Answer:
(C) Competitive inhibition
Explanation:
When a substrate competes with and inhibitor, what they are actually doing is competing by the active site of the enzyme. In terms of probabilities, when there is much more of one molecule of X than its competitor Y, it is more likely for any of the molecules of X to reach the active site of the enzyme than for any of the molecules of Y.
Then is one would like to reduce the effects of an inhibitor reversible bonded to an enzyme, one possibility is to increase the concentration of a substrate (which in turn means that there will be a higher relative number of its molecules in the media), increasing the probability to meet the active site of the enzyme and as a result displacing the inhibitor (assuming it not increased as well).
Answer:
a. 8.1 milligrams
b. 40.07 hours
c. 8.859 milligrams
Explanation:
If a person takes a prescribed dose of 10 milligrams of Valium, the amount of Valium in that person's bloodstream at any time can be modeled by

Where A(t) = amount of Valium remaining in the blood after t hours
t = time or duration after the drug is taken
a. we have to calculate the amount of drug remaining in the bloodstream after 12 hours


= 10×0.81253
= 8.1 milligrams
b. In this part we have to calculate the time when A(t) = 5 milligrams


0.5 = 
Now we take natural log on both the sides of the equation.
ln(0.5) = ln(
-0.69314 = -0.0173t
t = 
t = 40.0658
≈ 40.07 hours
c. In this part we have to calculate the rate, by which amount of drug will decay in the bloodstream after 7 hours.


= 10×0.8859
= 8.859 milligrams
It would be Metaphase as the spindle fibers keep them at the equator of the cell then pull them apart in the next phase: Anaphase.
Answer:
because it has something at checks it and allows it to pass
Explanation: