Iit - JEE Syllabus: RSM79 PH I AS CH 1

RSM79PhIASCH1
1. IIT–JEE Syllabus
Atomic structure; Rutherford Model; Spectrum of hydrogen atom; Bohr model;
de Broglie relations, Uncertainty principle, Quantum model; Electronic configuration
of elements ( upto to atomic number 36); Aufbau principle, Pauli’s exclusion principle
and Hund’s rule, shapes of s,p, and d orbitals.
2. Dalton’s Atomic Theory

All the objects around you, this book, your pen or pencil and things of nature such as rocks,
water and plant constitute the matter of the universe. Matter is any substance which
occupies space and has mass.
Dalton, in 1808, proposed that matter was made up of extremely small, indivisible particles
called atoms. (In Greek atom means which cannot be cut). This concept was accepted for
number of years.
The main postulates of Dalton’s atomic theory are

 Matter is made up of small indivisible particles, called atoms.
 Atoms can neither be created nor destroyed. This means that a chemical reaction is
just a simple rearrangement of atoms and the same number of atoms must be present
before and after the reaction.
 Atom is the smallest particle of an element which takes part in a chemical reaction.
 Atoms of the same element are identical in all respects especially, size, shape and
mass.
 Atoms of different elements have different mass, shape and size.
 Atoms of different elements combine in a fixed ratio of small whole numbers to form
compound atoms, called molecules.
However, the researches done by various eminent scientists and the discovery of
radioactivity have established beyond doubt, that atom is not the smallest indivisible particle
but had a complex structure of its own and was made up of still smaller particles like
electrons, protons, neutrons etc. At present about 35 different subatomic particles are
known but the three particles namely electron, proton and neutron are regarded as the
fundamental particles.
We shall now take up the brief study of these fundamental particles. The existence of
electrons in atoms was first suggested, by J.J. Thomson, as a result of experimental work on
the conduction of electricity through gases at low pressures and high voltage, which
produces cathode rays consisting of negatively charged particles, named as electrons. The
e/m ratio for cathode rays is fixed whose values is 1.76  108 C/g
We know that an atom is electrically neutral, if it contains negatively charged electrons it

must also contain some positively charged particles. This was confirmed by Goldstein in his
discharge tube experiment with perforated cathode. On passing high voltage between the
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electrodes of a discharge tube it was found that some rays were coming from the side of the
anode which passed through the holes in the cathode. These anode rays (canal rays)
consisted of positively charged particles formed by ionization of gas molecules by the
cathode rays. The charge to mass ratio ( e/m value) of positively charge particles was found
to be maximum when the discharge tube was filled with hydrogen gas as hydrogen is the
lightest element. These positively charged particles are called protons.
e/m varies with the nature of gas taken in the discharge tube. The positive particles are
positive residues of the gas left when the gas is ionized.
The neutral charge particle, neutron was discovered by James Chadwick by bombarding
boron or beryllium with –particles.
Characteristics of the three fundamental particles are:

Electron Proton Neutron
Symbol e or e– p n
Approximate relative mass 1/1836 1 1
Approximate relative charge –1 +1 No charge
Mass in kg 9.10910–31 1.67310–27 1.67510–27
Mass in amu 5.48510–4 1.007 1.008
Actual charge (coulomb) 1.60210–19 1.60210–19 0
Actual charge (e.s.u.) 4.8  10–10 4.8  10–10 0
The atomic mass unit (amu) is 1/12 of the mass of an individual atom of 6C12, i.e.,
1.66010–27 kg.
The neutron and proton have approximately equal masses of 1 amu and the electron is
about 1836 times lighter, its mass can sometimes be neglected as an approximation.
The electron and proton have equal, but opposite, electric charges while the neutron is not
charged.
3. Atomic Models
We know the fundamental particles of the atom. Now let us see, how these particles are
arranged in an atom to suggest a model of the atom.
3.1 Thomson’s Model
J.J. Thomson, in 1904, proposed that there was an equal and opposite positive charge
enveloping the electrons in a matrix. This model is called the plum – pudding model after a
type of Victorian dissert in which bits of plums were surrounded by matrix of pudding.
electron
Positive sphere
This model could not satisfactorily explain the results of scattering experiment carried out by
Rutherford who worked with Thomson.
3.2 Rutherford’s Model
– particles emitted by radioactive substance were shown to be dipositive Helium ions

