All Questions
Tagged with equilibrium electrochemistry
47
questions
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Iodine/iodide electrochemistry help
I have an electrochemistry experiment with iodine in solution.
I am initially wanting to quantify the iodide in solution and extrapolate the concentration of I2(aq) and I3-(aq) in solution from this ...
0
votes
1
answer
121
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How does cell potential change with temperature for positive enthalpy and negative entropy?
A recent United States National Chemistry Olympiad question asked:
A certain voltaic cell has a standard cell potential that increases with increasing temperature. Which best explains this ...
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-2
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1
answer
122
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Inconsistency in between Nernst Equation and Gibbs Free Energy Equation [closed]
Part 1 - Derivation of the Gibbs Free Energy Equation: [copied from this]
Using the fundamental equations for the state function (and its natural variables):
\begin{align}
\mathrm{d}G &= -S\...
4
votes
2
answers
800
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Acid dissociation constant from conductometric data
$\ce{0.007 M}$ aq. solution of anilinium hydrochloride had molar conductivity equal to $\pu{119.4 S cm2 mol-1}$, which became $\pu{103 S cm2 mol-1}$ when a few drops of aniline were added to the ...
- 828
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1
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70
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Can an electrode run out of the active species?
I have a background in solid state physics but am new to electrochemistry. I have been following the example of a physical chemistry (Mortimer) book that looks an electrochemical cell with a hydrogen ...
- 9
1
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1
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757
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Why is the theoretical value of the electrode potential different to the experimental value for Cu and Al for a galvanic cell by using Nernst equation
I've construct a galvanic cell with the Al strip putting in the Aluminum nitrate solution and Cu strip putting in the CuSO4 solution. KNO3 is used as the salt bridge in this experiment. The question ...
- 11
0
votes
1
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559
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Degree of dissociation and conductance
My book says ratio of molar conductance at a given concentration of solute and molar concentration at infinite dilution is equal to degree of dissociation for weak electrolytes.
I understand it ...
- 1
2
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1
answer
389
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Electrode potential for saturated silver carbonate solution
An electrochemical cell is set up to measure the electrode potential $E(\ce{Ag^+}/\ce{Ag})$ using the saturated $\ce{Ag2CO3(aq)}$ solution $(K_\mathrm{sp}(\ce{Ag2CO3(aq)},\pu{25 °C}) = \pu{6.3E-12})$ ...
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-3
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1
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70
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Voltaic cell equilibrium confusion
In a voltaic cell, taking one with $\ce{Zn}$ and $\ce{Cu }$ electrodes for an example, an EMF is formed because the equilibria at the $\ce{Zn}$ electrode is shifted more towards the $\ce{Zn^2+ + 2e-}$ ...
- 126
2
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0
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165
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How do the assumptions of the Nernst equation impact its accuracy?
I was just wondering what impact the assumption that the equilibrium membrane potential for an ion is dependent on just the ion itself (if it is the only thing that is permeable). For instance, if I ...
- 21
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1
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170
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Calculating Gibbs free energy change when the state of ions is unknown
Problem
Calculate $\Delta G^\circ$ for the following reaction:
$$\ce{Zn(s) + Ag2O(s) + H2O(l) -> Zn^{+2}(aq) + 2Ag(s) + 2OH-(aq)}$$
Given $E^\circ_{\ce{Ag+/Ag}} = \pu{0.80 V}$, $E^\circ_{\ce{Zn^{+...
- 1,817
1
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0
answers
1k
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Why does the reaction between copper(II) ion and iodide ion proceed even though the E_cell of the set up is negative?
(iii) Another example of a reaction that does not agree with the theoretical prediction is the reaction between $\mathrm{Cu}^{2+}$ and $\mathrm{I}^{-}$ according to the equation below.
$$
2 \mathrm{Cu}...
2
votes
1
answer
313
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Relation between standard silver-silver chloride electrode potential and solubility product of silver chloride
I learned that $E^\circ_\ce{Cl^-|Ag,AgCl}, E^\circ_\ce{Ag^+|Ag}$ and $K_\mathrm{sp}$ of $\ce{AgCl}$ are related as
$$\boxed{E^\circ_\ce{Cl^-|Ag,AgCl} = E^\circ_\ce{Ag^+|Ag} + \frac{RT}{F}\ln K_\mathrm{...
- 750
2
votes
1
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223
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Intuition for relation between electrode potential and reaction quotient
Consider the following reaction in a galvanic cell: $$\ce{X(s) + Y+(aq) -> Y(s) + X+(aq)}$$
According to the Nernst equation, $$E =E_\circ - \dfrac{RT}{F}\ln\left(\dfrac{\ce{[X+]}} {\ce{[Y+] }} \...
- 750
1
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1
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220
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Why is "activity" of gaseous component equal to its partial pressure but that of aqueous component its concentration?
While solving an electrochemistry problem I had to calculate the reaction quotient of this reaction:
$$\ce{2Fe(s) + 4H+(aq) + O2(g) -> 2Fe^{2+} (aq) + 2H2O (l)}$$
It turns out to be: $$\ce{Q=\dfrac{...
- 750