



\(1,3-\)\(cyclohexadiene\) 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.
Let $ A \in \mathbb{R} $ be a matrix of order 3x3 such that $$ \det(A) = -4 \quad \text{and} \quad A + I = \left[ \begin{array}{ccc} 1 & 1 & 1 \\2 & 0 & 1 \\4 & 1 & 2 \end{array} \right] $$ where $ I $ is the identity matrix of order 3. If $ \det( (A + I) \cdot \text{adj}(A + I)) $ is $ 2^m $, then $ m $ is equal to:
A square loop of sides \( a = 1 \, {m} \) is held normally in front of a point charge \( q = 1 \, {C} \). The flux of the electric field through the shaded region is \( \frac{5}{p} \times \frac{1}{\varepsilon_0} \, {Nm}^2/{C} \), where the value of \( p \) is:
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