(He++) having a mass of 4 units and 2 units of positive charge.
Rutherford allowed a narrow beam of –particles to fall on a very thin gold foil of thickness
of the order of 0.0004 cm and determined the subsequent path of these particles with the
help of a zinc sulphide fluorescent screen. The zinc sulphide screen gives off a visible flash
of light when struck by an  particle, as ZnS has the remarkable property of converting
kinetic energy of  particle into visible light. [For this experiment, Rutherford specifically
used  particles because they are relatively heavy resulting in high momentum].
Observation
i) Majority of the –particles pass straight through the gold strip with little or no deflection.
ii) Some –particles are deflected from their path and diverge.
iii) Very few –particles are deflected backwards through angles greater than 90.
iv) Some were even scattered in the opposite direction at an angle of 180 [ Rutherford was
very much surprised by it and remarked that “It was as incredible as if you fired a 15–
inch shell at a piece of tissue paper and it came back and hit you”]. There is far less
difference between air and bullet than there is between gold atoms and -particles
assuming of course that density of a gold atom is evenly distributed.
Conclusions
1. The fact that most of the  - particles passed straight through the metal foil indicates the
most part of the atom is empty.
2. The fact that few  - particles are deflected at large angles indicates the presence of a
heavy positively charge body i.e., for such large deflections to occur  - particles must
have come closer to or collided with a massive positively charged body.
3. The fact that one in 20,000 have deflected at 180° backwards indicates that volume
occupied by this heavy positively charged body is very small in comparison to total
volume of the atom.
Atomic model
On the basis of the above observation, and having realized that the rebounding -particles
had met something even more massive than themselves inside the gold atom, Rutherford
proposed an atomic model as follows.
i) All the protons (+ve charge) and the neutrons (neutral charge) i.e nearly the total mass
of an atom is present in a very small region at the centre of the atom. The atom’s central
core is called nucleus.
ii) The size of the nucleus is very small in comparison to the size of the atom. Diameter of
the nucleus is about 10–13cm while the atom has a diameter of the order of 10–8 cm. So,
the size of atom is 105 times more than that of nucleus.
ii) Most of the space outside the nucleus is empty.
iv) The electrons, equal in number to the net nuclear positive charge, revolve around the
nucleus with fast speed in various circular orbits.
v) The centrifugal force arising due to the fast speed of an electron balances the
coulombic force of attraction of the nucleus and the electron remains stable in its path.
Thus according to him atom consists of two parts (a) nucleus and (b) extra nuclear part.
Defects of Rutherford’s atomic model
1. Position of electrons: The exact positions of the electrons from the nucleus are not
mentioned
2. Stability of the atom: Neils Bohr pointed out that Rutherford’s

atom should be highly unstable. According to the law of
electro–dynamics, the electron should therefore, continuously
emit radiation and lose energy. As a result of this a moving
+
electron will come closer and closer to the nucleus and after
passing through a spiral path, it should ultimately fall into the
nucleus.
It was calculated that the electron should fall into the nucleus in less than 10–8 sec. But it is
known that electrons keep moving outside the nucleus.
To solve this problem Neils Bohr proposed an improved form of Rutherford’s atomic model.
Before going into the details of Neils Bohr model we would like to introduce you some
important atomic terms.
Atomic terms
a) Atomic Number (Z): The atomic number of an element is the number of protons
contained in the nucleus of the atom of that element.
b) Nucleons: Protons and neutrons are present in a nucleus. So, these fundamental
particles are collectively known as nucleons.
c) Mass Number (A): The total number of protons and neutrons i.e, the number of
nucleons present in the nucleus is called the mass number of the element.
d) Nuclide: Various species of atoms in general. A nuclide has specific value of atomic
number and mass number.
IUPAC notation of an atom (nuclide)
Let X be the symbol of the element. Its atomic number be Z and mass number be A.
Then the element can be represented as Z X A
e) Isotopes: Atoms of the element with same atomic number but different mass number
e.g. 1H1, 1H2, 1H3. There are three isotopes of hydrogen.
32
f) Isobars: Atoms having the same mass number but different atomic numbers, e.g. 15P
and 16S32 are called isobars.
g) Isotones: Atoms having the same number of neutrons but different number of protons or
mass number, e.g. 6C14, 8O16, 7N15 are called isotones.
h) Isoelectronic: Atoms, molecules or ions having same number of electrons are
isoelectronic e.g. N2,CO, CN–.
i) Nuclear isomer: Nuclear isomers (isomeric nuclei) are the atoms with the same atomic
number and same mass number but with different radioactive properties.
Example of nuclear isomers is
Uranium –X (half life 1.4 min) and
Uranium –Z (half life 6.7 hours)
The reason for nuclear isomerism is the different energy states of the two isomeric
nuclei.
Other examples are
69 69
30Zn 30Zn
(T1/2 = 13.8 hr) (T1/2 = 57 min)
80 80
35Br 35Br
(T1/2 = 4.4 hour) (T1/2 = 18 min)
j) Isosters: Molecules having same number of atoms and also same number of electrons
are called isosters.
E.g., (i) N2 and CO
ii) CO2 and N2O
iii) HCl and F2
k) Atomic mass unit: Exactly equal to 1/12 of the mass of 6C12 atom
1 amu = 1.66 10–27 kg = 931.5 MeV
4. Some Important Characteristics of a Wave

