(B) The hydrolysis of acetonitrile $(CH_3CN)$ in an acidic medium proceeds in two steps: $1$. Partial hydrolysis to form acetamide $(CH_3CONH_2)$. $2$

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(B) The hydrolysis of acetonitrile $(CH_3CN)$ in an acidic medium proceeds in two steps: $1$. Partial hydrolysis to form acetamide $(CH_3CONH_2)$. $2$. Complete hydrolysis to form acetic acid $(CH_3COOH)$. In the presence of an acidic medium,the reaction is: $CH_3-CN + 2H_2O \xrightarrow{H^+} CH_3-COOH + NH_4^+$

Class 12 Chemistry 8-2.Carboxylic acids and Their derivative Preparation of Carboxylic Acids and Their Derivatives

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Hydrolysis of acetonitrile in acidic medium gives

A
$CH_3-CH_2-NH_2$
B
$CH_3-COOH$
C
$CH_3-CONH_2$
D
$CH_3-CHO$

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8-2.Carboxylic acids and Their derivative

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Preparation of Carboxylic Acids and Their Derivatives

$R-CH_2-CH_2OH$ can be converted into $R-CH_2-CH_2-COOH$. The correct sequence of the reagents is:

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Acetic acid is obtained when:

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Which reaction is suitable for the preparation of $\alpha$-chloroacetic acid?

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Identify an appropriate reagent for the conversion of $1^o$ Alcohol to carboxylic acid:-

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Identify the product $X$ in the following reaction.
$CH_3COCl \xrightarrow{H_2O} X$

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Hydrolysis of acetonitrile in acidic medium gives

Similar Questions

$R-CH_2-CH_2OH$ can be converted into $R-CH_2-CH_2-COOH$. The correct sequence of the reagents is:

Acetic acid is obtained when:

Which reaction is suitable for the preparation of $\alpha$-chloroacetic acid?

Identify an appropriate reagent for the conversion of $1^o$ Alcohol to carboxylic acid:-

Identify the product $X$ in the following reaction.$CH_3COCl \xrightarrow{H_2O} X$

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Identify the product $X$ in the following reaction.
$CH_3COCl \xrightarrow{H_2O} X$