Given that Eo = -0.34 V for the reduction of Tl+ to Tl, find the voltage developed by a cell consisting of Tl metal dipping in an aqueous solution that is 0.59 M in Tl+, connected by a porous bridge to a 0.53 M aqueous solution of HCl in contact with a Pt electrode over which H2 gas is bubbling at p = 0.81 bar..
Lower the value of standard reduction potential, then the given electrode acts as anode and higher the value of standard reduction potential, then the given electrode acts as cathode.
a. The anode half reaction (oxidation): Tl(s) -------> Tl(+)(aq) + e- ) *2
The cathode half reaction (reduction): 2H+(aq) + 2e- -----> H2(g)
The overall cell reaction : 2H+(aq) + 2Tl(aq) ---> H2(g) + 2Tl+(aq)
E0cell = Ec - Ea = 0- (-0.34) = 0.34 V
The cell potential of the cell at 25 degree Celsius at diffeerent condition is given by Nernst equation
E = Eo- (0.0591/2)* log([Tl+]^2[H2] /[H+]^2])
= 0.34 - (0.0591/2)*log((0.59)^2*0.80/(0.53)^2)
The potential for the redox reaction below at 25 degrees celsius = 0.34011 v
Given that Eo = -0.34 V for the reduction of Tl+ to Tl, find the voltage...
Given that Eo = -0.34 V for the reduction of Tl+ to Tl, find the voltage developed by a cell consisting of Tl metal dipping in an aqueous solution that is 0.37M in Tl+, connected by a porous bridge to a 0.61 M aqueous solution of HCl in contact with a Pt electrode over which H2 gas is bubbling at p = 0.75 bar.
Given that Eo = -0.34 V for the reduction of Tl+ to Tl, find the voltage developed by a cell consisting of Tl metal dipping in an aqueous solution that is 0.52 M in Tl+, connected by a porous bridge to a 0.56 M aqueous solution of HCl in contact with a Pt electrode over which H2 gas is bubbling at p = 0.85 bar. Please answer in volts.
Given that Eo = -0.34 V for the reduction of Tl+ to Tl, find the voltage developed by a cell consisting of Tl metal dipping in an aqueous solution that is 0.58 M in Tl+, connected by a porous bridge to a 0.42 M aqueous solution of HCl in contact with a Pt electrode over which H2 gas is bubbling at p = 0.78 bar. V The number of significant digits is set to 2; the tolerance is +/-4%
Given two reduction half-reactions: Au3+(aq) + 3 e− ⟶ Au(s) Eo = 1.50 V Tl+(aq) + e− ⟶ Tl(s) Eo = −0.34 V Use the electrode potentials above to calculate Eocell and ∆Gorxn for the reaction below, and determine if it is the reaction for a voltaic cell or an electrolytic cell. Click here for a copy of Final Exam cover sheet. Au(s) + 3 Tl+(aq) ⟶ Au3+(aq) + 3 Tl(s) Eocell for the reaction above is [1.84V, -1.84V, 1.16V,...
(1) In the first part of this lab, you need to determine the half-cell reduction potential of each metal. To do so, an inert electrode is needed. Which probe will you choose to use as the inert electrode and in what solution will you insert the inert probe? Group of answer choices Copper probe in 1 M HCl solution Carbon probe in 0.1 M HCl solution Carbon probe in 1 M HCl solution Copper probe in 0.1 M HCl solution...
Page 3 An electrochemical is prepared from a chromium metal electrode in contact solution of 0.500 M chromium (III) nitrate and a standard hydrogen half-cell elect The two half cells are connected by a porous disk or a KCl salt bridge. Standard Reduction Potentials at 298 K Cr+ (aq) + 3e ----> Cr(s) Cr+ (aq) + e ----> Cr2+ (aq) E° = -0.740 V E° = -0.440 V a) Write the reaction for the cell and calculate the standard free...
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8. Determine the reduction potential for H2O(l) in neutral water: [H"]= [OH = 10? (6 points) (P. = 1 atm) 9. A cobalt electrode is placed in 1.00 L of I M CO(NO3)2(aq) and a chromium electrode is placed in 1.00 L of IM Cr(NO3)3(aq). Electrodes are connected by a wire through a voltmeter and the solutions are connected by a salt bridge. (16 points) a. The reduction reaction will be: b. The oxidation reaction will be: c. The...
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Determine the voltage (V) of the following cell at 25°C: Zn(s) | Zn2+(aq, 0.37 M) || Cl-laq, 0.75 M) C12(g, 0.750 atm)| Pt Standard reduction potentials, 298 K, Aqueous Solution (pH = 0): Cl2(g) + 2e --> 2C1-(aq); E° = +1.36 V Hg2Cl2(s) + 2e --> 2Hg(l) + 2Cl(aq); E° = +0.27 V AgCl(s) + e --> Ag(s) + Cl (aq); E° = +0.22 V Ni2+(aq) + 2e --> Ni(s); E° =...
5. What was the purpose of the NaNO3 solution in this experiment? 6. Could a solution of NaCl be used instead of NaNO3? 7. What was the purpose of FeSO4 solution in this experiment? 8. Could a solution of FeCl, be used instead of FeSO4? 9. Could a solution of NaSO4 be used instead of FeSO4? 10. Calculate the standard cell potential for the spontaneous redox reaction between a Pb(s)/Pb(NO3)2(aq) half-cell and a Ag(s)/AgNO3(aq) half-cell. Which metal would be oxidized?...
need help with the rest of the table
EXPERIMENT 10 DETERMINATION OF THE ELECTROCHEMICAL SERIES PURPOSE To determine the standard cell potential values of several electrochemical coll INTRODUCTION The basis for an electrochemical cell is an oxidation reduction Corredor be divided into two half reactions reaction. This reaction can Oxidation half reaction Gloss of electrons) takes place at the anode, which is the positive electrode that the anions migrate to Chence the name anode) Reduction half reaction (gain of electrons)...