9.1 Periodicity of Physical Properties of The Elements in Period 3
9.1 Periodicity of Physical Properties of The Elements in Period 3
9.1 Periodicity of Physical Properties of The Elements in Period 3
Atomic radius
The atomic radius is the distance between the nucleus and the outermost electron of
an atom
The atomic radius is measured by taking two atoms of the same element, measuring the
distance between their nuclei and then halving this distance
In metals this is also called the metallic radius and in non-metals, the covalent radius
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Ionic radius
Going across the period from Na+ to Si4+ the ions get smaller due to
the increased nuclear charge but same shielding effect. So the attraction between the
outer electrons and the nucleus increases.
The anions are bigger than their original atoms because each atom has gained one or
more electrons in the same shell. This increases the repulsion between electrons while
the nuclear charge is still the same
Going across P3- to Cl– the ionic radii decreases as the nuclear charge increases but
shielding remain same. So increase attraction between outermost electron and the
nucleus.
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Ionic radii of ions of Period 3 elements table
Melting point
The above trends can be explained by looking at the bonding and structure of the
elements which are summarised in the table below
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Bonding & structure of Period 3 elements table
The table shows that Na, Mg and Al are metallic elements which form positive ions
arranged in a giant lattice in which the ions are held together by a ‘sea’ of delocalised
electrons around them:
The electrons in the ‘sea’ of delocalised electrons are those from the valence shell of
the atoms
Na will donate one electron into the ‘sea’ of delocalised electrons, Mg will donate two
and Al three
As a result of this, the metallic bonding in Al is stronger than in Na
This is because the electrostatic forces between a 3+ ion and the larger number of
negatively charged delocalised electrons are much larger compared to a 1+ ion and the
smaller number of delocalised electrons in Na
Because of this, the melting points increase going from Na to Al
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Si has the highest melting point due to its giant molecular structure in which each Si
atom is held to its neighbouring Si atoms by strong covalent bonds
P, S, Cl and Ar are non-metallic elements and exist as simple molecules (P4, S8,
Cl2 and Ar as single atoms)
The covalent bonds within the molecules are strong, however between the molecules
there are only weak instantaneous dipole-induced dipole forces
It doesn’t take much energy to break these intermolecular forces
Therefore, the melting points decrease going from P to Ar (note that the melting point of
S is higher than that of P as sulphur exists as larger S8 molecules compared to the
smaller P4 molecule)
Electrical conductivity
As mentioned before, going from Na to Al, there is an increase in the number of valence
electrons that are donated to the ‘sea’ of delocalised electrons
Because of this, there are more electrons available in Al to move around through the
structure when it conducts electricity, making Al a better electrical conductor than Na
Due to the giant molecular structure of Si, there are no delocalised electrons that can
freely move around within the structure
Si is therefore not a good electrical conductor and is classified as
a semimetal (metalloid)
The lack of delocalised electrons is also why P and S cannot conduct electricity
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