Atomic Structure
Atomic Structure
What happens if a beam of each of these particles is passed between two electrically charged plates - one positive and
one negative
Protons are positively charged and so would be deflected on a curving path towards the negative plate.
Electrons are negatively
charged and so would be
deflected on a curving path
towards the positive plate.
Neutrons don't have a charge,
and so would continue on in a
straight line.
Nucleon No is the sum of protons and neutrons present in a nucleus. Complete the following table.
ISOTOPES:-
ISOTOPES:- are the atoms, which have the same atomic number but different mass numbers.
OR.
Isotopes are atoms with same no of protons but different no of neutrons.
e.g. Hydrogen has 3 isotopes. Their Structures are shown :
35
Chlorine-35 and Chlorine -37 are examples of isotopes. 17𝐶𝐶𝐶𝐶 and 37
17𝐶𝐶𝐶𝐶
Average mass of isotopes can be calculated if we known their relative abundance. Cl – 35 is 75% and Cl – 37 is 25%.
35 × 75 + 37 × 25
=
100
= 35.5
NOTE Relative abundance of Isotopes is calculated by using Mass Spectrometer. The Mass Spectrum can be given as
35 × 3 + 37 × 1
=
4
= 35.5
Electronic Configuration
The principal quantum shells ( Orbits) can be divided into subshells. The levels (or shells) are numbered as 1 , 2 , 3, 4, 5,
etc. and the subshells ( Orbitals) are indicated by the letters s, p, d, or f. The maximum no of electrons that can be
present in a sub – shell are given in table
Sub Shells Max Electrons
First principal quantum shell can have maximum 2 s 2
electrons. These 2 electrons are present in s orbitals. p 6
d 10
2nd shell can have maximum 8 electrons. 2 are present in f 14
s subshell and 6 are present in p subshell. Similarly in
3rd shell, maximum 18 electrons can be present. 2 in s subshell, 6 in p subshell and 10 in d subshell can be present.
Principal Quantum Shell No of Electrons(2n2) Orbital
1 2 s
2 8 s, p
3 18 spd
4 32 spdf
Subshell Atomic orbitals Total Electrons NOTE:- s has only one orbital
s s 1*2=2 p orbitals are named as px, py and pz. These orbitals are
p p p p 3*2=6 degenerate. d orbitals are named as dxy dyz dxz
d d d d d d 5 * 2 = 10 dx2 – y2 dz2. These orbitals are also degenerate
f f f f f f f f 7 * 2 = 14
Shapes of s and p orbitals
Energy level of orbitals
Filling Orbitals
Three important rules for filling electrons in orbitals are as
I. Aufbau Rule. Lowest energy orbitals are filled first. Thus, the filling pattern
is 1s, 2s, 2p ,3s,3p,4s , 3d, etc.
II. Hund’s Rule. Electrons prefer to live as unpaired electron in orbitals as long
as possible, all possessing the same spin direction.
III. Pauli Exclusion Principle. Only two electrons are permitted per orbital and
they must be of opposite spin.
Orbitals can be represented as boxes. Each box shows one orbital. Electrons are represented as arrows, direction of
arrows show spin of electrons. When two electrons are present in orbital, then there arrows are in opposite direction.
2500
first ionisation energy (kJ
2000
per mole)
1500
1000
500
0
0 5 10 15 20
atomic number
First ionization energy is different for different elements as shown in graph. This graph shows a periodicity. From Li to
Ne, it is increasing, then again increasing from Na to Ar.
various trends in this graph which can be explained by reference to the proton number and electronic configuration of
the various elements. A number of factors must be considered
In general, the first ionisation energy increases across a period because the nuclear charge increases but the shielding
remains the same.
From B (1s22s22p1) to N (1s22s22p3) the proton number increases, but the number of electrons shielding the nuclear
charge remains the same. Thus the effective nuclear charge increases from B to N and the electrons become
progressively harder to remove and Thus the first ionisation energy increases from B to N.
The electronic configurations of N and O must be considered more carefully:
1s 2s 2p
N ↑↓ ↑↓ ↑ ↑ ↑
O ↑↓ ↑↓ ↑↓ ↑ ↑
Note that in N the electron is removed from an unpaired orbital, but in O it is removed from a paired orbital. In a paired
orbital, the two electrons share a confined space and so repel each other. They are therefore less stable and easier to
remove. This repulsion effect reduces the higher effective nuclear charge in O.
Thus the first ionisation energy of O is lower than that of N. The first ionisation energies increase as expected from O to
Ne, due to the increase in effective nuclear charge.
So in period 2 the first ionisation energy increases across a period but two exceptions are seen,
The same trend can also be found in Period 3 (Na - Ar). There is a general increase,
but a drop between Mg and Al and also between P and S.
As you go down a group in the Periodic Table ionisation energies generally fall.
This is because the electron to be removed from the outer energy level is
increasingly distant from the nucleus, as a result the attraction of the nucleus for the
electron becomes less, and it becomes easier to pull electron away.
Electrons in the inner energy levels also produce a screening effect. These inner electrons reduce the attraction of the
nucleus for the outer electrons. The screening effect will increase as the number of inner energy levels increases.
The amount of energy needed for removing all the electrons (one by one) of a gaseous atom is known as successive
ionization energies. These are basically termed as 1st , 2nd, 3rd or 4th …… ionization energy and these depends
completely on the removal of the 1st, 2nd, 3rd electrons respectively.
1st ionization energy
• 2nd ioniza�on Energy: It is the energy needed to remove a second X →(g)X+ + (g)
e−
electron from each ion in 1 mole of gaseous 1+ ions to give gaseous
2nd ionization energy
2+ ions.
• 3rd ioniza�on Energy: It is the energy needed to remove a third X+ →(g)X2+ +(g)e−
electron from each ion in 1 mole of gaseous 2+ ions to give gaseous 3rd ionization energy
3+ ions.
X2+ → X(g)3+ + e(g)−
Once you have removed the first electron you are left with a positive ion. Trying to remove a negative electron from a
positive ion is going to be more difficult than removing it from an atom. Removing an electron from a 2+ or 3+ (etc) ion is
going to be progressively more difficult. So the value of successive ionization energies increase. This increase in values
are very helpful in finding the electronic structure of atoms.
This shows that there are three electrons, 1 in the outermost sub – shell and two in inner sub – shell. So the inner sub
shell is 1s and Outer sub shell is 2s. The electronic configuration will be as 1s2, 2s1.
This configuration also shows that there are two principal quantum shell as there is a big jump (multiples of 519) in values
from 519 to 7300.
ionisation energy
These IE are closer to each other as 3 electrons are 100000
removed from third shell (i.e. 3s23p1) but there is a huge 10000
4th: 11578 kJmol-1, 5th: 14831 kJmol-1, 6th: 18378 kJmol-1 7th: 23296 kJmol-1, 8th: 27460 kJmol-1, 9th: 31862 kJmol-
1
10th: 38458kJmol-1, 11th: 42655 kJmol-1. From 4th to 11th , there is a smooth increase in IE, so these 8 electrons are
removed from same shell. There is a huge jump to the12th ionisa�on energy, and this show that electron removed
from further inner shell. This 12th electron is removed from 1s and 13th is also removed from 1s.