Answer:
yes; and because of how roughly they are played.
Explanation:
Answer:

Explanation:
For a first order reaction the rate law is:
![v=\frac{-d[A]}{[A]}=k[A]](https://tex.z-dn.net/?f=v%3D%5Cfrac%7B-d%5BA%5D%7D%7B%5BA%5D%7D%3Dk%5BA%5D)
Integranting both sides of the equation we get:
![\int\limits^a_b {\frac{d[A]}{[A]}} \, dx =-k\int\limits^t_0 {} \, dt](https://tex.z-dn.net/?f=%5Cint%5Climits%5Ea_b%20%7B%5Cfrac%7Bd%5BA%5D%7D%7B%5BA%5D%7D%7D%20%5C%2C%20dx%20%3D-k%5Cint%5Climits%5Et_0%20%7B%7D%20%5C%2C%20dt)
where "a" stands for [A] (molar concentration of a given reagent) and "b" is {A]0 (initial molar concentration of a given reagent), "t" is the time in seconds.
From that integral we get the integrated rate law:
![ln\frac{[A]}{[A]_{0} } =-kt](https://tex.z-dn.net/?f=ln%5Cfrac%7B%5BA%5D%7D%7B%5BA%5D_%7B0%7D%20%7D%20%3D-kt)
![[A]=[A]_{0}e^{-kt}](https://tex.z-dn.net/?f=%5BA%5D%3D%5BA%5D_%7B0%7De%5E%7B-kt%7D)
![ln[A]=ln[A]_{0} -kt](https://tex.z-dn.net/?f=ln%5BA%5D%3Dln%5BA%5D_%7B0%7D%20-kt)
![k=\frac{ln[A]_{0}-ln[A]}{t}](https://tex.z-dn.net/?f=k%3D%5Cfrac%7Bln%5BA%5D_%7B0%7D-ln%5BA%5D%7D%7Bt%7D)
therefore k is

Molarity is given as,
Molarity = Moles / Volume of Solution ----- (1)
Also, Moles is given as,
Moles = Mass / M.mass
Substituting value of moles in eq. 1,
Molarity = Mass / M.mass × Volume
Solving for Mass,
Mass = Molarity × M.mass × Volume ---- (2)
Data Given;
Molarity = 2.8 mol.L⁻¹
M.mass = 101.5 g.mol⁻¹
Volume = 1 L (I have assumed it because it is not given)
Putting values in eq. 2,
Mass = 2.8 mol.L⁻¹ × 101.5 g.mol⁻¹ × 1 L
Mass = 284.2 g of CuF₂
3 *0.75 = 2.25 mol that’s is ur answer for this question