A wave is a sort of disturbance which originates from some vibrating source and travels
outward as a continuous sequence of alternating crests and troughs. Every wave has five
important characteristics, namely, wavelength (), frequency (), velocity (c), wave number
  and amplitude (a).
Crest  Crest

Trough Trough
Ordinary light rays, X–rays,–rays, etc. are called electromagnetic radiations because similar
waves can be produced by moving a charged body in a magnetic field or a magnet in an
electric field. These radiations have wave characteristics and do not require any medium for
their propagation.
i) Wave length (): The distance between two neighbouring troughs or crests is known as
wavelength. It is denoted by  and is expressed in cm, m, nanometers (1nm=10–9m) or
Angstrom (1Å=10–10m).
ii) Frequency (): The frequency of a wave is the number of times a wave passes through
a given point in a medium in one second. It is denoted by (nu) and is expressed in
cycles per second (cps) or hertz (Hz) 1Hz = 1cps.
The frequency of a wave is inversely proportional to its wave length ()
1 c
 or  =
 
iii) Velocity: The distance travelled by the wave in one second is called its velocity. It is
denoted by c and is expressed in cm sec–1.
c
c =  or  =

iv) Wave number   : It is defined as number of wavelengths per cm. It is denoted by

 and is expressed in cm–1.
1 
 = (or)  =
 c
v) Amplitude: It is the height of the crest or depth of the trough of a wave and is denoted
by a. It determines the intensity or brightness of the beam of light.
Wavelengths of electromagnetic radiations

