<span>Correct answer: They end up in bodies of water killing animals and plant life. </span>
We know that Hardy-Weinberg conditions include the following equations:

where 
And where p = dominant, and q = recessive; this means that
is equal to the homozygous dominant,
is the heterozygous, and
is the homozygous recessive .
So we have 100 total cats, with 4 having the recessive white coat color. That means we have a ratio of
or 0.04. Let that equal our
value.
So when we solve for q, we get:


Now that we have our q value, we can use the other equation to find p:



So then we can solve for our heterozygous population:

This is the ratio of the population. So we then multiply this number by 100 to get the number of cats that are heterozygous:

So now we know that there are 32 heterozygous cats in the population.
Answer:
A- A pH change can cause the enzyme to change its shape
Explanation:
A rise or fall in the pH of the medium from the optimum of pH 7 usually affect the enzymes' active sites of and therefore the shape and the rate of enzyme activity.
Assuming the pH is too low, the enzyme medium becomes acidic;Acidosis. The high Hydrogen ions concentration interacts with the R-groups of the amino acids moiety of the enzymes, this interaction affects the ionization of the R-groups, disrupting the ionic bonding holding these R-groups in shape.
This results in loss of the 3-Dimensional shape arrangements of the protein molecule and therefore of the active sites. Since active sites of enzymes determines the specificity of the <u>enzymes substrate- complex </u> to give <u>enzyme-product complex,</u> the catalytic activity of the enzymes decreases, <u>the rate of reaction decreases,and products formation stops, and the reaction also stops.</u>
The same is applicable to extremely high pH=Alkalosis.
However, the effective buffer system of the body prevents this scenarios from happening in real sense in the body. Through mopping by the haemoglobin, excretion by the kidney, etc
Answer:
cystic fibrosis, phenylketonuria, hemochromatosis, Bloom's syndrome, and ataxia-telangietasia. The X-linked recessive diseases are due to mutations in genes located on the X chromosome and include Duchenne's muscular dystrophy, Fabry's disease, steroid sulfatase deficiency, and ocular albinism.
Explanation:
First is the second and the other one is the 4th