1.

How much `AgBr` could dissolve in `1.0L` of `0.4M NH_(3)`? Assume that `Ag(NH_(3))_(2)^(o+)` is the only complex formed. Given: the dissociation constant for `Ag(NH_(3))_(2)^(o+) hArr Ag^(o+) xx 2NH_(3)`, `K_(d) = 6.0 xx 10^(-8)` and `K_(sp)(AgBr) =5.0 xx 10^(-13)`.

Answer» Let solubility of `AgBr` be `xM`. Thus, `[Br^(Θ)] = xM`, but `[Ag^(o+)] != xM` since it will react with `NH_(3)` to form a complex and thus, its concentration will be decied by the disscoiation of complex. So, let `[Ag^(o+)] = yM`.
`AgBr hArr Ag^(o+)(aq) +Br^(Θ) (aq)`
`rArr K_(sp) = [Ag^(o+)] [Br^(-)] = yx = 5.0 xx 10^(-13)`
Since the formation constant `(K_(f))` of the complex is very high, assume that whole of `Ag^(o+)` formed is consumed.
`{:(Ag^(o+)+,2NH_(3)rarr,Ag(NH_(2))_(2).^(oplus),,),(x,0.4,,,),(,0.4-2x,x,,):}`
`{:(Ag(NH_(3))_(2)^(o+)hArr,Ag^(o+)(aq),+2NH_(3),(K_(d)=5.0xx10^(-13)),,),(x,,0.4-2x,,),(x-y,,y0.4-2x+2y,,):}`
Thus, `K_(d) = ([Ag^(oplus)][NH_(3)]^(2))/([Ag(NH_(3))_(2)^(oplus)])=(y(0.4-2x+2y)^(2))/(x-y) =6xx10^(-8)`
Assuming `x-y ~~` since `K_(d)` is low and `x lt lt 0.4`, we get :
`K_(d) = (y(0.4)^(2))/(x)`
Solving for `x` :
`x = 1.15 xx 10^(-3)M`
(Verify the approximation yourself).


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