Page 354 - General Knowledge
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GENERAL KNOWLEDGE 2019
Aqueous solutions of salts that are products of strong acidic-weak base reactions are acidic.
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The Cations react with water and increases [H 3O ] in solutions.
Salts of Weak Acid-Weak Base Reactions: such as NH 4C 2H 3O 2, NH 4CN, NH 4NO 2, etc.
Solutions of salts that are products of weak acid-weak base reactions can be neutral, acidic,
or basic, depending on the relative magnitude of the K a of the weak acid and the K b of the
weak base.
5. ELECTROCHEMISTRY
A branch of chemistry that deals with the exploitation of spontaneous oxidation-reduction
reactions to obtain electrical energy and the use of electrical energy to drive nonspontaneous
reactions important in the industrial extraction of certain elements.
Electrode potentials and their measurements
One of the most common redox reactions is that which occurs when metals are immersed
into solutions of dissimilar metal ions is the single replacement reaction.
In other cases, mixing ions (in the presence of acid) leads to more complicated redox
reactions (recall the iodometric titration in the fall).
Regardless of complexity, some metals and ions are more easily reduced than others.
This difference in affinity for electrons drives chemical reactions.
The ease of oxidation, or the more accepted ease of reduction, is known as the Standard
Electrode Potential.
It is measured in volts which have the units, Joules/coulomb.
It is more a theoretical idea than anything functional. It is a half-cell represents the "half
reaction" from balancing redox reactions last fall and "half" of a reaction cannot occur.
Each metal will have a unique equilibrium with its ions that will result in a slight positive or
negative charge build-up on the electrode.
This tendency cannot be measured directly but can be measured by connecting different
half-cells to each other.
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Electrons will flow from the electrode of higher e density to the electrode of lower e density
(akin to electrons "diffusing").
To measure the difference in potential we connect two half-cells by joining the electrodes
with a wire and the cells to each other with a salt bridge to maintain electro-neutrality.
As ions related to the electrode enter or leave the solution, spectator ions in the salt bridge
migrate into the solutions to maintain charge balance.
The two half-cells, external electron circuit and the salt bridge is an Electrochemical Cell.
The voltage is the potential difference between the two half-cells and is called the
electromotive force (emf) or the cell potential.
Galvanic and Electrolytic Cells
2+
-
At anode Cd is oxidized, Cd goes into solution, balanced by NO 3 coming from salt bridge
2+
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At cathode, Ni is reduced, comes out of solution as Ni, balanced by NO 3 going into the
bridge
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Negative charge as NO 3 flows through bridge from cathode (Ni) to anode (Cd)
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Negative charge as e flows through wire from anode (Cd) to cathode (Ni)
2+
2+
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Conversely, Na moves through bridge to Ni side (Ni consumed) from Cd side (Cd
produced).
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