Reduction of methyl isocyanide gives

Options

A. Ethylamine
B. Methylamine
C. Dimethylamine
D. Trimethylamine

Explanation

To solve the question regarding the reduction of methyl isocyanide, we can follow these steps:

### Step 1: Identify the Structure of Methyl Isocyanide
Methyl isocyanide has the chemical formula \( CH_3N \equiv C \). It consists of a methyl group (–CH3) attached to an isocyanide functional group (–N≡C).

### Step 2: Understand the Reduction Process
The reduction of methyl isocyanide involves the addition of hydrogen (H) to the isocyanide group. A strong reducing agent such as Lithium Aluminium Hydride (LiAlH4) is typically used for this purpose.

### Step 3: Apply the Reduction Reaction
When methyl isocyanide is reduced, the isocyanide group (–N≡C) is converted into an amine. The reaction can be represented as follows:

\[ CH_3N \equiv C + 4H \xrightarrow{LiAlH_4} CH_3-NH-CH_3 \]

### Step 4: Identify the Product
The product formed from the reduction of methyl isocyanide is dimethylamine, which has the structure \( (CH_3)_2NH \). This is a secondary amine.

### Step 5: Conclusion
Thus, the reduction of methyl isocyanide gives dimethylamine.

### Final Answer:
The reduction of methyl isocyanide gives **dimethylamine**.

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