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Structure & Bonding of the Period 3 Elements (CIE A Level Chemistry)

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Explaining Physical Properties of the Period 3 Elements

Melting point

Melting points of the elements across Period 3 table

Period 3 element Na Mg Al Si P S Cl Ar
Melting point
(K)
371 923 932 1638 317 392 172 84

Graph of melting points across Period 3

The Periodic Table - Melting Point Graph, downloadable AS & A Level Chemistry revision notes

There is a general increase in melting point from Na to Si, followed by a sharp drop to the lower melting points of P to Ar

  • The above trends can be explained by looking at the bonding and structure of the elements

Bonding and structure of the Period 3 elements table

Period 3 element Na Mg Al Si P S Cl Ar
Bonding Metallic Metallic Metallic Covalent Covalent Covalent Covalent -
Structure Giant metallic Giant metallic Giant metallic Giant molecular Simple molecular Simple molecular Simple molecular Simple molecular

  • 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 structure of metals

The Periodic Table - Metallic Lattice, downloadable AS & A Level Chemistry revision notes

Metal cations form a giant lattice held together by electrons that can freely move around

  • 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 electrons
  • 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 is much larger compared to a 1+ ion and the smaller number of delocalised electrons in Na
  • Due to this, the melting points increase going from Na to Al
  • 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 a single atom)
  • 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

  • The electrical conductivity decreases going across the Period 3 elements

Trends in electrical conductivity across Period 3 table

Period 3 element Na Mg Al Si P S Cl Ar
Electrical conductivity
(S m-1)
0.218 0.224 0.382 2 x 10-10 10-17 10-23 - -

 

  • 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, in Al there are more electrons available 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

Examiner Tip

  • Intermolecular forces are forces between molecules
  • Intramolecular forces are forces within a molecule

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Caroline

Author: Caroline

Expertise: Physics Lead

Caroline graduated from the University of Nottingham with a degree in Chemistry and Molecular Physics. She spent several years working as an Industrial Chemist in the automotive industry before retraining to teach. Caroline has over 12 years of experience teaching GCSE and A-level chemistry and physics. She is passionate about creating high-quality resources to help students achieve their full potential.