$C_6H_5NHCH_3$ is:
Strongest base in aqueous medium:
Gabriel phthalimide synthesis gives:
Carbylamine test reagent:
Diazotization is done at:
Aniline is less basic than methylamine because:
Hinsberg test for $2°$ amine:
Anilinium sulfate is:
p-Nitroaniline basicity vs aniline:
Coupling of $ArN_2^+$ with $C_6H_5OH$ gives:
Number of H's on N in primary amine:
Number of H's on N in $(CH_3)_3N$:
Number of $1°$ amines from Gabriel synthesis (with one alkyl halide):
Assertion (A): Aniline gives carbylamine reaction. Reason (R): Aniline is a primary amine; with CHCl₃/KOH it forms phenyl isocyanide.
Assertion (A): Diazonium salts are useful synthetic intermediates. Reason (R): They can be converted to a wide range of aromatic compounds (ArCl, ArBr, ArI, ArOH, ArCN, ArF, ArH, ArNO₂, ArAr) by various reactions.
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