The correct response is:
The mutation is found on the X chromosome, and since males only have one X chromosome, they only need one copy of the mutated gene to have the disorder.
This is why males are more likely to be affected by hemophilia, as they have one X chromosome (XY), and if that X chromosome carries the mutated gene, they will manifest the disorder. In contrast, females have two X chromosomes (XX), so they would need two copies of the mutated gene to express the disorder, making it less likely for them to be affected.