




Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Which of the following amine(s) show(s) positive carbamylamine test? 

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by:
Given below are two statements:
Statement I:
will undergo alkaline hydrolysis at a faster rate than 
Statement II:
In
intramolecular substitution takes place first by involving lone pair of electrons on nitrogen.
The effect of temperature on the spontaneity of reactions are represented as: Which of the following is correct?

If all the words with or without meaning made using all the letters of the word "KANPUR" are arranged as in a dictionary, then the word at 440th position in this arrangement is:
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