Electrochemistry Concepts and Redox Reactions

Electrochemistry
 
homework
Chapter 18
Electrochemistry
AP Practice test
Oxidation- Reduction
Reactions
Redox or oxidation-reduction reactions are
reactions that involve a transfer of electrons.
O
xidation 
i
s the 
l
oss
 of electrons.
R
eduction 
i
s the 
g
ain
 of electrons.
(think of the charge, 
OIL RIG
)
So in the reaction
4 K + O
2
 
→ 4 K
+
  +  2 O
2-
Potassium get oxidized, oxygen get reduced
Oxidation States
Oxidation state is the theoretical charge
on all atoms if all bonds were ionic.
The sum of the oxidation states must be
equal to the charge of the ion or molecule.
Using oxidation states
 
In the reaction…
2 Na +2 H
2
O  
→2 NaOH + H
2
    0      +1 -2       +1 -2 +1   0
Note the changes
Sodium went from 0 to 1
2 of the hydrogen atoms went from +1 to 0
(the other two were unchanged)
Identification of Redox
Components.
Specify which of the following equations
represents oxidation-reduction reactions, and
indicate the oxidizing agent, the reducing agent,
the species being oxidized,  and the species
being reduced.
 
CH
4
(g)  +  H
2
O(g) 
 CO(g)  +  3H
2
(g)
   
2AgNO
3
(aq)  +  Cu(s) 
  Cu(NO
3
)
2
(aq)  +  2Ag(s)
2 H
+
(aq)  +  2CrO
4
2-
(aq) 
  Cr
2
O
7
2-
(aq)  +  H
2
O(l)
 
CH
4
(g)  +  H
2
O(g) 
 CO(g)  +  3H
2
(g)
-4 +1         +1 -2      +4 -2           0
C is oxidized, and H is reduced
C is reducing agent, H is oxidizing agent
2AgNO
3
(aq)  +  Cu(s) 
  Cu(NO
3
)
2
(aq)  +  2Ag(s)
 
+1 +5-2             0          +2  +5 -2                0
Ag is reduced, Cu is oxidized
Ag is oxidizing agent, Cu is reducing agent
Net Ionic
2Ag
+
(aq)  +  Cu(s) 
  Cu
2+
 (aq)  +  2Ag(s)
  +1              0            +2                  0
Ag is reduced, Cu is oxidized
 
2 H
+
(aq)  +  2CrO
4
2-
(aq) 
  Cr
2
O
7
2-
(aq)  +  H
2
O(l)
   +1             +6 -2                +6 -2              +1 -2
This is not a redox reaction
Half reactions
 
Ce
4+
 + Sn
2+
 
→ Ce
3+ 
+ Sn
4+
Half reactions
Ce
4+
 + e
-
 
→ Ce
3+
Sn
2+
 
→ 2e
- 
+ Sn
4+
Electrons lost must equal electrons gained!
2
 Ce
4+
 +
2
 e
-
 
2
 Ce
3+
Merge the two half reactions
2 Ce
4+
 + Sn
2+
 
→ 2 Ce
3+ 
+ Sn
4+
 
Redox reactions in acidic
solutions
It will be noted in the problem
Balance all elements except hydrogen and
oxygen.
Balance oxygen by adding H
2
O (which is
always prevalent in an acidic solution)
Balance hydrogen by adding H
+
Then balance the charge adding electrons and
proceed normally.
Example
 
