AQA A Level Chemistry

Revision Notes

6.2.5 Variable Oxidation States

Variable Oxidation States

  • The table below shows the most common oxidation states of a few transition metals

Oxidation states of transition elements table

Oxidation states of transition elements table, downloadable AS & A Level Chemistry revision notes

  • When transition elements forms ions they lose electrons from the 4s subshell first
  • This is because when the orbitals are occupied, the repulsion between electrons pushes the 4s into a higher energy state so that it now becomes slightly higher in energy than the 3d subshell
    • The 4s is now the outer shell and loses electrons first
  • The loss of the 4s electrons means that +2 is common oxidation state in transition metals
  • The reason why the transition metals have variable oxidation states all comes down to energy

Successive IE for Ti and V, downloadable AS & A Level Biology revision notes

Ionisation energies for the removal of successive electrons in titanium and vanadium

  • We can see from the graph that the first few ionisation energies are relatively small and relatively close together
  • This means that the energy difference associated with removing a small number of electrons enables transition metals to vary their oxidation state with ease

Redox Potential & Oxidation State

Influence of pH

  • The redox potential for a transition metal ion changing from a higher to a lower oxidation state is influenced by pH and by the ligand
  • When aqueous transition metal ions undergo a change in oxidation state, the reactions frequently involve hydrogen ions
  • By analysing the reaction equations we can see the redox processes taking place
  • The reduction of manganese in the manganate(VII) ion takes place readily in acidic solutions

MnO4 (aq) + 8H+ (aq) + 5e ⇌  Mn2+ (aq) + 4H2O (l)      E = +1.51 V  

  • The manganese changes from +7 to +2
  • The positive value of E indicates the equilibrium position is well over to the right
  • An excess of acid drops the pH and provides the hydrogen ions to ensure this reaction usually goes to completion
  • However, in a neutral solution the reduction is limited to the +4 oxidation state for the manganese

MnO4 (aq) + 2H2O (l) + 3e ⇌  MnO2 (s) + 4OH (aq)   E = +0.59 V  

  • Notice that the value of Eꝋ  has changed as a result of changing the pH of the solution

Changing the ligand

  • Changing the ligand also influences the redox potential
  • If you compare the aqueous nickel(II) ion with the hexaamminenickel(II) ion, the Ebecomes more negative when ammonia ligands replace water ligands

[Ni(H2O)6]2+ (aq) + 2e ⇌ Ni(s) + 6H2O (l)           E = -0.26

[Ni(NH3)6]2+ (aq) + 2e  ⇌  Ni(s) + 6NH3 (aq)    E = -0.49

  • Ammonia is a stronger ligand than water meaning that it binds better to the nickel(II) ion
  • The position of the second equilibrium is slightly more to the left than the first one (hence the more negative Evalue)

Oxidation states of Vanadium

  • The variation in oxidation states of transition metal ions is illustrated by the reaction of zinc with ammonium vanadate(V) (also known as ammonium metavanadate) under acidic conditions
  • Vanadium had four common oxidation states, from +2 to +5
  • Zinc is a reducing agent that is capable to reducing vanadium(V) to vanadium(II) in a sequence of steps accompanied by vibrant colour changes

Colours of vanadium, downloadable AS & A Level Biology revision notes

The reducing of vanadate(V) ions by zinc in acidic conditions is one of the most colourful reactions in chemistry

The colours of the different ions of vanadium are:

Vanadium ions and oxidation states table

Vanadium oxidation states Table, downloadable AS & A Level Biology revision notes

  • The first step in the reduction

2VO2+ (aq) + 4H+(aq) + Zn(s)  →   2VO2+ (aq) + 2H2O(l) + Zn2+ (aq)

  • The second step:

2VO2+ (aq) + 4H+(aq) + Zn(s)  →   2V3+ (aq) + 2H2O(l) + Zn2+ (aq)

  • The third step:

2V3+ (aq) + Zn(s)  →  2V2+ (aq) + Zn2+ (aq)

  • By carefully selecting suitable reducing agents you can stop the reduction of vanadium(V) at different states

Worked Example

Use the table of redox potentials to deduce the final oxidation state when a) tin and b) thiosulfate ions are used to reduce vanadium(V).

6.2.5 Worked Example 1, downloadable AS & A Level Chemistry revision notes

Answer

a) The reaction with tin:

    • Vanadium(V) is present as the ion VO2+ 
    • For a feasible reaction to take place Ecell (or the emf) must be positive
    • To act as a reducing agent tin, Sn , must provide electrons and the half equation will go backwards

2Sn  ⇌   Sn2+  + 2e

    • For this to be the case the tin half reaction potential must be more negative than the reaction containing the vanadium species
    • Only a reaction from vanadium(V) to vanadium(III) will give a positive emf

4VO2+  + 4H+ + Sn ⇌   2VO2+  + 2H2O  + Sn2+   Ecell = 1.00-(-0.14) = +1.14 V                                              

2VO2+  + 4H+ +  Sn   ⇌  2V3+ + 2H2O + Sn2+      Ecell = 0.34-(-0.14) = +0.48 V  

2V3+ + Sn ⇌  2V2+ + Sn2+                                           Ecell = -0.26-(-0.14) = -0.12 V  

Therefore the final oxidation state is +3 (as the final Ecell is -0.12 V which is negative meaning this reaction is not feasible) 

b) The reaction with thiosulfate ions

    • To act as a reducing agent thiosulfate ions, S2O32- , must provide electrons and the half equation will go backwards

2S2O32-  ⇌ S4O62- (aq) + 2e

    • For this to be the case the thiosulfate half reaction potential must be more negative than the reaction containing the vanadium species
    • Only a reaction from vanadium(V) to vanadium(IV) will give a positive emf

4VO2+  + 4H+ + 2S2O32- ⇌   2VO2+  + 2H2O  + S4O62-   Ecell = 1.00-0.47 = +0.53 V                                              

2VO2+  + 4H+ + 2S2O32-   ⇌  2V3+ + 2H2O + S4O62-      Ecell =  0.34-0.47 = -0.13 V  

2V3+ + 2S2O32- ⇌  2V2+ + S4O62-                                          Ecell = -0.26-0.47 =   -0.73 V  

The final oxidation state is therefore +4

Reduction of Tollens' Reagent

  • Tollens’ reagent contains the transition metal complex ion called diamminesilver(I), [Ag(NH3)2]+
  • It is not stable in solution so it prepared when needed by adding sodium hydroxide solution to silver nitrate solution followed concentrated ammonia solution
  • The reaction briefly produces a brown precipitate which quickly re-dissolves to form a colourless solution containing the diamminesilver(I) ion
  • Tollens’ reagent is used to distinguish between aldehydes and ketones, but it can also be used to detect reducing sugars such as glucose
  • A few drops of an aldehyde are warmed with Tollens’ reagent in a water bath

Carbonyl Compounds Tollens Reagent, downloadable AS & A Level Chemistry revision notes

Testing an aldehyde with Tollens’ reagent

  • Although aldehydes and ketones are very similar chemically, aldehydes are reducing agents and can reduce the silver ion to silver metal
  • The result is a striking silver mirror coating on the inside of the test tube, hence it is known as the ‘silver mirror’ test
  • The equation for the reaction is

[Ag(NH3)2]+       +    e        → Ag (s)   +      2NH3 (aq)  

  • Apart from its usefulness in chemistry this reaction was used in the past to create the coating on mirrors with silver
Close

Join Save My Exams

Download all our Revision Notes as PDFs

Try a Free Sample of our revision notes as a printable PDF.

Join Now
Already a member?
Go to Top