Electromagnetic radiations Wave length (Å)
Radio waves 31014 to 3 107
Micro waves 3109 to 3 106
Infrared (IR) 6106 to 7600
Visible 7600 to 3800
Ultra violet (UV) 3800 to 150
X–rays 150 to 0.1
Gamma rays 0.1 to 0.01
Cosmic rays 0.01 to zero
5. Atomic Spectrum
If the atom gains energy the electron passes from a lower energy level to a higher energy
level, energy is absorbed that means a specific wave length is absorbed. Consequently, a
dark line will appear in the spectrum. This dark line constitutes the absorption spectrum.
If the atom loses energy, the electron passes from higher to a lower energy level, energy is
released and a spectral line of specific wavelength is emitted. This line constitutes the
emission spectrum.
Hydrogen Atom
If an electric discharge is passed through hydrogen gas taken in a discharge tube under low
pressure, and the emitted radiation is analysed with the help of spectrograph, it is found to
consist of a series of sharp lines in the UV, visible and IR regions. This series of lines is
known as line or atomic spectrum of hydrogen. The lines in the visible region can be directly
seen on the photographic film.
Each line of the spectrum corresponds to a light of definite wavelength. The entire spectrum
consists of six series of lines each series, known after their discoverer as the Balmer,
Paschen, Lyman, Brackett, Pfund and Humphrey series. The wavelength of all these series
can be expressed by a single formula.
1  1 1
  = R   2 
 2
 n1 n2 
Where,
 = wave number
 = wave length
R = Rydberg constant (109678 cm–1)
n1 and n2 have integral values as follows
Series n1 n2 Main spectral lines
Lyman 1 2,3,4, etc Ultra – violet
Balmer 2 3,4,5 etc Visible
Paschen 3 4,5,6 etc Infra – red
Brackett 4 5,6,7 etc Infra – red
Pfund 5 6,7,8, etc Infra – red
[Note: All lines in the visible region are of Balmer series but reverse is not true. i.e., all
Balmer lines will not fall in visible region]
The pattern of lines in atomic spectrum is characteristic of hydrogen.
Types of Emission spectra
i) Continuous spectra: When white light from any source such as sun or bulb is
analysed by passing through a prism, it splits up into seven different wide bands of
colour from violet to red (like rainbow). These colour are so continuous that each of
them merges into the next. Hence the spectrum is called as continuous spectrum.
ii) Line spectra: When an electric discharge is passed through a gas at low pressure light
is emitted. If this light is resolved by a spectroscope, It is found that some isolated
coloured lines are obtained on a photographic plate separated from each other by dark
spaces. This spectrum is called line spectrum. Each line in the spectrum corresponds to
a particular wavelength. Each element gives its own characteristic spectrum.
6. Planck’s quantum theory

When a black body is heated, it emits thermal radiations of different wavelengths or
frequency. To explain these radiations, Max Planck put forward a theory known as Planck’s
quantum theory. The main points of quantum theory are
i) Substances radiate or absorb energy discontinuously in the form of small packets or

bundles of energy.
ii) The smallest packet of energy is called quantum. In case of light the quantum is known
as photon.
iii) The energy of a quantum is directly proportional to the frequency of the radiation . E  
(or) E = h were  is the frequency of radiation and h is Planck’s constant having the
value 6.626  10–27 erg – sec or 6.626  10–34 J–sec.
iv) A body can radiate or absorb energy in whole number multiples of a

quantum h, 2h,3h………..nh. where n is the positive integer.
Neils Bohr used this theory to explain the structure of atom.
7. Bohr’s Atomic Model

Bohr developed a model for hydrogen atom and hydrogen like one–electron species
(hydrogenic species). He applied quantum theory in considering the energy of an electron
bound to the nucleus.
Important postulates
 An atom consists of a dense nucleus situated at the centre with the electron revolving
around it in circular orbits without emitting any energy. The force of attraction between
the nucleus and an electron is equal to the centrifugal force of the moving electron.
 Of the finite number of circular orbits around the nucleus, an electron can revolve only in
those orbits whose angular momentum (mvr) is an integral multiple of factor h 2
nh
mvr =
2
where, m = mass of the electron
v = velocity of the electron
n = orbit number in which electron is present
r = radius of the orbit
 As long as an electron is revolving in an orbit it neither loses nor gains energy. Hence
these orbits are called stationary states. Each stationary state is associated with a
definite amount of energy and it is also known as energy levels. The greater the
distance of the energy level from the nucleus, the more is the energy associated with it.
The different energy levels are numbered as 1,2,3,4, ( from nucleus onwards) or
K,L,M,N etc.
 Ordinarily an electron continues to move in a particular stationary state without losing

energy. Such a stable state of the atom is called as ground state or normal state.
 If energy is supplied to an electron, it may jump (excite) instantaneously from lower

