No... From blossom. Is your answer
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>.
Answer:
55.18 L
Explanation:
First we convert 113.4 g of NO₂ into moles, using its molar mass:
- 113.4 g ÷ 46 g/mol = 2.465 mol
Then we<u> use the PV=nRT formula</u>, where:
- P = 1atm & T = 273K (This means STP)
- R = 0.082 atm·L·mol⁻¹·K⁻¹
Input the data:
- 1 atm * V = 2.465 mol * 0.082atm·L·mol⁻¹·K⁻¹ * 273 K
And <u>solve for V</u>:
increasing the temperature shifts the equilibrium in the direction of the reaction in which heat is absorbed.
Explanation:
The concentration of NO at equilibrium will increase when the reaction takes place at a higher temperature because increasing the temperature shifts the equilibrium in the direction of the reaction in which heat is absorbed.
The reaction is an endothermic reaction.
N₂ + O₂ + heat ⇄ 2NO
According to Le Chatelier's principle, "if any of the conditions of a system in equilibrium is changed the system will adjust itself in order to annul the effect of the change".
- In an endothermic reaction, heat is usually absorbed.
- We see that in the backward reaction, heat is absorbed.
- If the temperature of this reaction is increased, the backward reaction is favored more.
- Since the reactants are combining better, more products NO results.
learn more:
Thermodynamics of reactions brainly.com/question/10567109
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In general chemistry, isomers are two or more elements that have the same number of protons but differ in mass number. In organic chemistry, the compounds are cis or trans isomers if they have the same chemical formula, but differ in the placement of functional groups based on molecular geometry. Cis isomer is when two like functional groups are on the same side of the molecules, while trans isomer is when the like functional groups are on opposite sides.
The cis-trans isomers are shown in the picture. As you can see, in the cis isomer, the methane functional group are both in the same side. Same as well with the hydrogen atoms. On the other hand, these functional groups are opposite to each other in the trans isomer.