In an acidic solution
Cr
2
O
7
 
2-
 + Cl
-
 
→ Cr
3+
 + Cl
2
Half reactions
Cr
2
O
7
 
2-
 
→ Cr
3+
Cl
-
 
→ Cl
2
Reduction side
 
Cr
2
O
7
 
2-
 
→ Cr
3+
Cr
2
O
7
 
2-
 
→ 2 Cr
3+
Cr
2
O
7
 
2-
 
→ 2 Cr
3+ 
+ 7 H
2
O
Cr
2
O
7
 
2-
 + 14 H
+
→ 2 Cr
3+ 
+ 7 H
2
O
Cr
2
O
7
 
2-
 + 14 H
+
+ 6 e
-
 →2Cr
3+
+7 H
2
O
Oxidation side
 
Cl
-
 
→ Cl
2
2 Cl
-
 
→ Cl
2
2 Cl
-
 
→ Cl
2 
+ 2 e
-
I have to equal 6 e
-
 so multiply by 3
6 Cl
-
 
→ 3 Cl
2 
+ 6 e
-
Combine my half reactions
 
Cr
2
O
7
 
2-
 + 14 H
+
+ 6 e
-
 → 2 Cr
3+ 
+ 7 H
2
O
6 Cl
-
 
3 Cl
2
 
+ 6 e
-
And you get
Cr
2
O
7
 
2-
+14 H
+
+
6Cl
-
→2Cr
3+
+
3 Cl
2
+7H
2
O
The electrons cancel out .
Example
 
In an acidic solution
MnO
4
- 
+ H
2
O
2
 
→ Mn
2+ 
 + O
2
Half reactions
MnO
4
- 
→ Mn
2+
H
2
O
2
 
→ O
2
Top Equation
 
MnO
4
- 
→ Mn
2+
MnO
4
- 
→ Mn
2+ 
+ 4 H
2
O
MnO
4
- 
+ 8 H
+
→ Mn
2+ 
+ 4 H
2
O
MnO
4
- 
+ 8 H
+
+ 5 e
-
→ Mn
2+ 
+ 4 H
2
O
Bottom Equation
 
H
2
O
2
 
→ O
2
H
2
O
2
 
→ O
2 
+ 2 H
+
H
2
O
2
 
→ O
2 
+ 2 H
+ 
+ 2 e
-
I need to equal 5 e
-
 so…
That won’t work…
2MnO
4
- 
+ 16 H
+
+ 10 e
-
→ 2 Mn
2+ 
+ 8 H
2
O
5 H
2
O
2
 
→ 5 O
2 
+ 10 H
+ 
+ 10 e
-
Add them together
 
2MnO
4
- 
+ 16 H
+
+ 10 e
-
→ 2 Mn
2+ 
+ 8 H
2
O
5 H
2
O
2
 
→ 5 O
2 
+ 10 H
+ 
+ 10 e
-
And you get
2 MnO
4
- 
+ 6 H
+
+ 5 H
2
O
2
   
→ 2 Mn
2+ 
+
 5 O
2 
+ 8 H
2
O
Notice the H
+ 
canceled out as well.
Balancing Redox Equations in a
basic solution
 
Look for the words basic or alkaline
Follow all rules for an acidic solution.
After you have completed the acidic
reaction add OH
-
 to each side to neutralize
any H
+
.
Combine OH
-
 and H
+
 to make H
2
O.
Cancel out any extra waters from both
sides of the equation.
Example
 
We will use the same equation as
before
In a basic solution
MnO
4
- 
+ H
2
O
2
 
→ Mn
2+ 
 + O
2
 
2 MnO
4
- 
+ 6 H
+
+ 5 H
2
O
2
    
→ 2 Mn
2+ 
+
 5 O
2 
+ 
8 H
2
O
Basic solution
 
Since this is a basic solution we can’t have
excess H
+
.
We will add OH
- 
to each side to neutralize
all H
+
2 MnO
4
- 
+ 6 H
+
+ 5 H
2
O
2
 + 
6OH
-
   
→2 Mn
2+ 
+
5 O
2 
+
8 H
2
O 
+ 
6OH
-
We added 6 OH
-
 because there were 6H
+
Cont.
 
H
+ 
+ OH
- 
→  H
2
O
Combine the hydroxide and hydrogen on the
reactant side to make water
2 MnO
4
- 
+ 
6 
H
2
O
 + 5 H
2
O
2
   
→ 2 Mn
2+
+
 5 O
2
+ 
8 H
2
O 
+ 6OH
-
Cancel out waters on both sides
2 MnO
4
- 
+ 5 H
2
O
2
   
→2 Mn
2+ 
+
 5 O
2 
+
2 H
2
O 
+6OH
-
Another example
 
In a basic solution
MnO
4 
 + SO
3
2-
→MnO
4 
2−
 + SO
4
2-
Half reactions
MnO
4 
 →  MnO
4 
2−
SO
3
2-
→  SO
4
2-
Half reactions
 
MnO
4 
 →  MnO
4 
2−
MnO
4 
-
 + e
-
 →  MnO
4 
2−
 
SO
3
2-
→  SO
4
2-
H
2
O + SO
3
2-
→  SO
4
2-
H
2
O + SO
3
2-
→  SO
4
2- 
+ 2 H
+
H
2
O + SO
3
2-
→  SO
4
2- 
+ 2 H
+ 
+2e
-
Double the top reaction
 