energy (say 1) to higher energy level (say 2,3,4, etc.) by absorbing one or more quanta
of energy. This new state of electron is called as excited state. The quantum of energy
absorbed is equal to the difference in energies of the two concerned levels.
Since the excited state is less stable, atom will lose it’s energy and come back to the
ground state.
Energy absorbed or released in an electron jump, (E) is given by
E = E2 – E1 = h
where E2 and E1 are the energies of the electron in the first and second energy levels,
and  is the frequency of radiation absorbed or emitted.
[Note: If the energy supplied to hydrogen atom is less than 13.6 eV, it will accept or
absorb only those quanta which can take it to a certain higher energy level i.e.,
all those photons having energy less than or more than a particular energy level
will not be absorbed by hydrogen atom. But if energy supplied to hydrogen atom
is more than 13.6 eV then all photons are absorbed and excess energy appear
as kinetic energy of emitted photo electron].
Radius and Energy levels of hydrogen atom
Consider an electron of mass ‘m’ and charge ‘e’ revolving around a nucleus of charge Ze
(where, Z = atomic number and e is the charge of the proton) with a tangential
velocity v. r is the radius of the orbit in which electron is revolving.
By Coulomb’s Law, the electrostatic force of attraction between the moving electron
and nucleus is
KZe 2
Coulombic force =
r2
1
K= (where o is permittivity of free space)
4 o
K = 9 109 Nm2 C–2
In C.G.S. units, value of K = 1 dyne cm2 (esu)–2
mv 2
The centrifugal force acting on the electron is
r
Since the electrostatic force balance the centrifugal force, for the stable electron orbit.
mv 2 KZe 2
= … (1)
r r2
KZe 2
(or) v2 = … (2)
mr
According to Bohr’s postulate of angular momentum quantization, we have
nh
mvr =
2
nh
v=
2 mr
n 2h 2
v2 = … (3)
4 2m 2r 2
Equating (2) and (3)
KZe 2 n 2h 2

mr 4 2 m 2 r 2
n 2h 2
solving for r we get r =
4π 2 mKZe 2
where n = 1,2,3 - - - - - 
Hence only certain orbits whose radii are given by the above equation are available for the
electron. The greater the value of n, i.e., farther the energy level from the nucleus the
greater is the radius.
The radius of the smallest orbit (n=1) for hydrogen atom (Z=1) is ro.
ro =
n 2h2
=

12  6.626  10 34  2
= 5.29 10–11 m = 0.529 Å

4 2 me 2 K 4  3.14   9  10
2 31

 1.6  10 
19 2
 9  10 9
Radius of nth orbit for an atom with atomic number Z is simply written as
n2
rn = 0.529  Å
Z
Calculation of energy of an electron
The total energy, E of the electron is the sum of kinetic energy and potential energy.
Kinetic energy of the electron = ½ mv2
 KZe 2
Potential energy =
r
KZe 2
Total energy = 1/2 mv2 – … (4)
r
From equation (1) we know that
mv 2 KZe 2
=
r r2
KZe 2
 ½ mv2 =
2r
Substituting this in equation (4)
KZe 2 KZe 2 KZe 2
Total energy (E) = – = 
2r r 2r
Substituting for r, gives us
2π 2mZ 2e 4K 2
E= where n = 1,2,3……….
n2h2
This expression shows that only certain energies are allowed to the electron. Since this
energy expression consist of so many fundamental constant, we are giving you the following
simplified expressions.
Z2
E = –21.8 10–12  erg per atom
n2
Z2 Z2
= –21.8 10–19  J per atom = –13.6  eV per atom
n2 n2
(1eV = 3.83 10–23 kcal
1eV = 1.602 10–12 erg

