The following data were measured using a nickel electrode as the standard:
Cu2+(aq) + 2e- ⟶ Cu(s) Ni2+(aq) + 2e- ⟶ Ni(s) Fe2+(aq) + 2e- ⟶ Fe(s) Al3+(aq) + 3e- ⟶ Al(s)
The copper and aluminum electrodes are connected in a battery.
A) Which is the anode? Cathode? Why?
B) Which is oxidized? Reduced? Why?
C) What will the battery voltage be?
Eo =0.62V Eo =0.00V Eo =-0.15V Eo =-1.38V
D) Write a balanced net ionic equation for the reaction that takes place.
More negative reduction potential having stronger reducing agent i.e oxidation takes place at anode and more positive reduction potential having stronger oxidising agent i.e. reduction takes place at cathode.
Among copper and aluminium electrodes
The one with the more negative reduction potential is Aluminium acts as anode and get oxidised .
The one with more positive reduction potential is copper that acts as cathode and get reduced.
Battery voltage, Ecell = Ecathode + Eanode (when sign is changed) = 1.38 V + 0.62 V = +1.97 V
Balanced net ionic equation :
Oxidation half reaction : Al(s) ---> Al+3(aq) + 3e- x 2 = 2Al(s) ---> 2Al+3(aq) + 6e-
Reduction half reaction : Cu+2(aq) + 2e- ----> Cu(s) x 3 = 3Cu+2(aq) + 6e- ----> 3Cu(s)
Balanced net ionic reaction : 2Al(s) + 3Cu+2(aq) ------> 2Al+3(aq) + 3Cu(s)
The following data were measured using a nickel electrode as the standard: Cu2+(aq) + 2e- ⟶...
Use the tabulated electrode potentials to calculate K for the oxidation of nickel by H+: Ni(s)+2H+(aq)→Ni2+(aq)+H2(g) Express your answer using two significant figures. Standard reduction half-cell potentials at 25∘C Half-reaction E∘ (V) Half-reaction E∘ (V) Au3+(aq)+3e−→Au(s) 1.50 Fe2+(aq)+2e−→Fe(s) −0.45 Ag+(aq)+e−→Ag(s) 0.80 Cr3+(aq)+e−→Cr2+(aq) −0.50 Fe3+(aq)+3e−→Fe2+(aq) 0.77 Cr3+(aq)+3e−→Cr(s) −0.73 Cu+(aq)+e−→Cu(s) 0.52 Zn2+(aq)+2e−→Zn(s) −0.76 Cu2+(aq)+2e−→Cu(s) 0.34 Mn2+(aq)+2e−→Mn(s) −1.18 2H+(aq)+2e−→H2(g) 0.00 Al3+(aq)+3e−→Al(s) −1.66 Fe3+(aq)+3e−→Fe(s) −0.036 Mg2+(aq)+2e−→Mg(s) −2.37 Pb2+(aq)+2e−→Pb(s) −0.13 Na+(aq)+e−→Na(s) −2.71 Sn2+(aq)+2e−→Sn(s) −0.14 Ca2+(aq)+2e−→Ca(s) −2.76 Ni2+(aq)+2e−→Ni(s) −0.23 Ba2+(aq)+2e−→Ba(s) −2.90 Co2+(aq)+2e−→Co(s) −0.28 K+(aq)+e−→K(s) −2.92 Cd2+(aq)+2e−→Cd(s)...
Half-cell Potentials: Half Reaction: E value +0.80 V Agt + e → Ag Fe3+ + € → Fe2+ +0.77 v +0.34 V -0.13 V Cu2+ +2e → Cu Pb2+ + 2e - → Ib Ni2+ + 2e → Ni Cd2+ +2e → Cd -0.25 V -0.40 V Fe2+ + 2e → Fe -0.44 V Zn2+ + 2e → Zn -0.76 V Al3+ +3e → AI - 1.66 V Consider an electrochemical cell constructed from the following half cells, linked by...
