Atomic Structure
Atomic Structure
e 1.062 10−19 C
= −1
= 1.67 10−24 g
e / m 958 10 Cg 4
As the mass of the electron is 9.1 x 10-28 g, the ratio of the mass of positive particle obtained from
hydrogen to the mass of an electron is,
1.67 10−24 g
= 1837
9.1 1028 g
The positive particle from hydrogen is 1837 times heavier than the electron. This positively charged
particle was called proton. The proton is produced by the loss of an electron from a neutral hydrogen
atom and is thus a hydrogen ion H+. The mass of H is found to be 1837 times that of an electron and so
the mass of the proton is nearly the same as that of a hydrogen atom.
10. If loss of radiation is continuous, than spectrum should be continuous but atomic spectrum is
always line spectrum
Q. 5 Write main postulates of Bohr’s atomic model.
(Bohr’s atomic model for hydrogen atom)
ANSWER. In 1913, Neils Bohr proposed a model of an atom based on the Planck's quantum theory
of radiation. The basic postulates of Bohr's theory are:
11. An atom consists of a small, heavily positively charged nucleus around which electrons revolve
in definite circular paths called orbits.
12. These orbits are associated with definite energies called energy shells/energy levels. They are
designated as K, L, M, N, …. etc. shells or numbered as 1, 2, 3, 4, …..etc. from the nucleus.
13. As long as the electron remains in a particular orbit /energy shell its energy remains constant.
This accounts for the stability of an atom.
14. Only those orbits are permitted in which angular momentum of the electron is a whole number
h
multiple of where h is Plancks constant. Any moving body taking a circular orbit has an
2
angular momentum equal to the product of its mass (m), velocity of movement (v) and radius of
orbit (r). In other words the angular momentum of an electron
h
mvr = n , where'n' = 1,2,3,
2
15. Electrons can either lose or absorb energy abruptly, when they jump from one energy level to
another. For instance when an electron moves from the 'normal or ground state - E1' of an atom
i.e., the state of lowest energy as required by its 'n' and 'l' values, to a higher level, it causes the
atom to be in its 'excited state - E2' i.e., where electrons in an atom occupy energy levels higher
than those permitted by its 'n' and 'l' values. The reverse is also true and the change in energy is
E, E = E2 − E1 = h
Q. 6 How the radius of hydrogen atom can be calculated by the help of Bohr’s atomic model.
(Examiner may ask What is radius of hydrogen atom?you can derive it from atomic model)
ANSWER. Hydrogen atom consist of one electron revolving aroung the nucleus( having one
proton)
v
e
r
Consider an electron of charge e revolving in an orbit of raius r. the centrifugal force acting on electron
mv 2
is F = ⎯⎯ → (1)
r
The electcastatic force(according to Coulomb’s laws ) of attraction between electron and nucleus is
given as
Ze e
F= or F = Ze2 /4o r2 → (2)
4o r 2
nh
v=
2mr
We see that distance between orbits goes on increasing when we move from Ist orbit to higher orbit.
It means that r2 − r1 r3 − r2 r4 − r3 − − − − −
Q. 7 Calculate the energy of electron on the bases of Bohr’s atomic model.
ANSWER. Total energy (E) of electron in an orbit is equal to the sum of its kinetic energy due to
motion and potential energy due to interaction with the nucleus. Thus; E = K.E + P.E -----1
1
Since, K.E = mv2 -----------2
2
Relation for potential energy is
1 qq
P.E = − 1 2
4 r
For nucleus (charge Ze) and electron (charge e) the relation is modified as
Ze.e
P.E = −
4 r
Ze2
P.E = − ⎯⎯
→ (3)
4 r
mv 2 Ze2
E= −
2 4o r
Ze2
Since, 2
v =
4 rm
m Ze2 Ze2 Ze2 1
E= − = −1
2 4 rm 4 r 4r 2
Ze2 1
E= −
4 r 2
Ze2
E= −
8o r
n2
Since, r = 5.39 x 10-11 (m)
Z
Ze2 Z
E=−
8 n2 5.39 10−11
e2 Z2
E = − −11 2
8 5.39 10 n
Where;
e2
−11
= constant = 2.18 10−18 J
8 5.39 10
Z2
E = – 2.18 10-18
n2
For hydrogen Z (atomic number) = 1
1
E = −2.18 10-18 2 J/atom
n
1
E = −1313 2 kJ / mol
n
The following sequence shows that how these calculations from J/atom to kJ/mol are carried out.
1
E = −2.18 10-18 2 J
n
1
E = −2.18 10-18 J /atom
n2
1
E = −2.18 10-18 10−3 kJ /atom
n2
1 1
E = −2.18 10-18 3
6.022 1023 2 kJ / mol
10 n
1
E = −13.13 10−18−3+23
n2
1
E = −13.13 102 KJ/mol
n2
For 1st orbital of hydrogen
E = - 1313 KJ/mol
Q. 8 Define atomic orbital, how you can distinguished between orbit and orbital?
ANSWER. According to wave mechanics, we cannot simply say that the electron exists at a
particular point but we talk about certain regions in space around the nucleus where the probability
of finding the electron is maximum. Such regions are expressed by mathematical expressions and are
called orbital wave functions or commonly known as orbitals. Therefore, the wave equation leads to
the concept of orbitals instead of well-defined circular orbits.
