Electrolytic reduction of nitrobenzene in weakly acidic medium gives
A
Aniline
B
Nitrosobenzene
C$N-$Phenylhydroxylamine
D$p-$Hydroxylaniline
AIPMT 2005, Medium
Download our app for free and get started
A
Aniline
a (a)
Download our app
and get started for free
Experience the future of education. Simply download our apps or reach out to us for more information. Let's shape the future of learning together!No signup needed.*
The decreasing order of reactivity of $m-$ nitrobromobenzene $(I), 2, 4, 6-$ trinitrobromo-benzene $(II), p-$ nitrobromobenzene $(III)$, and $2,4-$ dinitrobromobenzene $(IV),$ towards $OH^-$ ions is
$1.86\, g$ of aniline completely reacts to form acetanilide. $10 \,\%$ of the product is lost during purification. Amount of acetanilide obtained after purification (in $g$) is ...... $\times 10^{-2}.$