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:
List I (Spectral Lines of Hydrogen for transitions from) | List II (Wavelength (nm)) | ||
A. | n2 = 3 to n1 = 2 | I. | 410.2 |
B. | n2 = 4 to n1 = 2 | II. | 434.1 |
C. | n2 = 5 to n1 = 2 | III. | 656.3 |
D. | n2 = 6 to n1 = 2 | IV. | 486.1 |
The following diagram shown restriction sites in E. coli cloning vector pBR322. Find the role of ‘X’ and ‘Y’gens :
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