An orbital may be defined as the region in space around the nucleus where the probability of finding
the electron is maximum.
If a boundary is drawn which encloses a region where there is high probability (about 90 - 95%) of
finding the electron, the figure obtained gives the general picture of an orbital. However, it is difficult
to draw the real picture of an orbital. For the sake of simplicity, it may be represented as shown in the
figure given below.
ANSWER. Shapes of s orbitals: s orbitals are non-directional and spherically symmetrical, This
means that the probability of finding the electron is same in all directions at a particular distance from
the nucleus, The 1s orbital is shown in the figure
It is observed that density of charge cloud is maximum at the nucleus and decreases with increase in
distance from the nucleus. The 2s orbital is also non-directional and spherically symmetrical. In this
case, the density is maximum at the nucleus and becomes small at large distances. However, the
effective volume or size of 2s is larger than 1s orbital
Shapes of p orbitals: For p-orbitals (l=1), there are three possible orientations corresponding to m =
-1, 0, +1 values. This means that there are three p - orbitals in each p-subshell. These are designated as
px, py and pz; For e.g., 2px, 2py and 2pz.
These three orbitals are equal in energy but differ in their orientations. Each orbital consists of two
lobes symmetrical about a particular axis. Depending upon the orientation of the lobes, these are
designated as 2px, 2py and 2pz, as they are symmetrical about x, y and z-axes respectively.
Shapes of d orbitals: For d-orbital (l = 2), there are five possible orientations corresponding to m = -
2, -1, 0, + 1, +2. This means that there are five orbitals in each d-subshell. For 3d subshell, these are
designated as 3dxy, 3dyz, 3dxz, 3dx2- y2 and 3dz2. These five orbitals are equal in energy but differ in their
orientations. The shapes of 3d orbitals are shown in the figure.
Figure: s orbital
The p orbital (l = 1) has three orbitals, since m = -1, 0, and 1. These three orbitals lie along the x-, y-,
and z-axes.
Figure: p orbitals
The d orbital (l = 2) has five orbitals, since m = -2, -1, 0, 1, and 2. It is far more difficult to describe the
orientation of d orbitals, as you can see:
Figure: d orbitals
4. Spin Quantum Number (s)
The spin quantum number tells whether a given electron is spin up (+1/2) or spin down (-1/2). An
orbital contains two electrons, and each of those electrons must have different spins.
Note: no need to draw shapes of s, p or d in final examination if examiner ask just about quantum
number, these are for students guidance .
Q. 11 Write a detail note on electronic configuration.
(Examiner may ask only about Aufbua principle, Pauli’s Exclusion principle or Hund’s rule)
ANSWER. The distribution of electrons in different orbitals is known as its electronic
configuration. This characterizes each electron in an atom. The electronic configuration is expressed
by indicating the principal quantum number and its respective orbital along with the number of
electrons present in it. For example the notation 3px1 indicates that in the third principal shell there
is one electron in the 'px' orbital.
Sometimes the electronic configuration is also described by box notation form i.e., putting an arrow
for single electron in a box or a pair of arrows for two electrons in a box. The direction of the arrows
gives the orientation of its spin.
Further the box is labeled on top by writing the symbol of the orbital.
6. Pauli's exclusion principle: The Paulis exclusion principle states, that no two electrons in an
atom can have the same values of all the four quantum numbers. If one electron in the atom has
the quantum numbers n = 1, l = 0, m = 0 and s = +1/2, no other electron can have the same four
quantum numbers. In other words, we cannot place two electrons with the same value of 's' in a
'1s' orbital.
Secondly, each orbital can accommodate a maximum of two electrons only if their spins are of
opposite directions. Each sub shell holds a maximum of two electrons in an orbital.
Note: It can be inferred that the maximum number of orbital in each shell is n 2 and the maximum
number of electrons is 2n2.
7. Hund's rule of maximum multiplicity: It states that when more than one orbital of equal
energies are available then the electrons will first occupy these orbitals separately with parallel
spins. The pairing of electrons will start only after all the orbitals of a given sub level are singly
occupied. This is because electrons with parallel spins tend to be as far apart as possible to
minimize the electrostatic repulsion.
For example, the three electrons that are filled into the three 'p' orbitals can be represented in two
different ways:
24. Determine the electronic configuration of an atom X having four set of quantum numbers
for the valence electron as follow; n=4, l=1, m=1, ms=+1/2
a. x:1s2,2s2,2p6,3s2,3p6,4s2,4p1. b. x:1s2,2s2,2p6,3s2,3p6,4s2
c. x:1s ,2s ,2p ,3s ,3p
2 2 6 2 1 d. x:1s2,2s2,2p6,3s2,3p6
Ans. a (x:1s2,2s2,2p6,3s2,3p6,4s2,4p1)