Answer: 
The correct answer would be 50% .
Red-green colorblindness is an X-linked recessive disorder that is, the mutated gene responsible for this trait is present on the X chromosome. 
Let the "R" and "r" be the alleles of the gene responsible for this trait. 
R is the dominant trait which leads to the normal vision in a person. Thus, heterozygotes will have a normal vision however, they will act as the carrier of the disease. 
r is the recessive allele which causes red-green colorblindness in a person when present in homozygous condition. 
Now, the genotype of the mother with red-green colorblindness would be 
 and the genotype of unaffected father would be
 and the genotype of unaffected father would be 
 .
. 
The cross will result in the production of two daughters each heterozygous and two sons each with the colorblindness. 
The probability of having a son = 1/2. 
The probability of son being colorblind = 1 
Thus, the probability of having a son with colorblindness = 1/2 x 1 = 1/2 or 50%