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Given that at 25^@C [Ag(NH(3))(2)]^(+)...

Given that at `25^@C`
`[Ag(NH_(3))_(2)]^(+) +e^(0) to Ag_((s))+2NH_(3) E^(0)=0.02V and Ag^(+)+1e^(-) to Ag_((s))" " E^(0)=0.8V`
Hence the order of magnitude of equilibrium constant of the reaction
`[Ag(NH_(3))_(2)]^(+) Leftrightarrow Ag^(+) +2NH_(3)`, will be (antilog 0.22=1.66)

A

`10^(-10)`

B

`10^(-6)`

C

`10^(-14)`

D

`10^(-18)`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to determine the equilibrium constant for the reaction: \[ [Ag(NH_3)_2]^+ \rightleftharpoons Ag^+ + 2NH_3 \] We are given the standard reduction potentials for the following half-reactions: 1. \([Ag(NH_3)_2]^+ + e^- \rightarrow Ag(s) + 2NH_3\) with \(E^\circ = 0.02 \, V\) 2. \(Ag^+ + e^- \rightarrow Ag(s)\) with \(E^\circ = 0.8 \, V\) ### Step 1: Determine the overall cell reaction To find the overall reaction, we need to reverse the first half-reaction since we are looking for the oxidation of \([Ag(NH_3)_2]^+\): \[ Ag(s) + 2NH_3 \rightarrow [Ag(NH_3)_2]^+ + e^- \quad (E^\circ = -0.02 \, V) \] Now, we can combine this with the second half-reaction: \[ Ag^+ + e^- \rightarrow Ag(s) \quad (E^\circ = 0.8 \, V) \] ### Step 2: Write the overall reaction Adding the two half-reactions gives us: \[ [Ag(NH_3)_2]^+ \rightleftharpoons Ag^+ + 2NH_3 \] ### Step 3: Calculate the standard cell potential \(E^\circ_{cell}\) The standard cell potential is calculated by subtracting the oxidation potential from the reduction potential: \[ E^\circ_{cell} = E^\circ_{reduction} - E^\circ_{oxidation} \] Substituting the values: \[ E^\circ_{cell} = 0.8 \, V - (-0.02 \, V) = 0.8 \, V + 0.02 \, V = 0.82 \, V \] ### Step 4: Relate \(E^\circ_{cell}\) to the equilibrium constant \(K\) Using the Nernst equation, we know that: \[ E^\circ_{cell} = \frac{0.0591}{n} \log K \] Where \(n\) is the number of electrons transferred in the reaction. Here, \(n = 1\) (one electron is involved). Rearranging gives us: \[ \log K = \frac{E^\circ_{cell} \cdot n}{0.0591} \] Substituting the values: \[ \log K = \frac{0.82 \cdot 1}{0.0591} \approx 13.9 \] ### Step 5: Calculate \(K\) To find \(K\), we take the antilog: \[ K = 10^{13.9} \approx 7.94 \times 10^{13} \] ### Step 6: Determine the order of magnitude of \(K\) The order of magnitude of \(K\) is \(10^{13}\). ### Final Answer The order of magnitude of the equilibrium constant of the reaction is \(10^{13}\). ---
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Given the data 25^(@) C , Ag+ I^(-) to AgI+e^(-) , E^(@) = 0.152V Ag to Ag^(+) + E(-) , E^(@) = - 0.800V What is the value of K_(sp) for AgI?

Gvien the following value for the standard molar Gibbs free energy changes? G^(@) , at 25^(@)C Ag^(+) (aq) + 2NH_(3) (l) hArr Ag (NH_(3))_(2)^(+) (aq) ? G^(2) = -41.0KJ (mol Ag^(+))^(-1) Ag^(+) (aq) + Cl^(-)(aq) hArr AgCl (s) ? G^(@) = - 55.6 kJ (mol Ag^(+))^(-1) Calculate the value for the thermodynamic equilibrium constant. K, at 25^(@)C for the reactions: AgCl (s) + 2NH_(3) (l) hArr Ag (NH_(3))_(2)^(+) (aq) + Cl (aq)

Ag^(+) + NH_(3) ltimplies [Ag(NH_(3))]^(+), k_(1)=6.8 xx 10^(-5) [Ag(NH_(3))]^(+) + NH_(3) ltimplies [Ag(NH_(3))_(2)]^(+) , k_(2) = 1.6xx10^(-3) The formation constant of [Ag(NH_(3))_(2)]^(+) is :

If Ag^(+)+NH_(3)hArr[Ag(NH_(3))]^(+) , K_(1)=3.5xx10^(-3) and [Ag(NH_(3))]^(+)+NH_(3)hArr[Ag(NH_(3))_(2)]^(+) , K_(2)=1.74xx10^(-3) . The formation constant of [Ag(NH_(3))_(2)]^(+) is :

Ag^(+)+NHP(3)hArr[Ag(NH_(3))]^(+), K_(1)=3.5=10^(-3) [Ag(NH)_(3)]^(+)+NH_(3)hArr[Ag(NH_(3))_(2)]^(+),K_(2)=1.7xx10^(-3) then the formation constant of [Ag(NH_(3))_(2)]^(+) is

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