (AlCl3). It is primarily used to introduce a formyl group (-CHO) into the benzene ring.
In the given reaction, benzene reacts with CO and HCl in the presence of AlCl3 to produce benzaldehyde. The mechanism involves the formation of an acylium ion (CHO+), which acts as an electrophile and attacks the benzene ring to form the formylated product.
Let's examine the options presented:
Therefore, the correct answer is:
The product is benzaldehyde (C6H5CHO), which matches the Gattermann–Koch reaction's expected outcome.
Consider the following sequence of reactions:
The major product $P$ is:
Which of the following are aromatic?

Give plausible explanation for:
(a) Diazonium salts of aromatic amines are stable.
(b) Aniline does not undergo Friedel-Crafts reaction.
(c) Aniline on nitration gives substantial meta product.