Complete a chair conformation of trans-1-bromo-3-methylcyclohexane by placing the hydrogen, bromine, and methyl groups in the appropriate positions. Place the bromine on the carbon that is more to the right.

Explanation:

The most highly stable cycloalkane is cyclohexane. It does not suffer from an angle or torsional strain, and it has the appropriate stability as chain alkanes. Because of the peculiar conformation it takes, this stability leads to the cyclohexane conformation popularly known as the "chair" conformation.

However, from the information given;

The chair conformation structure of  trans-1-bromo-3-methylcyclohexane is carefully drawn and the substituents are appropriately attached in the image below.

- "the choice that is not an indicator of a chemical change is "state of matter changes". more common than not, chemical reactions produce energy in the form of light or heat. along with energy, they also produce a new substance called the product that could be in any state of matter (solid, gas, or liquid)."