Answer:
The options <u>(A) -</u>The rate law for a given reaction can be determined from a knowledge of the rate-determining step in that reaction's mechanism. and <u>(C) </u>-The rate laws of bimolecular elementary reactions are second order overall ,<u>is true.</u>
Explanation:
(A) -The rate law can only be calculated from the reaction's slowest or rate-determining phase, according to the first sentence.
(B) -The second statement is not entirely right, since we cannot evaluate an accurate rate law by simply looking at the net equation. It must be decided by experimentation.
(C) -Since there are two reactants, the third statement is correct: most bimolecular reactions are second order overall.
(D)-The fourth argument is incorrect. We must track the rates of and elementary phase that is following the reaction in order to determine the rate.
<u>Therefore , the first and third statement is true.</u>
When it’s warmer so when temperature encreases
Answer: The approximate molecular mass of the polypeptide is 856 g/mol
Explanation:
To calculate the concentration of solute, we use the equation for osmotic pressure, which is:
Or,
where,
= osmotic pressure of the solution = 4.19 torr
i = Van't hoff factor = 1 (for non-electrolytes)
Mass of solute (polypeptide) = 0.327 g
Volume of solution = 1.70 L
R = Gas constant =
T = temperature of the solution =
Putting values in above equation, we get:
Hence, the molar mass of the polypeptide is 856 g/mol
<span>NH3 is the answer, if u look up its ph its a weak base</span>
In order to deprotonate an acid, we must remove protons in order to achieve a more stable conjugate base. For this example, we can use the relationship between carboxylic acid and hydroxide.
Deprotonation is the removal of a proton from a specific type of acid in reaction to its coming into contact with a strong base. The compound formed from this reaction is known as the conjugate base of that acid. The opposite process is also possible and is when a proton is added to a special kind of base. This is a process referred to as protonation, which forms the conjugate acid of that base.
For the example we have chosen to give, the conjugate base is the carboxylate salt. This would be the compound formed by the deprotonated carboxylic acid. The base in question was strong enough to deprotonate the acid due to the greater stability offered as a conjugated base.
To learn more visit:
brainly.com/question/5613072?referrer=searchResults