Answer:
Ok:
Explanation:
So, you can use the Henderson-Hasselbalch equation for this:
pH = pKa + log(
) where A- is the conjugate base of the acid. In other words, A- is the deprotonated form and HA is the protonated.
We can solve that
1 = log(
) and so 10 =
or 10HA = A-. For every 1 protonated form of adenosine (HA), there are 10 A-. So, the percent in the protonated form will be 1(1+10) or 1/11 which is close to 9 percent.
Fossil fuels are buried geologic deposits of organic materials. They are made of decaying plants and animals that have been turned into to natural oil. A few examples of fossil fuels are coal and oil.
When sodium amide i.e.
reacts with water i.e.
results in the formation of sodium hydroxide i.e.
and ammonia
.
The chemical reaction is given by:

Now, when ammonia i.e.
reacts with water results in the formation of ammonium hydroxide i.e. 
The chemical reaction is given by:

Thus, the products of the above reactions are ammonia and ammonium hydroxide (without sodium ion).
The structures of the products are shown in figure (1): ammonium hydroxide and figure (2) ammonia.
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>.