X-linked dominant: a gene on the X chromosome is dominant. Females are more likely to be affected than males since they have 2 X chromosomes that could carry the abnormal gene, whereas a male has just 1. If you know about the Lyon's hypothesis, it states that an X-inactivation renders only one copy of the X-chromosome in each cell therefore only a 1/2 of the cells would have the abnormal gene. So if a father has it o his one X chromosome he can't pass it to his son because his son gets his X chromosome from his mom but the daughter will defenitely have it, if the mother has it. There's a 50% chance a mother with the disorder can pass it to her offspring.
X-linked recessive: just that mutations in a gene on the X-chromosome causes the phenotype to be expressed in hemizygous males and homozygous females.