Color blindness is an X-linked recessive trait. The gene responsible for color blindness is located on the X chromosome. Since males only have one X chromosome, a single recessive allele (X^c) on the X chromosome will cause color blindness. Females have two X chromosomes, so a female must inherit two copies of the color-blind allele (X^c) to be color blind.
(1) In this case, the mother is color blind and has the genotype X^cX^c. The father is normal and has the genotype X^Y.
(2) Sons inherit their Y chromosome from their father and one X chromosome from their mother. Since the mother can only provide a color-blind X chromosome (X^c), all the sons will be color blind (X^cY).
(3) Daughters inherit one X chromosome from each parent. The father provides a normal X chromosome (X), and the mother provides a color-blind X^c chromosome. Thus, the daughters will either be normal (XX) or carriers (X^cX), but not color blind.
Conclusion:
The offspring of a color-blind mother and a normal father will have color-blind sons and normal/carrier daughters.