 
2 MnO
4 
-
 + 2 e
-
 →  2 MnO
4 
2−
H
2
O + SO
3
2-
→  SO
4
2- 
+ 2 H
+ 
+2e
-
Combine them
2 MnO
4 
-
 + H
2
O + SO
3
2-
   
→  2 MnO
4 
2− 
+SO
4
2- 
+ 2 H
+
Add OH
-
2 MnO
4 
-
 + H
2
O + SO
3
2- 
+ 2 OH
-
  
→ 2 MnO
4 
2−
+SO
4
2- 
+2 H
+
+2 OH
-
 
 
2 MnO
4 
-
 + H
2
O + SO
3
2- 
+ 2 OH
-
   
→  2 MnO
4 
2− 
+SO
4
2- 
+ 2 H
2
O
finishing
2 MnO
4 
-
 + SO
3
2- 
+ 2 OH
-
   
→  2 MnO
4 
2− 
+SO
4
2- 
+ H
2
O
 
Major Redox Points to
Remember.
Any redox reaction can be treated as the
sum of the
 
reduction and oxidation half-
reactions.
Mass (atoms) and charge are conserved in
each half-reaction.
Electrons lost in one half-reaction are
gained in the other.
Even though the half-reactions are
treated separately,
 
electron loss and
electron gain occur simultaneously.
Galvanic Cell
 
Galvanic cell
A 
galvanic cell
 is a device in which chemical
energy is changed to electrical energy.
A galvanic cell uses a 
thermodynanamically
favored or spontaneous
 redox reaction to
produce an electric current that can be
used to do work.  The system does work on
the surroundings.
A redox reaction involves the transfer of
electrons from the 
reducing agent
 to the
oxidizing agent
.
Oxidation v reduction
Oxidation.
* Involves a loss of
electrons.
 * Increase in
oxidation number.
 * “To get more
positive.”
 * Occurs at the
anode
 of a galvanic
cell.
An Ox
Reduction.
* Involves a gain of
electrons.
* Decrease in
oxidation number.
* “To get more
negative.”
* Occurs at the
cathode
 of a galvanic
cell.
Red Cat
Production of Current
 
Oxidation Reactions involve a transfer of
electrons.
Electric current is a 
movement of electrons
.
In order to produce a 
usable
 current, the
electrons must be forced across a set path
(circuit).
In order to accomplish this, an oxidizing agent
and something to oxidize must be separated
from a reducing agent with something to
reduce.
Pictures
 
Oxidation reduction reaction in
the same container will have
electrons transferring, but we
can’t harness them.
Separating the oxidation
reaction from the reduction
reaction, but connecting them
by a wire would allow only
electrons to flow.
 
Oxidation
 
Reduction
oxidation
reduction
Closer look
 
We now have 
excess electrons
 being formed in the
oxidizing solution and 
a need for electrons
 in the
reducing solution with a 
path
 for them to flow through.
However, if electrons did flow through the wire it would
cause a negative and positive solution to form.
Oxidation
Reduction
 
