Match Column-$I$ with Column-$II$ :
| Column-$I$ | Column-$II$ |
| :--- | :--- |
| $(A)$ Cyclopentanone + $2,4-$$DNP$ $\xrightarrow{\text{mild } H^+}$ Cyclopentanone$-2,4-$$DNP$ derivative | $(P)$ Electrophilic substitution |
| $(B)$ $4-$phenyl$-2-$methylbutan$-2-$ol $\xrightarrow{\text{Conc. } H_2SO_4}$ $1,1-$dimethyl$-1,2,3,4-$tetrahydronaphthalene | $(Q)$ Nucleophilic substitution |
| $(C)$ $4-$chlorocyclohexanethiol $\xrightarrow{\text{Base}}$ $7-$thiabicyclo[$2.2$.$1$]heptane | $(R)$ Nucleophilic addition |

  • A
    $A-P; B-Q; C-R$
  • B
    $A-Q; B-R; C-P$
  • C
    $A-R; B-P; C-Q$
  • D
    $A-R; B-Q; C-P$

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Match the reactant in Column-$I$ with the reaction in Column-$II$:
Column-$I$Column-$II$
$(i)$ Acetic acid$(a)$ Stephen
$(ii)$ Sodium phenate$(b)$ Friedel-Crafts
$(iii)$ Methyl cyanide$(c)$ $HVZ$
$(iv)$ Toluene$(d)$ Kolbe's

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Which of the following best describes the nucleophilic addition step in the acid-catalyzed hydrolysis of acetonitrile $(CH_3CN)$?

The conversion of $CH_{3}CH_{2}COOH$ to the product shown below can be accomplished by:
$CH_{3}CH_{2}CH(OCH_{2}CH_{2}O)$

Identify the final product in the following reaction:
$CH_3-CH(OH)-COOH \xrightarrow{\Delta} \text{Product}$

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