Write hydrocarbon radicals that can be formed as intermediates during monochlorination of 2-methylpropane ? Which of them is more stable? Give reasons.

Explanation

To solve the problem of identifying hydrocarbon radicals formed during the monochlorination of 2-methylpropane and determining which is more stable, we can follow these steps:

### Step 1: Draw the Structure of 2-Methylpropane
2-Methylpropane, also known as neopentane, has the following structure:
```
CH3
|
CH3-C-CH3
...