E* = 3.03 V for F2(g) + 2 H+(AQ) + 2 e- -> 2 HF (aq), E* = 3.03 V
Find Ka of HF
the E* value for F2 + 2 e- -> 2 F- is 2.87 V.
If we want the cell to be favorable, we want a positive E*cell value right?
So why in the solutions manual do they do E*cell = 2.87 V - 3.03 V? = -0.16 V
(Why do they choose HF reaction to be the anode, and the 2F- reaction to be the cathode?)
Additionally, how do we find Ka after calculating K?
Textbook 6.57 Question about Favorability, choosing Cathode, anode
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Re: Textbook 6.57 Question about Favorability, choosing Cathode, anode
Normally if you are determining the cell potential of a Galvanic cell, you want the most positive cell potential. However, in this problem, you are not constructing a Galvanic cell; instead, you are simply trying to find Ka for HF.
The K that you find using the Nernst equation is for double the reaction you want. Therefore, to get K for the single reaction (dividing the overall reaction by 2), you need to take the square root of K (raise K to the 1/2 power).
The K that you find using the Nernst equation is for double the reaction you want. Therefore, to get K for the single reaction (dividing the overall reaction by 2), you need to take the square root of K (raise K to the 1/2 power).
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Re: Textbook 6.57 Question about Favorability, choosing Cathode, anode
Why doesn't the 3.03V become negative when the equation gets flipped?
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Re: Textbook 6.57 Question about Favorability, choosing Cathode, anode
FionaHunter21 wrote:Why doesn't the 3.03V become negative when the equation gets flipped?
I believe the 3.03V becomes negative.
E°cell = E°cathode - E°anode
-0.16V = +2.87V - 3.03V
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