X 
  X
+
 + e-
 
X
+
 + e- →  X
That’s not possible
 
Or at least it would require a lot of energy.
A negative solution would theoretically be formed by
adding electrons, and a positive one by removing
electrons.
The negative solution would then repel the electrons
and stop them from flowing in, and a positive solution
would attract the electrons pulling them back where
they came from.
Making it so the charged solutions wouldn’t form.
In order for this to work, I would need a way for ions to
flow back and forth but keeping the solutions 
mostly
separated.
The Salt Bridge or the
Porous Disk.
These devices allow ion flow to occur
(circuit completion) 
without
 mixing
the solutions.  They are typically
made of sodium 
sulfate or potassium
nitrate
Closer look
Now electrons can flow across the wire from the
oxidation reaction to the reduction reaction.
As the oxidation reaction becomes positive, it removes
negative ions and adds positive ions to the salt bridge.
The reduction reaction does the reverse.
Oxidation
Reduction
X 
  X
+
 + e-
X
+
 + e- →  X
Salt Bridge
e
-
e
-
e
-
Closer look
Zooming in on the oxidizing side
This would make the salt bridge positive…
Oxidation side
e-
Salt Bridge
e
-
e
-
+ ion
+ ion
+ ion
+ ion
- ion
- ion
- ion
- ion
                                              Closer look
(Zooming in on the reducing side)
if the reverse wasn’t happening on this side.
Reducing side
e-
Salt Bridge
e
-
e
-
+ ion
+ ion
+ ion
+ ion
- ion
- ion
- ion
- ion
Close up of salt bridge
The ions keep flowing in the salt bridge to keep
everything neutral.
Electrons do also travel across the salt bridge.
This decreases the cell’s effectiveness.
+ ion
+ ion
+ ion
- ion
- ion
- ion
+ ion
+ ion
+ ion
- ion
- ion
- ion
Electrochemical cell
This is the basic unit of a battery.
It is also called a galvanic cell, batteries have
two or more galvanic cells linked together.
Electrochemical cells always have two
terminals.
The terminal where oxidation occurs is called
the 
anode
.
The terminal where reduction occurs is
called the 
cathode
.
Galvanic Cell
 
Voltaic Cell: Anode Reaction
At the anode, the metal at the terminal is losing electrons
going from metallic state to an aqueous state.
Over time the anode loses mass due to this.
Zn(s)
Zn(s)
Zn
2+
 (aq)
Voltaic Cell: Cathode Reaction
At the Cathode, the metal at the terminal is gaining electrons
going from aqueous to a metallic state.
Over time the cathode gains mass due to this.
Ag(s)
Ag(s)
Ag
+
 (aq)
Ag
+
 (aq)
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Explore the fundamentals of electrochemistry, oxidation-reduction reactions, and identification of redox components. Learn about oxidation states, electron transfer, and half-reactions. Dive into examples and visual aids to grasp the concepts easily.

  • Electrochemistry
  • Redox reactions
  • Oxidation states
  • Half-reactions
  • Chemistry

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  1. Electrochemistry

  2. homework Chapter 18 Electrochemistry AP Practice test

  3. Oxidation-Reduction Reactions Redox or oxidation-reduction reactions are reactions that involve a transfer of electrons. Oxidation is the loss of electrons. Reduction is the gain of electrons. (think of the charge, OIL RIG) So in the reaction 4 K + O2 4 K++ 2 O2- Potassium get oxidized, oxygen get reduced

  4. Oxidation States Oxidation state is the theoretical charge on all atoms if all bonds were ionic. The sum of the oxidation states must be equal to the charge of the ion or molecule.

  5. Using oxidation states In the reaction 2 Na +2 H2O 2 NaOH + H2 0 +1 -2 +1 -2 +1 0 Note the changes Sodium went from 0 to 1 2 of the hydrogen atoms went from +1 to 0 (the other two were unchanged)

  6. Identification of Redox Components. Specify which of the following equations represents oxidation-reduction reactions, and indicate the oxidizing agent, the reducing agent, the species being oxidized, and the species being reduced. CH4(g) + H2O(g) CO(g) + 3H2(g) 2AgNO3(aq) + Cu(s) Cu(NO3)2(aq) + 2Ag(s) 2 H+(aq) + 2CrO42-(aq) Cr2O72-(aq) + H2O(l)

  7. CH4(g) + H2O(g) CO(g) + 3H2(g) -4 +1 +1 -2 +4 -2 0 C is oxidized, and H is reduced C is reducing agent, H is oxidizing agent 2AgNO3(aq) + Cu(s) Cu(NO3)2(aq) + 2Ag(s) +1 +5-2 0 +2 +5 -2 0 Ag is reduced, Cu is oxidized Ag is oxidizing agent, Cu is reducing agent Net Ionic 2Ag+(aq) + Cu(s) Cu2+(aq) + 2Ag(s) +1 0 +2 Ag is reduced, Cu is oxidized 0 2 H+(aq) + 2CrO42-(aq) Cr2O72-(aq) + H2O(l) +1 +6 -2 +6 -2 +1 -2 This is not a redox reaction

  8. Half reactions Ce4++ Sn2+ Ce3+ + Sn4+ Half reactions Ce4++ e- Ce3+ Sn2+ 2e-+ Sn4+ Electrons lost must equal electrons gained! 2 Ce4++2 e- 2 Ce3+ Merge the two half reactions 2 Ce4++ Sn2+ 2 Ce3+ + Sn4+

  9. Redox reactions in acidic solutions It will be noted in the problem Balance all elements except hydrogen and oxygen. Balance oxygen by adding H2O (which is always prevalent in an acidic solution) Balance hydrogen by adding H+ Then balance the charge adding electrons and proceed normally.

