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On heating benzyl amine with chloroform ...

On heating benzyl amine with chloroform and ethanolic KOH, product obtained is

A

benzyl alcohol

B

benzaldehyde

C

benzonitrile

D

benzyl isocyanide.

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The correct Answer is:
To solve the question, "On heating benzyl amine with chloroform and ethanolic KOH, what product is obtained?", we can follow these steps: ### Step 1: Identify the Reactants The reactants in this reaction are: - Benzyl amine (C6H5CH2NH2) - Chloroform (CHCl3) - Ethanolic potassium hydroxide (KOH in ethanol) ### Step 2: Recognize the Type of Reaction The reaction between a primary amine (like benzyl amine) and chloroform in the presence of a strong base (like ethanolic KOH) is known as the **Carbylamine reaction**. This reaction is specific to primary amines. ### Step 3: Understand the Mechanism In the Carbylamine reaction, the primary amine reacts with chloroform and a strong base to form an isocyanide. The mechanism involves: 1. The base deprotonates the amine, forming an amine anion. 2. The amine anion then reacts with chloroform to form an intermediate. 3. This intermediate rearranges to produce the isocyanide. ### Step 4: Write the Product The product formed from the reaction of benzyl amine with chloroform and ethanolic KOH is **benzyl isocyanide** (C6H5CH2N=C=O). The structure of benzyl isocyanide consists of a benzene ring attached to a CH2 group, which is further connected to an isocyanide functional group (–N=C=O). ### Step 5: Conclusion Thus, the final product obtained from the reaction of benzyl amine with chloroform and ethanolic KOH is **benzyl isocyanide**. ### Final Answer: Benzyl isocyanide (C6H5CH2N=C=O) ---

To solve the question, "On heating benzyl amine with chloroform and ethanolic KOH, what product is obtained?", we can follow these steps: ### Step 1: Identify the Reactants The reactants in this reaction are: - Benzyl amine (C6H5CH2NH2) - Chloroform (CHCl3) - Ethanolic potassium hydroxide (KOH in ethanol) ...
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  14. Nitration of aniline is achieved by

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  16. Electrolytic reduction of nitrobenzene in weakly acidic medium gives .

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