Both A and B are aromatic as they are cyclic planar and has \(4n + 2 \pi e^– (n = 1)\).
So, the correct answer is (B) : Only A and B
Given below are two statements:
Statement-I: Pure Aniline and other arylamines are usually colourless.
Statement-II: Arylamines get coloured on storage due to atmospheric reduction
In the light of the above statements, choose the most appropriate answer from the options given below:
Identify the major product formed in the following sequence of reactions:
Let \( A = \{-3, -2, -1, 0, 1, 2, 3\} \). A relation \( R \) is defined such that \( xRy \) if \( y = \max(x, 1) \). The number of elements required to make it reflexive is \( l \), the number of elements required to make it symmetric is \( m \), and the number of elements in the relation \( R \) is \( n \). Then the value of \( l + m + n \) is equal to:
For hydrogen-like species, which of the following graphs provides the most appropriate representation of \( E \) vs \( Z \) plot for a constant \( n \)?
[E : Energy of the stationary state, Z : atomic number, n = principal quantum number]
The number of 6-letter words, with or without meaning, that can be formed using the letters of the word MATHS such that any letter that appears in the word must appear at least twice, is $ 4 \_\_\_\_\_$.
The structure of Amines is shown below:
Alkylamines consist of tetrahedral nitrogen centers where the C-N-H and C-N-C bond angle is 109°. The distance between C-N bonds is smaller in comparison to the C-C range. The amines can also display a chiral property wherein the center of the nitrogen atom holds for replacements which creates solo pairs.
The bond angle in the case of trimethylamine is 108° which results in the Pyramidal structure of trimethylamine-
Due to the mixture of the solo pair with the aryl substituent, nitrogen nearly has a planar structure in aromatic amines. The C-N range is very short. In aniline, the distance between C-N bonds is similar to the distance between C-C bonds.
Read More: Structure of Amines