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CH(3)CH(2)COONH(4)overset(P(2)O(5))under...

`CH_(3)CH_(2)COONH_(4)overset(P_(2)O_(5))underset(Delta)toXoverset(H^(+)//H_(2)O)toY`.
Y and X respectively are

A

`CH_(3)CH_(2)COOH,CH_(3)CH_(2)CN`

B

`CH_(3)CH_(2)CN,CH_(3)CH_(2)COOH`

C

`CH_(3)CH_(2)CH_(2)COOH,CH_(3)CH_(2)CH_(3)`

D

`CH_(3)CH_(3),CH_(3)CH_(2)COOCH_(3)`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we will analyze the given reaction step by step. ### Step 1: Identify the starting compound The starting compound is CH₃CH₂COONH₄, which is ammonium propionate. ### Step 2: Heating with P₂O₅ When ammonium propionate is heated in the presence of phosphorus pentoxide (P₂O₅), a dehydrating agent, it undergoes dehydration. The reaction removes a water molecule (H₂O) and converts the ammonium salt into an amide. The reaction can be represented as: \[ \text{CH}_3\text{CH}_2\text{COONH}_4 \xrightarrow{\Delta, P_2O_5} \text{CH}_3\text{CH}_2\text{CONH}_2 + \text{H}_2\text{O} \] Here, CH₃CH₂CONH₂ is propanamide (an amide). ### Step 3: Identify compound X After the dehydration step, we have formed propanamide (CH₃CH₂CONH₂). Therefore, X is: \[ X = \text{CH}_3\text{CH}_2\text{CONH}_2 \] ### Step 4: Hydrolysis of X Next, we perform hydrolysis of the amide (X) using H⁺ and H₂O. Hydrolysis of an amide typically results in the formation of a carboxylic acid and ammonia. The reaction can be represented as: \[ \text{CH}_3\text{CH}_2\text{CONH}_2 + H_2O \xrightarrow{H^+} \text{CH}_3\text{CH}_2\text{COOH} + \text{NH}_3 \] Here, CH₃CH₂COOH is propanoic acid. ### Step 5: Identify compound Y After hydrolysis, we have formed propanoic acid (CH₃CH₂COOH) and ammonia (NH₃). Therefore, Y is: \[ Y = \text{CH}_3\text{CH}_2\text{COOH} \] ### Final Answer Thus, the final answers are: - X = CH₃CH₂CONH₂ (propanamide) - Y = CH₃CH₂COOH (propanoic acid)
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