1eV = 1.602 10–19J)
Z2
E = –313.6  kcal / mole (1 cal = 4.18 J)
n2
The energies are negative since the energy of the electron in the atom is less than the
energy of a free electron (i.e., the electron is at infinite distance from the nucleus) which is
taken as zero. The lowest energy level of the atom corresponds to n=1, and as the quantum
number increases, E becomes less negative.
When n = , E = 0, which corresponds to an ionized atom i.e., the electron and nucleus are
infinitely separated.
H  H++ e– (ionisation).
Exercise 1: Find out the value of electrostatic potential energy of two electrons
separated by 3.0Å in vacuum./ Express your answer in joules and
electron volt.
Explanation for hydrogen spectrum by Bohr’s theory
According to the Bohr’s theory electron neither emits nor absorbs energy as long as it stays
in a particular orbit. However, when an atom is subjected to electric discharge or high
temperature, and electron in the atom may jump from the normal energy level, i.e., ground
state to some higher energy level i.e, exited state. Since the life time of the electron in
excited state is short, it returns to the ground state in one or more jumps.
During each jump, energy is emitted in the form of a photon of light of definite wavelength or
frequency. The frequency of the photon of light thus emitted depends upon the energy
difference of the two energy levels concerned (n1, n2) and is given by
 2 2 mZ 2 e 4 K 2  1 1
h = E2 – E1 =  2  2
 n 2 n1 
2
h
2 2 mZ 2 e 4 K 2  1 1
=   2 
 n1 n 2 
2
h3
The frequencies of the spectral lines calculated with the help of above equation are found to
be in good agreement with the experimental values. Thus, Bohr’s theory elegantly explains
the line spectrum of hydrogen and hydrogenic species.
Bohr had calculated Rydberg constant from the above equation.
c 22mZ 2e4K 2  1 1
= =  2  2
 h3
 n1 n 2 
1 22mZ 2e4K 2  1 1
  2  2
 h3c  n1 n 2 
22me 4K 2
where 3
= 1.097  10–7m–1 or 109678 cm–1
hc
i.e., Rydberg constant (R)
1 1 1
 ν = RZ2  2  2
λ  n1 n2 
e 4
According to quantum mechanics the Rydberg constant is given by R =
802h3C
Were  is reduced mass for the atom 0 is the permitivity of a vacuum. The reduced mass of
an atom with one electron is given by
mnuc  me
=
mnuc  me
where mnuc = mass of nucleus
and me = mass of electron. For a nucleus with mass mnuc  
 = me
and R = 109673 cm–1
Illustration 1: Find out the longest wavelength of absorption line for hydrogen gas
containing atoms in ground state.
1 1 1
Solution:  RZ 2  2  2 
  n1 n 2 
for longest wavelength E should be smallest i.e. transition occurs from
n = 1 to n = 2
n=7
n=6
n=5
n=4
n=3
n=2
n=1
1 1 1 
i.e. = 109673 cm–1  12   2 
 1 2 
1 3
 = 109673  cm–1
 4
4
= = 1.2157  10–5 cm = 121.6 nm
3  109673 cm 1
Exercise 2: i) The series limit for the Paschen series of hydrogen spectrum occurs at
8205.8Å. Calculate.
a) Ionization energy of hydrogen atom
b) Wave length of the photon that would remove the electron in the
ground state of the hydrogen atom.
ii) Calculate frequency of the spectral line when an electron from 5 th Bohr
orbit jumps to the second Bohr orbit in a hydrogen atom.
iii) Calculate the energy of an electron in 3rd Bohr orbit.
Illustration 2 Calculate the energy in kJ per mole of electronic charge accelerated by a

potential of 1 volt.
Solution: Energy in joules = charge in coulombs  potential difference in volt
= 1.6 10–19  6.02  1023  1
= 9.632  104 J or 96.32 kJ
Exercise 5: i) What is highest frequency photon that can be emitted from hydrogen
atom? What is wavelength of this photon?
ii) Calculate the longest wavelength transition in the Paschenseries of He+ .
iii) Calculate the ratio of the wavelength of first and the ultimate line of
Balmer series of Li2+?
Calculation of velocity
We know that
nh nh
mvr = ;v =
2 2mr
By substituting for r we are getting
2KZe 2
v=
nh
Where excepting n and z all are constants
Z
v = 2.18 108 cm/sec.
n
Further application of Bohr’s work was made, to other one electron species (Hydrogenic
ion) such as He+ and Li2+. In each case of this kind, Bohr’s prediction of the spectrum was
correct.
Merits of Bohr’s theory
i) The experimental value of radii and energies in hydrogen atom are in good agreement
with that calculated on the basis of Bohr’s theory.
ii) Bohr’s concept of stationary state of electron explains the emission and absorption
spectra of hydrogen like atoms.
iii) The experimental values of the spectral lines of the hydrogen spectrum are in close
agreement with that calculated by Bohr’s theory.
Limitations of Bohr’s theory
i) It does not explain the spectra of atoms having more than one electron.
ii) Bohr’s atomic model failed to account for the effect of magnetic field (Zeeman effect) or
electric field (Stark effect) on the spectra of atoms or ions. It was observed that when the
source of a spectrum is placed in a strong magnetic or electric field, each spectral line
further splits into a number of lines. This observation could not be explained on the basis
of Bohr’s model.
iii) De Broglie suggested that electrons like light have dual character. It has particle and
wave character. Bohr treated the electron only as particle.
iv) Another objection to Bohr’s theory came from Heisenberg’s Uncertainty Principle.
According to this principle “It is impossible to determine simultaneously the exact
position and momentum of a small moving particle like an electron”. The postulate
of Bohr, that electrons revolve in well defined orbits around the nucleus with well
defined velocities is thus not tenable.
Exercise 4: Calculate the de Broglie wavelength of an electron that has been

accelerated from rest through a potential difference of 1 KV.
Illustration 3: A series of lines in the spectrum of atomic hydrogen lies at wavelengths

