Answer:
2.9 M
Explanation:
Step 1: Given data
Moles of barium chloride (solute): 4.4 moles
Volume of solution: 1.5 liters
Step 2: Calculate the molarity of barium chloride in the solution
The molarity is a way to quantitatively express the concentration of a solute in a solution. The molarity is equal to the moles of solute divided by the volume, in liters, of solution.

I found this on google
“The periodic table is important because its is organized to provide a great deal of information about elements and how they relate to one another in one-easy-to-use reference. The table can be used to predict the properties of elements, even those that have not been discovered.”
I hope this helps
Answer:
a. Gly-Lys + Leu-Ala-Cys-Arg + Ala-Phe
b. Glu-Ala-Phe + Gly-Ala-Tyr
Explanation:
In this case, we have to remember which peptidic bonds can break each protease:
-) <u>Trypsin</u>
It breaks selectively the peptidic bond in the carbonyl group of lysine or arginine.
-) <u>Chymotrypsin</u>
It breaks selectively the peptidic bond in the carbonyl group of phenylalanine, tryptophan, or tyrosine.
With this in mind in "peptide a", the peptidic bonds that would be broken are the ones in the <u>"Lis"</u> and <u>"Arg"</u> (See figure 1).
In "peptide b", the peptidic bond that would be broken is the one in the <u>"Phe"</u> (See figure 2). The second amino acid that can be broken is <u>tyrosine</u>, but this amino acid is placed in the <u>C terminal spot</u>, therefore will not be involved in the <u>hydrolysis</u>.
Delta H of solution = -Lattice Energy + Hydration
<span>Delta H of solution=- (-730)+(-793) </span>
<span>Delta H of solution= -63kJ/mol </span>
<span>Now we find moles of LiI: </span>
<span>10gLiI/133.85g=.075moles </span>
<span>multiply moles to the delta H of solution to cross cancel moles. .75moles x -64kJ/mol =4.7</span>
Answer:
Inhibitor
Explanation:
Enzyme inhibitors are compounds that can interact with the enzyme but don't trigger any biological response. This is what sulfanilamide does. When the enzyme is bound to sulfanilamide, it stops being able to bind PABA, its normal substrate, and so it cannot perform its biological action. In consequence, the entire biosynthetic pathway for folic acid is stopped.