I have a lot of questions actually.
it's electrochemistry (which is obviously a bunch of fun)
2 electrodes Cr(s)/Cr3+ and Sn(s)/Sn2+ are combined to afford a spontaneous electrochemical reaction. the standard reduction potention in V for Cr3+ and Sn2+ are -.74 and -.14 V respectably. E in V=.....
a. .88 v b. -.88 v c. .60 v d. -.60 v e 2.5 v
calculate delta G for reaction of elemental bromine with chloride ion
Br-->E=1.09
Cl-->E=1.36
a. 2.1x10^5 J b. -2.62x10^5 J c. .27 J d. 5.21x10^4 J
consider the half reaction below. what will happen to E of the half cell if pH increases
2IO3-(aq)+10e-+12H+(aq)->I2(s)+6H2O(l) E=1.195 V
a. increases b. decreases c. no change
standard reduction potential in V for Zn2+ and Cu2+ are -.76 and .34 respectably, what is the potential of the cell below
Zn | Zn2+ (1.0 M) || Cu2+ (.10 M) | Cu
a. -1.14 v b. -.42 v c. 1.0 v d. 1.10 v
standard reduction potential in V for Ag+ and Fe2+ to Fe2+ are .80 and .77 calculate K (equilibrium constant) for the following reaction (R=8.314 J/k mol, F=96800 J/V)
Ag+(aq)+Fe2+(aq)->Ag(s)+Fe3+(aq)
a. .10 b. 2 c. 3.2 d. 1.0
thanks sosomuch if you can help =/ =D
7 answers
Use
E = Eo-(0.059/n)*log (red/ox). Write in the reduced species and oxidized species, and see how an increase of pH will change E.
Calculate E for Zn ==> Zn^+2 + 2e. At 1 M concn Zn^+2, that will be the reverse of the standard reduction potential.
Calculate E for Cu^+2 ==> Cu. For this you must use
E = Eo-(0.059/n)*log(Cu/Cu^+2)
n is 2, Cu = 1, and (Cu^+2) = 0.1 M.
Then add the two E values to obtain the cell value.
Calculate E for the cell as in the first problem. Then use nEocell*F = RT*ln K
A note: Long posts like this usually go unanswered. You will do well in the future to limit your posts to one problem per.