Question

Question #933f1

Answer 1

Here's how I would do it.

Explanation:

1. Draw a cyclohexene ring.

2. Attach a methyl group to one of the double-bonded carbons.

That carbon automatically becomes `"C1"` of the ring.

The other double-bonded carbon becomes `"C2"`, and the numbering continues around the ring.

3. Add `"Cl"` atoms to `"C2"` and `"C3"`.

And you have the structure of 2,3-dichloro-1-methylcyclohexene.