Reduction reactions
reactants gain electrons
Oxidation reactions
reactants lose electrons
Lavoisier’s explanation of redox reactions
Oxidation = gain of oxygen, loss of hydrogen
Reduction = loss of oxygen, gain of hydrogen
Oxidation states
measure of the electron control/possession an atom has relative to the atom in the pure element state
assigned to each atom to keep track of electrons
signifies electron control gained or lost
Oxidation state of atoms in free element form
ZERO
Oxidation state of simple ions
same as the charge on the ion
Oxidation states of all atoms in a neutral compound add to __
ZERO
Oxidation states of all atoms in a polyatomic ion add to ______
the charge of the polyatomic ion
usual oxidation state for an element is
the same as the charge on its most common ion (many exceptions exist; most main group non metals, elements at bottom of group 14, and transition metals have variable oxidation states)
Li, Na, K usual oxidation state
+1
Mg, Ca usual oxidation state
+2
F usual oxidation state
-1
O usual oxidation state (and exceptions)
-2, in peroxides (H2O2) it is -1, in OF2 it is +2
H usual oxidation state (and exceptions)
+1, -1 in metal hydrides such as NaH
Cl usual oxidation state
-1, different when combined with O or F
PRACTISE :) Assign oxidation states to each atom
(Co(NH3)6)3+
Co: +3
N: -3
H: +1
Greater oxidation states indicate…
the more the atom has lost control over electrons, the more oxidized it is
More negative oxidation states indicate…
the more the atom gains control over electrons, the more reduced it is
Half reactions
Splits overall redox into distinct reduction and oxidation reactions
The two half reactions occur at the same time
They must have an equal number of electrons on both half-reactions to cancel when added together
Steps for constructing equations with half reactions
Assign oxidation states to determine which atoms are being oxidized and which are being reduced
Write half equations
Balance atoms other than H and O
Balance each half-reaction for O by adding H2O
Balance the H by adding H+
Balance the charges by adding electrons to side with positive charge
Equalize the number of electrons by multiplying half reactions appropriately
Add two half-reactions together, cancelling same on both sides
Oxidizing agent
the reactant that accepts electrons, as it brings about oxidation of other reactant
It itself reduces
Reducing agent
The reactant that supplies electrons, as it brings about reduction in the other reactanbt
It itself oxidizes
Explanation of the activity series of metals in relation to reducing power
By comparing displacement reactions between different combinations of metals and their ions, we build up a list of relative strengths of metals as reducing agents
Allows us to predict if a particular redox reaction is feasible
More reactive metals are stronger reducing agents, meaning they oxidize most readily
Will this reaction occur?
ZnCl2 + 2Ag → 2AsCl + Zn
No twink! silver is a weaker reducing agent
STUDY BREAK
go make a snack or a drink
Explanation of the activity series of halogens in relation to oxidizing power
More reactive halogens (high EN) most readily become reduced and are strong oxidizing agents
Equation of redox titration using acidified potassium permanganate to analyze iron
5Fe2+ + MnO4- + 8H+ → 5Fe3+ + Mn2+ + 4H2O
(the K is not considered)
Description of Iodine - Thiosulfate redox titration
Uses an oxidant to react with excess iodine ions to form iodine
2I- + Oxidizing agent → I2 + Reduced product
The liberated iodine, I2 is then titrated with sodium thiosulfate (Na2S2O3) using starch as an indicator
2Na2SO4 + I2 → 2NaI + Na2S4O6
Biological oxygen demand
measure of the degree of pollution of a body of water
the amount of oxygen used to decompose organic matter over a specified time period (usually 5 days)
Ratio of water to S2O32- in the Winkler method
1 mol: 4 mol
Description of Galvanic/Voltaic cells
Generate electricity from spontaneous redox reactions —converts chemical energy to electrical energy
Half reactions are separated into half-cells, and electrons are allowed to flower between them through an external circuit
In a half cell, a strip of metal is placed into a solution of its own ions
Electrode potential in Galvanic cells
charge separation formed between the metal and its ions in solution
The connection between half cells
an external wire allows electrons to spontaneously flow from the half cell where oxidation is occurring ANODE (eg. zinc) to half cell where reduction is occurring CATHODE (eg. copper)
a salt bridge completes the circuit: a glass tube or strip of absorptive paper containing aqueous solutions of ions. Allows for the free flow of ions between half cells and neutralizes/balances charge
KNO3 often used
Cell diagram convention of a zinc and copper galvanic cell
Zn(s) | Zn2+(aq) || Cu2+(aq) | Cu(s)
→ the direction of electron flow →
Description of electrolytic cells
an external source of electricity drives a non-spontaneous redox reaction
Electrolytic cells use an external source of electrical energy to bring about a redox reaction (ie. converts electrical energy to chemical energy
Electrodes are immersed in an electrolyte (solution of ionic compounds) and connected to a power supply, they are described as inert, but must not touch
Electric wires connect the electrodes to the power supply
Describe the electrolysis of a molten salt
When the electrolyte is a molten salt, the only ions present are those from the compound itself as there is no solvent
One ion migrates to each electrode