Answer:
[Ag⁺] = 1.10x10⁻²³ M
Step-by-step explanation:
The equilibrium that takes place is:
Ag⁺ + 2CN⁻ ↔ [Ag(CN)₂]⁻
Kf = 1.0x10²¹ =
![([Ag(CN)_(2)])/([Ag^(+)][CN^(-)]^2)](https://img.qammunity.org/2020/formulas/chemistry/college/k3dalq8m7nur1qxw6e7wlvvogjwpcjxw2r.png)
We calculate the moles of each reagent:
Ag⁺ ⇒ 90.0 L * 0.21 M = 18.9 moles Ag⁺
CN⁻ ⇒ 90.0 L * 5.0 M = 450 moles CN⁻
Because Ag⁺ is the limiting reactant, we use that value to calculate the moles of [Ag(CN)₂]⁻ formed.
We assume 18.9 moles of [Ag(CN)₂]⁻ are formed, because Kf is quite large.
The moles of CN⁻ that reacted are:
18.9 molAg⁺ * 2molCN⁻/1molAg⁺ = 37.8 moles CN⁻
So the remaining CN⁻ moles in solution are 450-37.8 = 412.2 mol CN⁻
The final volume is 99.0 L, so now we recalculate the molar concentrations of CN⁻ and the complex:
412.2 mol CN⁻ / 99L = 4.16 M
18.9 mol [Ag(CN)₂]⁻ / 99L = 0.19 M
Finally we put the data for the complex and [CN⁻] in the expression of Kf and solve for [Ag⁺]:
= 1.0x10²¹
= 1.0x10²¹
[Ag⁺] = 1.10x10⁻²³ M