Answer:
rate = k[A][B] where k = k₂K
Explanation:
Your mechanism is a slow step with a prior equilibrium:
![\begin{array}{rrcl}\text{Step 1}:& \text{A + B} & \xrightarrow [k_{-1}]{k_{1}} & \text{C}\\\text{Step 2}: & \text{C + A} & \xrightarrow [ ]{k_{2}} & \text{D}\\\text{Overall}: & \text{2A + B} & \longrightarrow \, & \text{D}\\\end{array}](https://tex.z-dn.net/?f=%5Cbegin%7Barray%7D%7Brrcl%7D%5Ctext%7BStep%201%7D%3A%26%20%5Ctext%7BA%20%2B%20B%7D%20%26%20%5Cxrightarrow%20%5Bk_%7B-1%7D%5D%7Bk_%7B1%7D%7D%20%26%20%5Ctext%7BC%7D%5C%5C%5Ctext%7BStep%202%7D%3A%20%26%20%5Ctext%7BC%20%2B%20A%7D%20%26%20%5Cxrightarrow%20%5B%20%5D%7Bk_%7B2%7D%7D%20%26%20%5Ctext%7BD%7D%5C%5C%5Ctext%7BOverall%7D%3A%20%26%20%5Ctext%7B2A%20%2B%20B%7D%20%26%20%5Clongrightarrow%20%5C%2C%20%26%20%5Ctext%7BD%7D%5C%5C%5Cend%7Barray%7D)
(The arrow in Step 1 should be equilibrium arrows).
1. Write the rate equations:
![-\dfrac{\text{d[A]}}{\text{d}t} = -\dfrac{\text{d[B]}}{\text{d}t} = -k_{1}[\text{A}][\text{B}] + k_{1}[\text{C}]\\\\\dfrac{\text{d[C]}}{\text{d}t} = k_{1}[\text{A}][\text{B}] - k_{2}[\text{C}]\\\\\dfrac{\text{d[D]}}{\text{d}t} = k_{2}[\text{C}]](https://tex.z-dn.net/?f=-%5Cdfrac%7B%5Ctext%7Bd%5BA%5D%7D%7D%7B%5Ctext%7Bd%7Dt%7D%20%3D%20-%5Cdfrac%7B%5Ctext%7Bd%5BB%5D%7D%7D%7B%5Ctext%7Bd%7Dt%7D%20%3D%20-k_%7B1%7D%5B%5Ctext%7BA%7D%5D%5B%5Ctext%7BB%7D%5D%20%2B%20k_%7B1%7D%5B%5Ctext%7BC%7D%5D%5C%5C%5C%5C%5Cdfrac%7B%5Ctext%7Bd%5BC%5D%7D%7D%7B%5Ctext%7Bd%7Dt%7D%20%3D%20k_%7B1%7D%5B%5Ctext%7BA%7D%5D%5B%5Ctext%7BB%7D%5D%20-%20k_%7B2%7D%5B%5Ctext%7BC%7D%5D%5C%5C%5C%5C%5Cdfrac%7B%5Ctext%7Bd%5BD%5D%7D%7D%7B%5Ctext%7Bd%7Dt%7D%20%3D%20k_%7B2%7D%5B%5Ctext%7BC%7D%5D)
2. Derive the rate law
Assume k₋₁ ≫ k₂.
Then, in effect, we have an equilibrium that is only slightly disturbed by C slowly reacting to form D.
In an equilibrium, the forward and reverse rates are equal:
k₁[A][B] = k₋₁[C]
[C] = (k₁/k₋₁)[A][B] = K[A][B] (K is the equilibrium constant)
rate = d[D]/dt = k₂[C] = k₂K[A][B] = k[A][B]
The rate law is
rate = k[A][B] where k = k₂K
Answer:
I would put, A substance has two different parts of it, a pure substance and a compound and mixtures have two as well called, homogenous mixtures and hetrogeneous mixtures.
Explanation:
Just look it up on google kodvjkngkrefsnjkvjfrnefsjkj
Answer:
The activation energy for the decomposition = 33813.28 J/mol
Explanation:
Using the expression,
Wherem
is the activation energy
R is Gas constant having value = 8.314 J / K mol
Thus, given that, = ?
The conversion of T( °C) to T(K) is shown below:
T(K) = T( °C) + 273.15
So,
T = (5 + 273.15) K = 278.15 K
T = (25 + 273.15) K = 298.15 K
So,
<u>The activation energy for the decomposition = 33813.28 J/mol</u>
We can calculate how long the decay by using the half-life equation. It is expressed as:
A = Ao e^-kt
<span>where A is the amount left at t years, Ao is the initial concentration, and k is a constant.
</span><span>From the half-life data, we can calculate for k.
</span>
1/2(Ao) = Ao e^-k(30)
<span>k = 0.023
</span>
0.04Ao = Ao e^0.023(t)
<span>t = 140 sec</span>