656.46, 482.7, 434.17, 410. 29 nm. What is the wave length of next line in
this series.
Solution: The given series of lines are in the visible region and thus appears to be
Balmer series
Therefore n1 = 2 and n2 = ? for next line
If  = 410.29 10–7 cm and n1 = 2
n2 may be calculated for the last line
1 1 1

=R  n2  n2 
 1 2 
1 1 1
= 109673   2
410.29  10 7 2
2
n2 
n2 = 6
thus next line will be obtained during the jump of electron from 7th to 2nd
shell i.e,
1 1 1 1 1 

=R  22  72  = 109673  4  49 
   
 = 397.2 10–7 cm = 397.2 nm
Exercise 5: Calculate wavelength of photon emitted when an electron goes from n = 3

to n = 2 level of hydrogen atom.
Quantum Numbers
An atom contains large number of shells and subshells. These are distinguished from one
another on the basis of their size, shape and orientation (direction) in space. The
parameters are expressed in terms of different numbers called quantum numbers.
Quantum numbers may be defined as a set of four numbers with the help of which we can
get complete information about all the electrons in an atom. It tells us the address of the
electron i.e., location, energy, the type of orbital occupied and orientation
of that orbital.
i) Principal quantum number (n): It tells the main shell in which the electron resides and
the approximate distance of the electron from the nucleus. It also tells the maximum
number of electrons a shell can accommodate is 2n2, where n is the principal quantum
number.
Shell K L M N
Principal quantum number (n) 1 2 3 4
Maximum number of electrons 2 8 18 32
ii) Azimuthal or angular momentum quantum number (l): This represents the number
of subshells present in the main shell. These subsidiary orbits within a shell will be
denoted as 1,2,3,4,… or s,p,d,f… This tells the shape of the subshells. The orbital
angular momentum of the electron is given as
 h 
l l  1 h (or) l l  1  for a particular value of ‘n’  w here   . For a given
2  2 
value of n values of possible l vary from 0 to n – 1.
iii) The magnetic quantum number (m): An electron due to its angular motion around
the nucleus generates an electric field. This electric field is expected to produce a
magnetic field. Under the influence of external magnetic field, the electrons of a subshell
can orient themselves in certain preferred regions of space around the nucleus called
orbitals. The magnetic quantum number determines the number of preferred orientations
of the electron present in a subshell. The values allowed depends on the value of l, the
angular momentum quantum number, m can assume all integral values between –l to
+l including zero. Thus m can be –1, 0, +1 for l = 1. Total values of m associated with a
particular value of l is given by 2l + 1.
iv) The spin quantum number (s): Just like earth not only revolves around the sun but
also spins about its own axis, an electron in an atom not only revolves around the
nucleus but also spins about its own axis. Since an electron can spin either in clockwise
direction or in anticlockwise direction, therefore, for any particular value of magnetic
quantum number, spin quantum number can have two values, i.e., +1/2 and –1/2 or
these are represented by two arrows pointing in the opposite directions, i.e.,  and .
When an electron goes to a vacant orbital, it can have a clockwise or anti clockwise spin
i.e., +1/2 or –1/2. This quantum number helps to explain the magnetic properties of the
substances.
Shapes and size of orbitals
An orbital is the region of space around the nucleus within which the probability of finding an
electron of given energy is maximum (90–95%). The shape of this region (electron cloud)
gives the shape of the orbital. It is basically determined by the azimuthal quantum number l,
while the orientation of orbital depends on the magnetic quantum number (m). Let us now
see the shapes of orbitals in the various subshells.
s–orbitals: These orbitals are

