



\(1,3-\)\(cyclohexadiene\) is most stable because it is a neutral molecule.
All others are intermediates and hence less stable.
So, the correct option is (D).
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.
A particle is subjected to simple harmonic motions as: $ x_1 = \sqrt{7} \sin 5t \, \text{cm} $ $ x_2 = 2 \sqrt{7} \sin \left( 5t + \frac{\pi}{3} \right) \, \text{cm} $ where $ x $ is displacement and $ t $ is time in seconds. The maximum acceleration of the particle is $ x \times 10^{-2} \, \text{m/s}^2 $. The value of $ x $ is:
The molar mass of the water insoluble product formed from the fusion of chromite ore \(FeCr_2\text{O}_4\) with \(Na_2\text{CO}_3\) in presence of \(O_2\) is ....... g mol\(^{-1}\):
Given below are some nitrogen containing compounds:
Each of them is treated with HCl separately. 1.0 g of the most basic compound will consume ...... mg of HCl.
(Given Molar mass in g mol\(^{-1}\): C = 12, H = 1, O = 16, Cl = 35.5.)

Aromatic hydrocarbons, sometimes known as arenes, are aromatic organic molecules made up entirely of carbon and hydrogen. In aromatic compounds a benzene ring which is named after the simple aromatic chemical benzene, or a phenyl group when part of a larger structure, is the configuration of six carbon atoms.
Read More: Aromaticity
This reaction involves the replacement of one substituent on the ring of an aromatic hydrocarbon, commonly a hydrogen atom, by a different substituent group.
The common types of aromatic substitution reactions are:
In these types of reactions, the coupling of two fragments that have a radical nature is achieved with the help of a metal catalyst