CHEMISTRY 115 HOMEWORK 5 NAME _______________
Due MAY 9, 01 COMP HWK: Electro: 1-4
__ K2Cr2O7 + __ FeCl2 + __ HCl -> __ CrCl3 + __ H2O + __ FeCl3 + __ KCl
Cr2O72- + Fe2+ --acid-> Cr3+ + Fe3+
6 e- + 6 H+ + 8 HCl + K2Cr2O7 à 2 CrCl3 + 2 KCl + 7 H2O
6[HCl + FeCl2 à FeCl3 + H+ + e-]
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14 HCl + K2Cr2O7 + 6 FeCl2 à 2 CrCl3 + 2 KCl + 7 H2O + 6 FeCl3
6 e- + 14 H+ + Cr2O72- à 2 Cr3+ + 7 H2O
6[Fe2+ à Fe3+ + e-]
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14 H+ + Cr2O72- + 6 Fe2+ à 2 Cr3+ + 7 H2O + 6 Fe3+
Write out as full compounds and balance the K’s and Cl’s
Chemical species oxidized: loses e- = Fe2+ = FeCl2, Oxidizing agent: gains e+ = Cr2O72- = K2Cr2O7
2. Write the half reactions and a balanced reaction for the following galvanic cell.
Fe (s)| Fe+2 (aq)|| Br2(aq), Br-(aq) | Pt(s)
Fe(s) = Fe2+ + 2 e-
Br2 + 2 e- = 2 Br-
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Fe(s) + Br2 = Fe2+ + 2 Br-
3. Write cell notation for the following galvanic cell, If reactants are in solution or are gases assume a platinum electrode.
NiO2(s) + 4H+(aq) + 2Ag(s) à Ni+2(aq) + H2O + 2Ag+
Ag(s) | Ag+ || NiO2(s), Ni2+., H+ | Pt(s)
4a. Circle the better oxidizing agent in the following pairs at standard conditions.
More easily reduced = higher (more positive) on the reduction emf table.
I. Fe3+ or Pb2+ |
II. I2 or Sn2+ |
III. MnO4- or Cr2O72- |
+0.77 vs -0.13 |
+0.54 vs – 0.14 |
+1.49 (1.507) vs +1.33 |
b. Circle the better reducing agent in the following pairs at standard conditions.
More easily oxidized = lower (more negative) on the reduction emf table on right side.
I. H2 or I- |
II. Sn2+ or Fe2+ |
III. Sn2+ or Cu |
0.0 vs –(+0.54) |
-(+0.15) vs –(+0.77) |
-(+0.15) vs –(+0.34) |
5. Label the sketch of a voltaic cell below showing the anode, the cathode, the signs of the electrodes, and the direction of electron flow. Also give the overall chemical reaction and calculate the standard electrode potential for the cell. (The cell is not necessarily drawn as anode, cathode.)
Pt|Br2(l)|Br-(aq)||Cl-(aq)|Cl2(g)|Pt or its reverse, i.e. the one which corresponds to the spontaneous reaction. For a voltaic or galvanic cell, the overall emf must be positive
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e-à |
e- à |
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Br2(l), Br-(1M) |
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Cl2(1atm),Cl-(1M) |
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Oxidation = |
anode |
Reduction = |
cathode |
Cl2 + 2 e- = 2 Cl- |
e0 = +1.36 V |
2 Br- = Br2 + 2 e- |
eo = -(+1.07 v) |
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e0 = 0.29 V |
Eo = |_0.29 V_____
Reaction:__Cl2 + 2 Br- = 2 Cl- + Br2_________________________________
MnO2 + 4H+ + 2e- ó Mn+2 + 2H2O |
Eo = 1.23 V |
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PbCl2 + 2e- ó Pb + 2Cl- |
Eo = -0.27 V |
Pb reaction must be reversed for the oxidation and give a + emf
MnO2 + 4H+ + 2e- ó Mn+2 + 2H2O |
Eo = 1.23 V |
Pb + 2 Cl- = PbCl2 + 2 e- |
Eo = +0.27 V |
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MnO2 + 4 H+ + Pb + 2 Cl- = Mn2+ + 2 H2O + PbCl2 |
Eo = 1.50 V |
Eo = |_1.50 V______
HClO(aq) + H+(aq) + 2 e- = Cl-(aq) + H2O(l) |
eo = ? |
Reverse 2[Cr3+ + e- = Cr2+] |
eo = -(-0.40) |
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HClO(aq) + H+(aq) + 2 Cr2+(aq) = 2 Cr3+(aq) + Cl-(aq) + H2O(l) |
eo = 1.80 V |
Eo = 1.80 V – 0.40 V = 1.40 V
Eo = |__1.40 V____
The Cr3+ + e- = Cr2+ half-reaction that is not given in your text table can be calculated using "skip potentials", a type of short-hand for the DG calculations ( = -nFe), ignoring the constant F
3(Cr3+ + 3 e-= Cr) = 2(Cr2+ + 2 e- = Cr) + 1(Cr3+ + e- = Cr2+)
3(-0.74 V) = 2(-0.91 V) + eo ; eo = -2.22 V – (-1.82 V) = -0.40V