Class 12Chemistry2 Aldehydes, Ketones and Carboxylic Acids: Carboxylic Acids and their DerivativesMix Examples-Carboxylic acids and Their derivative
MediumMatch 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 |
| 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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Similar Questions
Amongst the following, the total number of compounds soluble in aqueous $NaOH$ at room temperature is:
$(I)$ Benzaldehyde
$(II)$ $1$-Naphthol
$(III)$ $4$-(Dimethylamino)phenol
$(IV)$ $4$-Methylphenol
$(V)$ Benzoic acid
$(VI)$ $N,N$-Dimethylcyclohexanamine
$(VII)$ $1$-Naphthoic acid
$(VIII)$ $1,4$-Di-tert-butylbenzene
$(IX)$ $1$-Naphthylmethanol
$(I)$ Benzaldehyde
$(II)$ $1$-Naphthol
$(III)$ $4$-(Dimethylamino)phenol
$(IV)$ $4$-Methylphenol
$(V)$ Benzoic acid
$(VI)$ $N,N$-Dimethylcyclohexanamine
$(VII)$ $1$-Naphthoic acid
$(VIII)$ $1,4$-Di-tert-butylbenzene
$(IX)$ $1$-Naphthylmethanol
DifficultJEE MAIN 2026
View SolutionMatch the formulas in Column-$I$ with their names in Column-$II$.
Column-$I$ (formula)
Column-$II$ (name)
$A$. $RCH=NH$
$i$. Diisobutyl aluminium hydride
$B$. $AlH(i-Bu)_2$
$ii$. Benzalchloride
$C$. $C_6H_5-CH(OCOCH_3)_2$
$iii$. Imine
$D$. $C_6H_5CHCl_2$
$iv$. Benzylidene diacetate
| Column-$I$ (formula) | Column-$II$ (name) |
| $A$. $RCH=NH$ | $i$. Diisobutyl aluminium hydride |
| $B$. $AlH(i-Bu)_2$ | $ii$. Benzalchloride |
| $C$. $C_6H_5-CH(OCOCH_3)_2$ | $iii$. Imine |
| $D$. $C_6H_5CHCl_2$ | $iv$. Benzylidene diacetate |
Medium
View Solution$CH_3-CH_2-CH=O$ $\xrightarrow[(2) H^{+}]{(1) \text{Tollen's reagent}} X$ $\xrightarrow[(2) \text{dry distillation}]{(1) Ca(OH)_2} Y$; $Y$ is
Difficult
View SolutionHydrolysis of an ester gives a carboxylic acid,which upon Kolbe's electrolysis yields ethane. Identify the ester.
Medium
View SolutionWhat are $\underline{A}, \underline{B}, \underline{C}$ in the following reactions?
$(I)$ $(CH_3 CO_2)_2 Ca \stackrel{\Delta}{\longrightarrow} \underline{A}$
$(II)$ $CH_3 CO_2 H \underset{\text{Red P}}{\stackrel{HI}{\longrightarrow}} \underline{B}$
$(III)$ $2 CH_3 CO_2 H \stackrel{P_4 O_{10}}{\longrightarrow} \underline{C}$
$\underline{A} \quad \underline{B} \quad \underline{C}$
$(I)$ $(CH_3 CO_2)_2 Ca \stackrel{\Delta}{\longrightarrow} \underline{A}$
$(II)$ $CH_3 CO_2 H \underset{\text{Red P}}{\stackrel{HI}{\longrightarrow}} \underline{B}$
$(III)$ $2 CH_3 CO_2 H \stackrel{P_4 O_{10}}{\longrightarrow} \underline{C}$
$\underline{A} \quad \underline{B} \quad \underline{C}$
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