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The standard oxidation potentials for Mn...

The standard oxidation potentials for `Mn^(3+)` ion acid solution are `Mn^(2+)overset(-1.5V)toMn^(3+)overset(-1.0V)toMnO_(2)`. Is the reaction `2Mn^(3+)+2H_(2)OtoMn^(2+)+MnO_(2)+4H^(+)` spontaneous under conditions of unit activity? What is the change in free energy?

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To determine if the reaction \( 2Mn^{3+} + 2H_2O \rightarrow Mn^{2+} + MnO_2 + 4H^+ \) is spontaneous under conditions of unit activity and to calculate the change in free energy (\( \Delta G \)), we can follow these steps: ### Step 1: Identify the half-reactions and their standard potentials The half-reactions and their standard potentials provided are: 1. \( Mn^{2+} + 2e^- \rightarrow Mn^{3+} \) with \( E^\circ = -1.5 \, V \) 2. \( Mn^{3+} + 2e^- \rightarrow MnO_2 + 4H^+ \) with \( E^\circ = -1.0 \, V \) ### Step 2: Write the overall reaction The overall reaction can be derived from the half-reactions: - The reverse of the first half-reaction (oxidation) gives: \[ Mn^{3+} \rightarrow Mn^{2+} + 2e^- \] - The second half-reaction (reduction) is: \[ Mn^{3+} + 2e^- \rightarrow MnO_2 + 4H^+ \] ### Step 3: Combine the half-reactions To combine the half-reactions, we need to ensure that the electrons cancel out. The overall reaction becomes: \[ 2Mn^{3+} + 2H_2O \rightarrow Mn^{2+} + MnO_2 + 4H^+ \] ### Step 4: Calculate the standard cell potential \( E^\circ \) The standard cell potential \( E^\circ \) for the overall reaction can be calculated as follows: \[ E^\circ = E^\circ_{\text{reduction}} - E^\circ_{\text{oxidation}} \] Substituting the values: \[ E^\circ = (-1.0 \, V) - (-1.5 \, V) = -1.0 + 1.5 = 0.5 \, V \] ### Step 5: Calculate the change in free energy \( \Delta G \) The change in free energy can be calculated using the formula: \[ \Delta G = -nFE^\circ \] Where: - \( n \) = number of moles of electrons transferred (which is 2 for this reaction) - \( F \) = Faraday's constant \( \approx 96500 \, C/mol \) - \( E^\circ \) = standard cell potential calculated in the previous step Substituting the values: \[ \Delta G = -2 \times 96500 \, C/mol \times 0.5 \, V = -48250 \, J/mol \] ### Conclusion The reaction is spontaneous because \( \Delta G < 0 \). The change in free energy is \( -48250 \, J/mol \). ---
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The standard oxidation potential for Mn^(3+) ion acid solution are Mn^(2+)overset(-1.5V)rarrMn^(3+) overset(-1.0V)rarr MnO_(2) . Is the reaction 2Mn^(3+)+2H_(2)O rarr Mn^(2+)+MnO_(2)+4H^(+) spontaneous under conditions of unit activity ? What is the change in free energy ?

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What is the hybridisation of Mn in K_(2)MnO_(4) ?

In the reaction KMnO_(4) + H_(2)SO_(4) + H_(2)C_(2)O_(4) to products, Mn^(2+) ions act as:

The standard redox potentials for the reactions, MN^(2+) + 2e^(-)to Mn and Mn^(3+) + e^(-) are -1.18V and 1.51V respectively. What is the redox potential for the reaction Mn^(3+)+ 3e^(-) to Mn ?

In the reaction MnO_(4)^(-)+SO_(3)^(-2)+H^(+)rarrSO_(4)^(-2)+Mn^(2+)+H_(2)O

In the reaction MnO_(4)^(-)+SO_(3)^(-2)+H^(+)rarrSO_(4)^(-2)+Mn^(2+)+H_(2)O

The Mn^(3+) ion is unstable in solution and undergoes disproportionation reaction to give Mn^(+2), MnO_(2) , and H^(o+) ion. Write a balanced ionic equation for the reaction.

Volumetric titrations involving KMnO_(4) , are carried out only in presence of dilute H_(2)SO_(4) but not in the presence of HCI or HNO_(3) This is because oxygen produced from KMnO_(4) + dil: H_(2)SO_(4) , is used only for oxidizing the reducing agent. Moreover, H2SO4 does not give any oxygen of its own to oxidize the reducing agent. In case HCI is used, the oxygen produced from KMnO_(4) + HCI is partly used up to oxidize HCI and in case HNO_(3) is used, it itself acts as oxidizing agent and partly oxidizes the reducing agent. KMnO_(4) , in various mediums gives following products Mn^(7+)overset(H^(+))toMn^(2+) Mn^(7+)overset(H_(2)O)toMn^(4+) Mn^(7+)underset(OH^(-))toMn^(6+) QThe number of moles of KMnO_(4) that will be needed to react with one mole of sulphite in an acidic solution is

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