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Oxidation States of Tin

The elements of Group IV A exhibit two common oxidation states (+2 and +4) with the lower
oxidation state (ll) becoming increasingly stable as the group is descended. The relative stability
of the oxidation states is the result of two factors:
(a) The energy required to promote one of the paired s valence electrons on the group IV A
element to the empty p orbital decreases down the group.
ns2 np2 ns1 np3
(b) Bond strength as the group is descended, orbital overlap is less effective as the valence
orbitals become more diffuse resulting in longer and weaker covalent bonds.
For the first three group IV A elements the +IV oxidation state is predominant since the bond
energy term compensates for the required promotion energy. At tin, both factors are finely
balanced while for the lead the second factor is the dominant one.
In this experiment, tin (II) will be prepared by a metathetical reaction
Sn2+(aq) + 2I-(aq) SnI2(s)
while tin (IV) iodide is prepared by direct
Sn(s) + 2I2(aq) SnI4(s)

Reflux condenser

100 mL round bottom flask

Water bath

Melting point apparatus

0.8 g tin foil

1.6 g tin, granular

3.5 g iodine

25 mL of dichloromethane

Tin (IV) Iodide by direct reaction
Place 0.6g of tin granular and 2.4g of iodine crystals into a 100 mL round-bottom flask
containing a boiling stone equipped with a reflux condenser. Add 20 mL of dichloromethane
through the condenser. Gently heat the flask and contents so that mild reflux is maintained for
30-40 minutes and the violet colour of iodine vapour in the condenser disappears. Rapidly filter
the warm solution through a loose glass wool plug using a normal gravity funnel. Rinse the
reaction flask with 3 mL warm dichloromethane, pour through the same glass wool plug and
combine the dichloromethane filtrates.
Concentrate the dichloromethane to a volume of 5 10 mL (fume hood), cool the resulting
solution in an ice-water bath and collect the orange-red crystals of tin (IV) iodide. Wash with
two 2 mL portions of cold dichloromethane.

Tin (II) Iodide by metathesis
(To commence after refluxing begins in Part A)
Into a 100 mL beaker place 1.0g of powder zinc and 5 mL of distilled water. Add 1.0g of iodine
crystals and cool the beaker in an ice-water bath. Stir the reaction mixture with a glass rod. After
a few minutes a brown colour develops because of dissolved iodine. Continue cooling (the
reaction is exothermic) and stirring until all the zinc dissolves. At the end of the reaction some
unreacted zinc may remain but the solution become light yellow.
Filter the ZnI2 solution (through a plug of glass wool) into another 100 mL beaker. Rinse the
contents of the original beaker with 1 mL distilled water and transfer the washings (via the
glass wool plug) into the second beaker.
While the zinc-iodine reaction is in progress set up the preparation of the tin (II) chloride as
Add 0.8g of tin foil into a 50 mL beaker. Add 5 mL conc HCl and 1 mL 0.1M CuSO4 solution.
Heat the beaker and contents on a water bath until all the tin dissolves. Filter the tin (II) solution
(glass wool plug) and add it dropwise to the beaker containing the previously prepared ZnI2
solution. An orange yellow precipitate of SnI2 will be obtained. Cool in ice to complete

precipitation and collect the solid on a Buchner funnel. Calculate the % yield of the product and
determine its melting point.

Carry out the procedure in question 2 below before leaving the lab and clearly record your
observations in your note book!
1. Why is Tin (II) iodide a negligible product in the direct synthesis of tin (IV) iodide?
(4 marks)
2. To a mixed solution of FeCl3 and K3Fe(CN)6 add a freshly prepared solution of SnI2 and
explain your observations.
(5 marks)
3. Define the term metathetical reaction with the aid of balanced equations and an example
other than tin.
(6 marks)