CCEA ADVANCED SUBSIDIARY
CHEMISTRY
2.9 Group II (magnesium to barium, as
indicated)
Trends within the group limited to colour, physical state,
melting points, atomic and ionic radii, first ionisation energy.
Group trends
|
|
Magnesium |
Calcium |
Strontium |
Barium |
|
Colour |
Silver |
Silver/ grey |
Silver |
Silver |
|
State at Ro |
solid |
solid |
solid |
solid |
|
Melting pt. oC |
650 |
850 |
768 |
714 |
|
Boiling pt. oC |
1100 |
1487 |
1380 |
1640 |
|
Metallic radius nm. |
0.160 |
0.197 |
0.215 |
0.224 |
|
Ionic radius M2+ nm. |
0.072 |
0.100 |
0.113 |
0.136 |
|
First ionisation energy kJ mol-1 |
738 |
590 |
550 |
503 |
Group II comprises a series of reactive metals with low densities. They are a silver-grey colour when clean but tarnish quickly in air due to the formation of the metal oxide.
Where possible, the following should be investigated
practically.
Chemical trends, including combustion, reaction with water and
dilute acids. Flame colorations produced by the metal ions. Basic nature of
oxides. Thermal stability of carbonates and hydroxides related to cation size
and lattice energies. Solubility trends of sulphates and hydroxides explained
only by enthalpy considerations.
Combustion
They burn in air or oxygen to form the solid white oxide MO.
2M (s) + O2 (g) 2MO (s)
The metal oxides are ionic compounds
containing the metal cation and oxide ion (M2+O2-).
The group II oxides all react with water to
form hydroxides
MO (s) + H2O (l) M(OH)2
(aq)
The metal hydroxides dissolve in water to
give OH- (aq) and are thus basic.
M(OH) (s) + aq M2+
(aq) +
2OH- (aq)
The metals react vigorously with water
giving an alkaline solution of the metal hydroxide and hydrogen gas.
M (s) + 2H2O(l) M(OH)2 (aq) + H2
(g)
Reactivity increases down the group due to
the increasing ease of losing electrons.
Magnesium reacts very slowly with water,
but quickly with steam forming MgO.
Mg (s) + H2O (g) MgO
(s) + H2 (g)
Group II metals react even more vigorously
with acids than with water forming the metal salt and hydrogen.
M (s) + 2H+ (aq) M2+ (aq) + H2
(g)
Again reactivity increases down the Group
as the outer shell electrons are lost more readily.
Some Group II metals produce characteristic
flame colours when compounds containing their ions are heated. These colours
can be used to identify their presence in unknown compounds (as well as making
colourful firework displays !!).
|
METAL |
FLAME COLOUR |
|
Calcium |
Brick red |
|
Strontium |
Crimson |
|
Barium |
Apple green |
The stability of a
salt depends on two factors.
·
The greater
the charges on the ions, the greater the attraction between them, and the
greater the lattice enthalpy.
·
The smaller
the ions, the more closely they can approach each other in the lattice, and the
greater the lattice energy.
In group II
carbonates we might expect that they would become easier to decompose as the
group is descended.
In fact the ease
of decomposition decreases down the group and this is related to the polarising
power of the metal cation.
An ionic compound
will be soluble in water if the energy evolved in the hydration of the cation and
anion is greater than the lattice energy of the compound.
The sulphates of
group II elements decrease in solubility as the atomic number of the metal
increases (i.e. descending the group).
MgSO4 soluble
CaSO4 sparingly soluble
SrSO4 almost insoluble
BaSO4 almost insoluble
Explanation
The lattice
energies for the four are almost the same but
Ba2+ is
larger than Mg2+. The hydration energy of Mg2+ (being of
smaller ionic radius) will be larger than that of Ba2+. Therefore
MgSO4 is soluble, BaSO4 almost insoluble.
Analytical uses of the ions as exemplified by the use of barium ions to test for sulphate and sulphite, magnesium ions to distinguish between hydrogencarbonate and carbonate ions in solution; back titration to determine the purity of a group II metal, oxide or carbonate.
[See qualitative
analysis notes.]