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Quantum Physics and Electronic Configurations in Chemical Physics, Slides of Nutrition

An overview of quantum physics principles, such as hund's rule and the pauli exclusion principle, and their application in determining electronic configurations of elements in the periodic table. It includes examples of ground-state configurations and a class exercise for determining the electronic configurations of potassium and calcium.

Typology: Slides

2011/2012

Uploaded on 12/23/2012

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Hund’s rule: The lowest energy state of an atom is achieved when there is maximum
utilization of the surrounding space by the occupying electrons. Pairing of electrons in an
orbital is recognized as a higher energy state than single electrons of the same spin state
occupying the orbitals. This does not apply to s orbitals.
Pauli exclusion principle: No two electrons in an atomic orbital may share the same
set of quantum numbers. This rule led to the realization that electrons in the same
orbital must be of opposite spins.
Two Major Rules in Chemical Physics that impinge on the behavior of minerals
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Hund’s rule: The lowest energy state of an atom is achieved when there is maximum utilization of the surrounding space by the occupying electrons. Pairing of electrons in an orbital is recognized as a higher energy state than single electrons of the same spin state occupying the orbitals. This does not apply to s orbitals.

Pauli exclusion principle: No two electrons in an atomic orbital may share the same set of quantum numbers. This rule led to the realization that electrons in the same orbital must be of opposite spins.

Two Major Rules in Chemical Physics that impinge on the behavior of minerals

2s

X

Y

Z

1s

2px

2px 2py 2py

2pz

2pz

3s

1s 2s, 2p

n= n= n=3 3s, 3p, 3d

2s

(K shell) (L shell) (M shell)

Quant No. (^) Configuration.

2 p orbitals. At the second quantum level orientation also becomes a factor in deciding orbital energy. Because there are 3 orientations existing simultaneously, a p orbital can hold a maximum of 6 electrons, 2 of opposite spin in each

Shapes are the same, but differ in orientation

Element (At. No.)

Ground-state configuration

Abbreviated form

Sodium (11) 1 s^22 s^22 p^63 s^1 [Ne]3 s^1

Magnesium (12) 1 s^22 s^22 p^63 s^2 [Ne]3 s^2

Aluminum (13) 1 s^22 s^22 p^63 s^23 p^1 [Ne]3 s^23 p^1

Silicon (14) 1 s^22 s^22 p^63 s^23 p^2 [Ne]3 s^23 p^2

Phosphorus (15) 1 s^22 s^22 p^63 s^23 p^3 [Ne]3 s^23 p^3

Sulfur (16) 1 s^22 s^22 p^63 s^23 p^4 [Ne]3 s^23 p^4

Chlorine (17) 1 s^22 s^22 p^63 s^23 p^5 [Ne]3 s^23 p^5

Argon (18) 1 s^22 s^22 p^63 s^23 p^6 [Ne]3 s^23 p^6

Caution:

The 4 s orbital is actually at a lower energy level than the 3 d. As a result 4 s orbitals will fill before 3 d. But, when ionized, electrons will be lost from the 4 s before the 3 d

K = 1 s 2 s 2 p 3 s 3 p 3 d 4 s

Ca = 1 s^2 2 s^2 2 p^6 3 s^2 3 p^6 3 d 4 s^2

Solution: When n = 3, the atom must contain s, p, and d subshells and 3 energy states. But, recall that the 4s subshell with 2 electrons is of a lower energy state than the 3d subshell and will fill first

The most stable form occurs when both metals lose their 4s electrons. Thus:

K+^ and Ca2+

[Ar]4 s^1 and [Ar]4 s^2

Z = 19

Z = 20

First transition series

Macrominerals

Microminerals

3 d

4 d

5 d

1. Why do Ca2+^ , Mg 2+^ , and Zn2+^ exist only as +2 ions? Li+^ , Na +^ and K+^ as +1 ions?

  • Ca = [Ar] 4s
  • Mg = [Ne] 3s
  • Zn = [Ar] 3d 10 4s - Li = [He] 2s
  • Na = [Ne] 3s
    • K = [Ar]4s

Fe element No. 26

1 s^2 2 s^2 2 p^6 3 s^2 3 p^6 4 s^2 3 d^6

Z Z

Z Z

Z

X

X

X

X

Y^ Y^ X Y

Y Y

dxy

d yz

dxz

d X 2 -Y 2 dZ^2