A) Use tabulated electrode potentials to calculate ΔG∘ for the reaction. 2K(s)+2H2O(l)→H2(g)+2OH−(aq)+2K+(aq) B) (Refer to the following standard reduction half-cell potentials at 25∘C: VO2+(aq)+Ni2+(aq)2H+(aq)++2e−e−→ →Ni(s)VO2+(aq) +H2O(l)E∘=−0.23V E∘=0.99V) An electrochemical cell is based on these two half-reactions: Oxidation:Reduction:Ni(s)VO2+(aq,0.024M)+2H+(aq,1.4M)+e−→→Ni2+(aq,1.8M)+2e−VO2+(aq,1.8M)+H2O(l) Calculate the cell potential under these nonstandard concentrations. C) Standard reduction half-cell potentials at 25∘C Half-reaction E∘ (V ) Half-reaction E∘ (V ) Au3+(aq)+3e−→Au(s) 1.50 Fe2+(aq)+2e−→Fe(s) − 0.45 Ag+(aq)+e−→Ag(s) 0.80 Cr3+(aq)+e−→Cr2+(aq) − 0.50 Fe3+(aq)+3e−→Fe2+(aq) 0.77 Cr3+(aq)+3e−→Cr(s) − 0.73 Cu+(aq)+e−→Cu(s) 0.52 Zn2+(aq)+2e−→Zn(s) − 0.76...
Consider the following electrochemical cell: Al (s) I Al3+ (aq) (1.00 M) II Cu2+ (aq) (0.0020 M) I Cu (s) where Cu2+ aq + 2e- -> Cu (s) +0.34 V and Al3+ aq + 3e- -> Al (s) -1.66 V Calculate the standard cell potential for the given cell, calculate the cell potential for the given cell, and sketch the electrochemical cell using two beakers and labeling the electrodes, the cathode, the anode, the direction of electron flow in the...
NO−3(aq)+4H+(aq)+3e−→NO(g)+2H2O(l) E∘=0.96V ClO2(g)+e−→ClO−2(aq) E∘=0.95V Cu2+(aq)+2e−→Cu(s) E∘=0.34V 2H+(aq)+2e−→H2(g) E∘=0.00V Pb2+(aq)+2e−→Pb(s) E∘=−0.13V Fe2+(aq)+2e−→Fe(s) E∘=−0.45V You may want to reference (Pages 898 - 902) Section 19.4 while completing this problem. Part A Use data from the table above to calculate E∘cell for the reaction. Fe(s)+2H+(aq)→Fe2+(aq)+H2(g) Express your answer using two decimal places.
question iii 10. An electrochemical cell consists of a standard Fe/Fe electrode (Fe (aq) (1.OM) IFe (aq) (1.0M) IPt(s) and a copper metal electrode ( concentrations) Cu2 (aq) +2e Cu(s) Fe (aq) le Fe (aq) +0.34 V -034 +0.77V Mark what is the corect balanced equation for the spontaneous reac u (aq) Fe (aq) Cu(s)+Fe2 (aq) C) Cu(s) + Fe (aq) Cu (aq) + Fe (aq) α Cu2+(aq) + 2e → Cu(s) + Fe2+(aq) Cu → Cu2ト+20 94 i) (...
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salt bridge ME Cr(s) electrode Cu(s) electrode 1.0 M Cr3+ (aq) 1.0 M Cu2+ (aq) A electrolytic cell similar to that shown in the figure above is constructed. The electronic device shown at the top of the figure is a power supply. One electrode compartment consists of a chromium strip placed in a 1.0 M CrCl3 solution, and the other has a copper strip placed in a 1.0 M CuSO4 solution. The overall cell reaction is: 2 Cr3+ (aq) +...
Candidate l: Zn(s) | Zn2+(aq,0.500 M) I Cu2+(aq, 1.00 M) Cu(s) Candidate 2: Pb(s) | Pb2+(aq, 0.500 M) || Cu2+(aq, 1.00 M) Cu(s) Candidate 3: Mg(s) | Mg2+(aq, 0.500 M) | Pb2+(aq, 1.00 M)| Pb(s) (a) 6 pts) Choose one of the candidate voltaic cells #1, #2, or #3. Draw a schematic cell diagram for the candidate voltaic cell of choice. Clearly label anode, cathode, electrodes, ions and their concentrations, salt bridge, and the flow of electrons. (b) (5 pts)...
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