The incorrect match is:

  • A
    The structure of $2$-acetoxybenzoic acid : $\text{Aspirin}$
  • B
    $Cl_3C-CH(C_6H_4Cl)_2$ : $\text{D.D.T.}$
  • C
    $H_2N-CO-NH_2$ : $\text{Urea}$
  • D
    $H_2N-C_6H_4-SO_3H$ : $\text{Sulphanilic acid}$

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Similar Questions

$CH_3-CO-CH_2-CH_2-CH_2-CO_2H \xrightarrow[(ii) H_2O, H^+]{(i) NaBH_4} ?$
What will be the final product of this transformation?

In the following sequence of reactions,a compound $A$ (molecular formula $C_{6}H_{12}O_{2}$) with a straight chain structure gives a $C_{4}$ carboxylic acid. $A$ is :
$A$ $\xrightarrow{LiAlH_{4} / H_{3}O^{+}} B$ $\xrightarrow{\text{Oxidation}} C_{4} \text{ carboxylic acid}$

Match the reactions given in Column-$I$ with their products in Column-$II$.
Column-$I$ (Reactant) Column-$II$ (Product)
$A$. $RCH_2OH \xrightarrow[(ii) H_3O^{+}]{(i) NaOH, KMnO_4} ?$ $i$. $C_6H_5COOH + C_2H_5OH$
$B$. $CH_3(CH_2)_8CH_2OH \xrightarrow{Jones reagent} ?$ $ii$. $RCOOH$
$C$. $RCONH_2 \xrightarrow{H_3O^{+}, \Delta} ?$ $iii$. $CH_3(CH_2)_8COOH$
$D$. $C_6H_5COOEt \xrightarrow{H_3O^{+}} ?$ $iv$. $RCOOH + NH_3$

Difficult
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Which $\beta$-keto acid shown will not undergo decarboxylation?

The correct order of acid strength of the following carboxylic acids is $-$

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