An organic compound (A) on reduction gives compound (B) which on reaction with chloroform and potassium hydroxide forms (C). The compound (C) on catalytic reduction gives N-methyl aniline. What is the structure of compound (A)?
1. Nitrobenzene
2. Nitromethane
3. Methylamine
4. Aniline
and
are ........... isomers.
\(\mathrm {R~~~N~~~~O}\)
1.Chain
2. functional
3. position
4. all of these
An organic compound X (mol. formula C6H5O2N) has 6 carbon atoms in a ring system, three double bonds and also a nitro group as substituent X is:
1. Homocyclic but not aromatic
2. Aromatic but not homocyclic
3. Homocyclic and aromatic
4. Heterocyclic
A given nitrogen-containing aromatic compound a reacts with Sn/HCl, followed by HNO2 to give an unsatable compound B.B, on treament with phenol, forms a beautiful coloured compound C with the molecular formula C12H10N2O. The structure of compound A is