The value of Kc for the thermal decomposition of H₂S is 2.2 x 10⁻⁴ at 1400 K:
2 H₂S(g) ↔ 2 H₂(g) + S₂(g)
initial 3.5 M 0 0
at equilibrium 3.5 M - 2x 2x x
Kc = [S₂][H₂]² / [H₂S]²
2.2 X 10⁻⁴ = x(2x)² / (3.5 - 2x)²
2.2 x 10⁻⁴ = 4 x³ / (3.5)² Assuming x <<<<< 3.5
x = 0.088
Thus [H₂S] = 3.324 M
The lac repressor protein binds to the operator when it is active. The lac repressor is a protein or a DNA-bounding protein as it is called. The lac repressor also involves the lactose metabolism and it is also responsible for the transcription of three lac genes.
The pH of the solution is used to estimate the acidic and the alkaline condition. The pH paper can be used to determine the conditions. The compound with pH 13.3 is basic.
<h3>What is pH?</h3>
The concentration of the hydrogen or the hydroxide ion in the water gives the estimate of the pH. The potential and the amount of hydrogen decide the acidic and the basic compound.
The pH scale ranges from 0-14 where the scale of 0-6 is acidic, 7 is neutral and 8-14 is basic. If the substance shows a pH of 13.3 then it will lie in the basic range.
Therefore, the compound with a pH of 13.3 is basic.
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Answer:
D. The side chains of D-Arg and D-Lys are not positioned to bind correctly at the active site
Explanation:
Stereospecificity is the ability to distinguish between stereoisomers of of a particular compound. L- and D- structures of compounds in living organisms are usually present in only one form due to stereospecificity. For example, naturally occuring amino acids in proteins are usually present as L-isomers.
Since enzyme are proteins, their active sites are composed of L-amino acid and they show stereospecificity in the reactions they catalyze. In their binding sites, only substrates complementary in structure can bind in order for catalysis to proceed. Therefore, only amino acids in the L- configuration are complementary to the active site of enzymes.
In the case of serine proteases, The side chains of -Arg and D-Lys will not be positioned properly for binding at the binding site of serine proteases, therefore, no catalysis will occur. On the other hand, L-Arg and L-Lys can bind to the catalytic site of serine proteases since they are complementary fits to the active site of the enzymes.
There are <u>118</u> elements.