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R-CNoverset(H(3)O^(+))underset("Complete...

`R-CNoverset(H_(3)O^(+))underset("Complete hydrolysis")to Xoverset(NH_(3))underset(Delta)toYoverset((i)Br_(2)+KOH)underset((ii)H_(3)O^(+))toZ`
Identify Z.

A

`R-NH_(2)`

B

`R-CH_2NH_2`

C

`R-overset(O)overset(||)C-NH_2`

D

R-CN

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question step by step, we will follow the transformations outlined in the question and the video transcript. ### Step 1: Complete Hydrolysis of R-CN We start with the compound R-CN (where R is an alkyl group and CN is the nitrile group). The first step is to perform complete hydrolysis using water (H2O) under acidic conditions (H3O+). **Reaction:** \[ R-CN + 2 H_2O \xrightarrow{H_3O^+} R-COOH + NH_4^+ \] **Explanation:** - The nitrile group (CN) is converted to a carboxylic acid (R-COOH) and ammonium ion (NH4+). - The carbon atom in the nitrile group becomes part of the carboxylic acid. ### Step 2: Reaction with Ammonia (NH3) Next, we take the carboxylic acid (R-COOH) and react it with ammonia (NH3) and heat it. **Reaction:** \[ R-COOH + NH_3 \xrightarrow{\Delta} R-CO-NH_2 \] **Explanation:** - The carboxylic acid reacts with ammonia to form an amide (R-CO-NH2). - This reaction involves the formation of an ammonium salt intermediate, which upon heating gives the amide. ### Step 3: Bromination and Hydrolysis Now, we perform the Hofmann degradation on the amide (R-CO-NH2) using bromine (Br2) and potassium hydroxide (KOH). **Reaction:** \[ R-CO-NH_2 + Br_2 + KOH \xrightarrow{} R-COOH + NH_2Br \] **Explanation:** - The amide undergoes bromination, leading to the formation of a carboxylic acid (R-COOH) and bromoamine (NH2Br). - The reaction typically results in the loss of one carbon atom from the amide. ### Step 4: Final Hydrolysis Finally, we perform hydrolysis on the bromoamine product. **Reaction:** \[ NH_2Br + H_2O \rightarrow NH_2 + HBr \] **Explanation:** - The bromoamine can be hydrolyzed to produce ammonia (NH2) and hydrobromic acid (HBr). - However, the main product of interest is the carboxylic acid formed earlier. ### Conclusion: Identify Z After performing all the steps, the final product Z is: \[ Z = R-NH_2 + CO_2 \] ### Final Answer Thus, the final product Z is: \[ Z = R-NH_2 + CO_2 \] ---
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