(A) Step $1$: The reaction of Grignard reagent $C_2H_5MgBr$ with $ClCN$ gives $C_2H_5CN$. Acidic hydrolysis of $C_2H_5CN$ yields propanoic acid,$C_2H_

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(A) Step $1$: The reaction of Grignard reagent $C_2H_5MgBr$ with $ClCN$ gives $C_2H_5CN$. Acidic hydrolysis of $C_2H_5CN$ yields propanoic acid,$C_2H_5COOH$. Thus,$B = C_2H_5COOH$.Step $2$: The reaction of acetone $(CH_3COCH_3)$ with $I_2$ and $NaOH$ is the iodoform test. It produces sodium acetate $(CH_3COONa)$ and iodoform $(CHI_3)$. Thus,$X = CH_3COONa$.

Class 12 Chemistry 8-2.Carboxylic acids and Their derivative Mix Examples-Carboxylic acids and Their derivative

Medium

In the following reactions,what are $B$ and $X$ respectively?
$C_2H_5MgBr$ $\xrightarrow{ClCN} C_2H_5CN$ $\xrightarrow{H_3O^+} B$
$CH_3COCH_3$ $\xrightarrow[NaOH]{I_2} X + CHI_3$ $\xrightarrow{Ag} Y$
$C_6H_5NH_2$ $\xrightarrow[HCl]{NaNO_2} P$ $\xrightarrow{CuCN} Q$ $\xrightarrow{+4H} R$

A
$C_2H_5COOH, CH_3COONa$
B
$C_2H_5COOH, CH_3I$
C
$C_2H_5CH_2NH_2, CH_3I$
D
$C_2H_5COOH, CH_3COONa$

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8-2.Carboxylic acids and Their derivative

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Mix Examples-Carboxylic acids and Their derivative

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

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$CH_3-CO-CH_2-COOC_2H_5 \xrightarrow{NaOH, H_2O} A$. The product '$A$' in the reaction is

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In the given reaction $[X]$ will be :

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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 :
$A$ $\xrightarrow{LiAlH_{4} / H_{3}O^{+}} B$ $\xrightarrow{\text{Oxidation}} C_{4} \text{ carboxylic acid}$

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

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In the following reactions,what are $B$ and $X$ respectively?$C_2H_5MgBr$ $\xrightarrow{ClCN} C_2H_5CN$ $\xrightarrow{H_3O^+} B$$CH_3COCH_3$ $\xrightarrow[NaOH]{I_2} X + CHI_3$ $\xrightarrow{Ag} Y$$C_6H_5NH_2$ $\xrightarrow[HCl]{NaNO_2} P$ $\xrightarrow{CuCN} Q$ $\xrightarrow{+4H} R$

Similar Questions

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

$CH_3-CO-CH_2-COOC_2H_5 \xrightarrow{NaOH, H_2O} A$. The product '$A$' in the reaction is

In the given reaction $[X]$ will be :

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 :$A$ $\xrightarrow{LiAlH_{4} / H_{3}O^{+}} B$ $\xrightarrow{\text{Oxidation}} C_{4} \text{ carboxylic acid}$

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

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In the following reactions,what are $B$ and $X$ respectively?
$C_2H_5MgBr$ $\xrightarrow{ClCN} C_2H_5CN$ $\xrightarrow{H_3O^+} B$
$CH_3COCH_3$ $\xrightarrow[NaOH]{I_2} X + CHI_3$ $\xrightarrow{Ag} Y$
$C_6H_5NH_2$ $\xrightarrow[HCl]{NaNO_2} P$ $\xrightarrow{CuCN} Q$ $\xrightarrow{+4H} R$

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 :
$A$ $\xrightarrow{LiAlH_{4} / H_{3}O^{+}} B$ $\xrightarrow{\text{Oxidation}} C_{4} \text{ carboxylic acid}$