An isocyanide on hydrolysis gives

  • A
    An amide
  • B
    $A$ carboxylic acid and ammonia
  • C
    $A$ $N$-substituted amide
  • D
    $A$ $1^o$-amine and formic acid

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With which of the following compounds does aniline react to form a Schiff base?

Identify the products $y$ and $x$ in the following reaction sequence:
$C_6H_5CONH_2 \xrightarrow{NaOBr} y$
$C_6H_5CONH_2 \xrightarrow[(ii) H_3O^+]{(i) C_6H_5SO_2Cl / py, \Delta} x$

$A$ compound $X$ on treatment with $Br_2/NaOH$ provided $C_3H_9N$,which gives a positive carbylamine test. Compound $X$ is

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Assertion : Anilinium chloride is more acidic than ammonium chloride.
Reason : Anilinium ion is resonance stabilized.

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