Atomic Structure :  Periodic Trends

Atomic Radii

1) As you move down a group, atomic radius increases.

  • WHY? - The number of energy levels increases as you move down a group as the number of electrons increases.  Each subsequent energy level is further from the nucleus than the last.  Therefore, the atomic radius increases as the group and energy levels increase.
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2) As you move across a period, atomic radius decreases.

View a periodic table with atomic radii.

Ionic Radii

1) Anions (negative ions) are larger than their respective atoms.

2) Cations (positive ions) are smaller than their respective atoms.

First Ionization Energy

1) As you move down a group, first ionization energy decreases.

2) As you move across a period, first ionization energy increases.

Exceptions to First Ionization Energy Trends

1) Xs2 > Xp1  e.g.  4Be > 5B
  • WHY? - The energy of an electron in an Xp orbital is greater than the energy of an electron in its respective Xs orbital.  Therefore, it requires less energy to remove the first electron in a p orbital than it is to remove one from a filled s orbital.

2) Xp3 > Xp4  e.g.  7N > 8O

  • WHY? - After the separate degenerate orbitals have been filled with single electrons, the fourth electron must be paired.  The electron-electron repulsion makes it easier to remove the outermost, paired electron.
    (See
    Hund's Rule)      

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Veiw a periodic table with first ionization energies.

Second and Higher Ionization Energies

Ionization Energies (kJ/mol)

Element
Na
Mg
Al

   

1st IE
495.8
737.7
577.6

   

2nd IE
4562.4
1450.6
1816.6

   

3rd IE
6912
7732.6
2744.7

   

4th IE
9543
10,540
11,577

Electron Affinity

1) As you move down a group, electron affinity decreases.

2) As you move across a period, electron affinity increases.

Exceptions
  • Among nonmetals, however, the elements in the first period have lower electron affinities than the elements below them in their respective groups.
  • Elements with electron configurations of Xs2, Xp3, and Xp6 have electron affinities less than zero because they are unusually stable.  In other words instead of energy being given off, these elements actually require an input of energy in order to gain electrons.  e.g.  Be, N, Ne
    • WHY? - Electron affinities are all much smaller than ionization energies.
      1. Xs2 < 0:  Stable, diamagnetic atom with no unpaired electrons.
      2. Xp3 < 0: Stable atom with 3 unpaired p-orbital electrons each occupying its own subshell.
      3. Xp6 < 0: Stable atom with filled valence (outermost) shell.

Lattice Energy

The strength of a bond between ions of opposite charge can be calculated using Coulomb's Law.

Coulomb's Law - The force of attraction between oppositely charged particles is directly proportional to the product of the charges of the particles (q1 and q2) and inversely proportional to the square of the distance between the particles.

1) As you move down a group, lattice energy decreases.

2) As you increase the magnitude of the charge (becomes more positive or more negative), lattice energy increases.

Lattice Energies of Alkali Metals
with Halides (kJ/mol)
Li+
Na+
K+
Rb+
Cs+
F-
1036
923
821
785
740
Cl-
853
787
715
689
659
Br-
807
747
682
660
631
I-
757
704
649
630
604

           

Lattice Energies of Salts
of OH- and O2- with Cations
of varying charge (kJ/mol)

Na+
Mg2+
Al3+

OH-
900
3006
5627

O2-
2481
3791
15916

Next:  "Metals, Nonmetal, and Semimetals"