Concept:The compound
x is a primary aromatic amine because it is basic, gives carbylamine test, and forms an alkali-soluble sulfonamide.
Explanation:Molecular formula
C6H7N matches aniline (
C6H5NH2).
It is sparingly soluble in water but dissolves in dilute mineral acid due to protonation.
Carbylamine reaction with
CHCl3 and alc.
KOH gives phenyl isocyanide (
C6H5NC) with unpleasant smell, confirming a primary amine.
With benzenesulphonyl chloride, aniline forms
z,
N-phenylbenzenesulfonamide (
C6H5SO2NHC6H5), which is soluble in alkali due to acidic
NH proton.
To count different
H atoms in
z, note two monosubstituted benzene rings: one attached to
SO2 and one attached to
NH.
For the ring attached to
SO2: ortho (2
H, equivalent), meta (2
H, equivalent), para (1
H).
For the ring attached to
NH: ortho (2
H, equivalent), meta (2
H, equivalent), para (1
H).
Plus the
NH hydrogen (1
H).
Since the two rings are not symmetric, all these positions are distinct in chemical environment.
Total distinct
H atom types = 3 (from first ring) + 3 (from second ring) + 1 (
NH) = 7.
Answer:D. 7