An organic compound $A$ reacts with $NH_3$ on heating to give $B$. Compound $B$ reacts with $Br_2$ in the presence of $KOH$ to give $CH_3CH_2NH_2$. What is $A$?

  • A
    $CH_3COOH$
  • B
    $CH_3CH_2CH_2COOH$
  • C
    $CH_3-CH(CH_3)-COOH$
  • D
    $CH_3CH_2COOH$

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Which one of the following reaction sequences will give an azo dye?

$A$ is a neutral organic compound $(M.F.: C_8H_9ON)$. On treatment with aqueous $Br_2 / HO^{(-)}$, $A$ forms a compound $B$ which is soluble in dilute acid. $B$ on treatment with aqueous $NaNO_2 / HCl$ $(0-5^{\circ}C)$ produces a compound $C$ which on treatment with $CuCN / NaCN$ produces $D$. Hydrolysis of $D$ produces $E$ which is also obtainable from the hydrolysis of $A$. $E$ on treatment with acidified $KMnO_4$ produces $F$. $F$ contains two different types of hydrogen atoms. The structure of $A$ is

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