  10. Example In an acidic solution Cr2O72-+ Cl- Cr3++ Cl2 Half reactions Cr2O72- Cr3+ Cl- Cl2

  11. Reduction side Cr2O72- Cr3+ Cr2O72- 2 Cr3+ Cr2O72- 2 Cr3+ + 7 H2O Cr2O72-+ 14 H+ 2 Cr3+ + 7 H2O Cr2O72-+ 14 H++ 6 e- 2Cr3++7 H2O

  12. Oxidation side Cl- Cl2 2 Cl- Cl2 2 Cl- Cl2 + 2 e- I have to equal 6 e-so multiply by 3 6 Cl- 3 Cl2 + 6 e-

  13. Combine my half reactions Cr2O72-+ 14 H++ 6 e- 2 Cr3+ + 7 H2O 6 Cl- 3 Cl2+ 6 e- And you get Cr2O72-+14 H++6Cl- 2Cr3++3 Cl2+7H2O The electrons cancel out .

  14. Example In an acidic solution MnO4-+ H2O2 Mn2+ + O2 Half reactions MnO4- Mn2+ H2O2 O2

  15. Top Equation MnO4- Mn2+ MnO4- Mn2+ + 4 H2O MnO4-+ 8 H+ Mn2+ + 4 H2O MnO4-+ 8 H++ 5 e- Mn2+ + 4 H2O

  16. Bottom Equation H2O2 O2 H2O2 O2 + 2 H+ H2O2 O2 + 2 H+ + 2 e- I need to equal 5 e-so That won t work 2MnO4-+ 16 H++ 10 e- 2 Mn2+ + 8 H2O 5 H2O2 5 O2 + 10 H+ + 10 e-

  17. Add them together 2MnO4-+ 16 H++ 10 e- 2 Mn2+ + 8 H2O 5 H2O2 5 O2 + 10 H+ + 10 e- And you get 2 MnO4-+ 6 H++ 5 H2O2 2 Mn2+ + 5 O2 + 8 H2O Notice the H+ canceled out as well.

  18. Balancing Redox Equations in a basic solution Look for the words basic or alkaline Follow all rules for an acidic solution. After you have completed the acidic reaction add OH-to each side to neutralize any H+. Combine OH-and H+to make H2O. Cancel out any extra waters from both sides of the equation.

  19. Example We will use the same equation as before In a basic solution MnO4-+ H2O2 Mn2+ + O2 2 MnO4-+ 6 H++ 5 H2O2 2 Mn2+ + 5 O2 + 8 H2O

  20. Basic solution Since this is a basic solution we can t have excess H+. We will add OH-to each side to neutralize all H+ 2 MnO4-+ 6 H++ 5 H2O2+ 6OH- 2 Mn2+ +5 O2 +8 H2O + 6OH- We added 6 OH-because there were 6H+

  21. Cont. H+ + OH- H2O Combine the hydroxide and hydrogen on the reactant side to make water 2 MnO4-+ 6 H2O + 5 H2O2 2 Mn2++ 5 O2+ 8 H2O + 6OH- Cancel out waters on both sides 2 MnO4-+ 5 H2O2 2 Mn2+ + 5 O2 +2 H2O +6OH-

  22. Another example In a basic solution MnO4 + SO32- MnO4 2 + SO42- Half reactions MnO4 MnO4 2 SO32- SO42-

  23. Half reactions MnO4 MnO4 2 MnO4 -+ e- MnO4 2 SO32- SO42- H2O + SO32- SO42- H2O + SO32- SO42-+ 2 H+ H2O + SO32- SO42-+ 2 H+ +2e- Double the top reaction

  24. 2 MnO4 -+ 2 e- 2 MnO4 2 H2O + SO32- SO42-+ 2 H+ +2e- Combine them 2 MnO4 -+ H2O + SO32- 2 MnO4 2 +SO42-+ 2 H+ Add OH- 2 MnO4 -+ H2O + SO32-+ 2 OH- 2 MnO4 2 +SO42-+2 H++2 OH-

  25. 2 MnO4 -+ H2O + SO32-+ 2 OH- 2 MnO4 2 +SO42-+ 2 H2O finishing 2 MnO4 -+ SO32-+ 2 OH- 2 MnO4 2 +SO42-+ H2O

  26. Major Redox Points to Remember. Any redox reaction can be treated as the sum of the reduction and oxidation half- reactions. Mass (atoms) and charge are conserved in each half-reaction. Electrons lost in one half-reaction are gained in the other. Even though the half-reactions are treated separately, electron loss and electron gain occur simultaneously.

