$A$ $\xrightarrow[\text{(ii) } H_3O^{+}]{\text{(i) } NaOH} B$ $\xrightarrow[\text{(ii) } H_2SO_4, \Delta]{\text{(i) } EtOH} C$
'$A$' shows positive Lassaigne's test for $N$ and its molar mass is $121$.
'$B$' gives effervescence with aq. $NaHCO_3$.
'$C$' gives fruity smell.
Identify $A, B$ and $C$ from the following.

  • A
    $A$ = Benzamide,$B$ = Benzoic acid,$C$ = Ethyl benzoate
  • B
    $A$ = Benzylhydrazine,$B$ = Benzoic acid,$C$ = Ethyl benzoate
  • C
    $A$ = p-Aminobenzaldehyde,$B$ = p-Aminomandelic acid,$C$ = p-Aminomandelic acid ethyl ester
  • D
    $A$ = Anthranilaldehyde,$B$ = Anthranilic acid,$C$ = Ethyl anthranilate

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Similar Questions

An ester $(A)$ with molecular formula $C_9H_{10}O_2$ is reacted with an excess of $CH_3MgBr$. The resulting product is treated with concentrated $H_2SO_4$ to form an olefin $(B)$. Ozonolysis of $(B)$ yields a ketone with the formula $C_8H_8O$. What is the structure of $(A)$?

Match Column-$I$ with Column-$II$ based on the $pK_a$ values of the given carboxylic acids:
Column-$I$Column-$II$
$(A)$ $CF_3COOH$$(i)$ $3.41$
$(B)$ Benzoic acid$(ii)$ $4.76$
$(C)$ $CH_3COOH$$(iii)$ $0.23$
$(D)$ $4$-nitrobenzoic acid$(iv)$ $4.20$

The final product $(III)$ obtained in the reaction sequence is:
$CH_3-CH_2-COOH$ $\xrightarrow{PCl_3} I$ $\xrightarrow{C_6H_6/AlCl_3} II$ $\xrightarrow{NH_2-NH_2/\text{base/heat}} III$

Assertion : The $pK_a$ of acetic acid is lower than that of phenol.
Reason : Phenoxide ion is more resonance stabilised.

What are the products formed at the anode during Kolbe synthesis?

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