  27. Galvanic Cell

  28. Galvanic cell A galvanic cell is a device in which chemical energy is changed to electrical energy. A galvanic cell uses a thermodynanamically favored or spontaneous redox reaction to produce an electric current that can be used to do work. The system does work on the surroundings. A redox reaction involves the transfer of electrons from the reducing agent to the oxidizing agent.

  29. Oxidation v reduction Oxidation. * Involves a loss of electrons. * Increase in oxidation number. * To get more positive. * Occurs at the anode of a galvanic cell. An Ox Reduction. * Involves a gain of electrons. * Decrease in oxidation number. * To get more negative. * Occurs at the cathode of a galvanic cell. Red Cat

  30. Production of Current Oxidation Reactions involve a transfer of electrons. Electric current is a movement of electrons. In order to produce a usable current, the electrons must be forced across a set path (circuit). In order to accomplish this, an oxidizing agent and something to oxidize must be separated from a reducing agent with something to reduce.

  31. Pictures Oxidation reduction reaction in the same container will have electrons transferring, but we can t harness them. Separating the oxidation reaction from the reduction reaction, but connecting them by a wire would allow only electrons to flow. oxidation reduction Oxidation Reduction

  32. Closer look X X+ + e- X+ + e- X Oxidation Reduction We now have excess electrons being formed in the oxidizing solution and a need for electrons in the reducing solution with a path for them to flow through. However, if electrons did flow through the wire it would cause a negative and positive solution to form.

  33. Thats not possible Or at least it would require a lot of energy. A negative solution would theoretically be formed by adding electrons, and a positive one by removing electrons. The negative solution would then repel the electrons and stop them from flowing in, and a positive solution would attract the electrons pulling them back where they came from. Making it so the charged solutions wouldn t form. In order for this to work, I would need a way for ions to flow back and forth but keeping the solutions mostly separated.

  34. The Salt Bridge or the Porous Disk. These devices allow ion flow to occur (circuit completion) without mixing the solutions. They are typically made of sodium sulfate or potassium nitrate

  35. Closer look e- e- e- Salt Bridge X X+ + e- X+ + e- X Oxidation Reduction Now electrons can flow across the wire from the oxidation reaction to the reduction reaction. As the oxidation reaction becomes positive, it removes negative ions and adds positive ions to the salt bridge. The reduction reaction does the reverse.

  36. e- Closer look e- Salt Bridge - ion + ion Oxidation side e- + ion - ion - ion + ion + ion - ion Zooming in on the oxidizing side This would make the salt bridge positive

  37. e- Closer look e- Salt Bridge - ion + ion - ion e- + ion - ion Reducing side + ion - ion + ion (Zooming in on the reducing side) if the reverse wasn t happening on this side.

  38. Close up of salt bridge + ion + ion + ion - ion - ion - ion - ion - ion + ion + ion + ion - ion The ions keep flowing in the salt bridge to keep everything neutral. Electrons do also travel across the salt bridge. This decreases the cell s effectiveness.

  39. Electrochemical cell This is the basic unit of a battery. It is also called a galvanic cell, batteries have two or more galvanic cells linked together. Electrochemical cells always have two terminals. The terminal where oxidation occurs is called the anode. The terminal where reduction occurs is called the cathode.

  40. Galvanic Cell

  41. Voltaic Cell: Anode Reaction At the anode, the metal at the terminal is losing electrons going from metallic state to an aqueous state. Over time the anode loses mass due to this. Zn(s) Zn(s) Zn2+ (aq)

  42. Voltaic Cell: Cathode Reaction At the Cathode, the metal at the terminal is gaining electrons going from aqueous to a metallic state. Over time the cathode gains mass due to this. Ag(s) Ag(s) Ag+ (aq) Ag+ (aq)

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