y
spherical and symmetrical about the
nucleus. The probability of finding the
electron is maximum near the nucleus
and keep on decreasing as the
distance from the nucleus increases. 1s 2s
There is vacant space between two nucleus x
successive s–orbitals known as radial
node. But there is no radial node for
1s orbital since it is starting from the radial node
Z
nucleus.
The size of the orbital depends upon the value of principal quantum number(n). Greater the
value of n, larger is the size of the orbital. Therefore, 2s–orbital is larger than 1s orbital but
both of them are non-directional and spherically symmetrical in shape.
p–orbitals (l =1): The probability of finding the p–electron is maximum in two lobes on the
opposite sides of the nucleus. This gives rise to a dumb–bell shape for the p–orbital. For p–
orbital l = 1. Hence, m = –1, 0, +1. Thus, p–orbital have three different orientations. These
are designated as px,py & pz depending upon whether the density of electron is maximum
along the x y and z axis respectively. As they are not spherically symmetrical, they have
directional character. The two lobes of p–orbitals are separated by a nodal plane, where the
probability of finding electron is zero.
Y
X py pz
px
Z
The three p-orbitals belonging to a particular energy shell have equal energies and are
called degenerate orbitals.
d–orbitals (l =2): For d–orbitals, l =2. Hence m=–2,–1,0,+1,+2. Thus there are 5 d orbitals.
They have relatively complex geometry. Out of the five orbitals, the three (dxy, dyz,dzx) project
in between the axis and the other two dz 2 and d x 2  y 2 lie along the axis.
Z X
Y
d z2 d x2  y 2
Dough–nut shape or Baby Clover leaf shape

soother shape
X X Y
Y Z Z
dxz dyz
dxy
Rules for filling of electrons in various orbitals
The atom is built up by filling electrons in various orbitals according to the following rules.
Aufbau Principle: This principle states that the electrons are added one by one to the
various orbitals in order of their increasing energy starting with the orbital of lowest energy.
The increasing order of energy of various orbital is
1s,2s,2p,3s,3p,4s,3d,4p,5s,4d,5p,6s,4f,5d,6p,5f,6d,7p……………………
How to remember such a big sequence? To make it simple we are giving you the method
to write the increasing order of the orbitals. Starting from the top, the direction of the arrows
gives the order of filling of orbitals.
1s
2s 2p
3s 3p 3d
4s 4p 4d 4f
5s 5p 5d
6s 6p
7s
Alternatively, the order of increasing energies of the various orbitals can be calculated on
the basis of (n+l) rule.
The energy of an orbital depends upon the sum of values of the principal quantum number
(n) and the azimuthal quantum number (l). This is called (n+ l) rule.
According to this rule,
“In neutral isolated atom, the lower the value of (n+ l) for an orbital, lower is its
energy. However, if the two different types of orbitals have the same value of
(n+ l), the orbitals with lower value of n has lower energy’’.
Illustration of (n + l) rule
Values of
Type of orbitals Value of n Values of l Relative energy
(n+ l)
1s 1 0 1+0=1 Lowest energy
2s 2 0 2+0=2 Higher energy than 1s orbital
2p 2 1 2+1=3 2p orbital (n=2) have lower
3s 3 0 3+1=3 energy than 3s orbital (n=3)
Pauli’s Exclusion principle
According to this principle, an orbital can contain a maximum number of two electrons and
these two electrons must be of opposite spin.
Two electrons in an orbital can be represented by
 or 
Hund’s rule of maximum multiplicity
This rule deals with the filling of electrons in the equal energy (degenerate) orbitals of the
same sub shell (p,d and f). According to this rule,
“Electron pairing in p,d and f orbitals cannot occur untill each orbital of a given subshell
contains one electron each or is singly occupied”.
This is due to the fact that electrons being identical in charge, repel each other when
present in the same orbital. This repulsion can, however, be minimised if two electrons move
as far apart as possible by occupying different degenerate orbitals. All the electrons in a
degenerate set of orbitals will have same spin.
Illustration 4: Which hydrogen like ionic species has wavelength difference between the
first line of Balmer and first line of Lyman series equal to 59.3  10–9 m?
Neglect the reduced mass effect.
Solution: Wave number of first Balmer line of an species with atomic number Z is
given by
1 1
v   RZ 2  2  2 
1 2 
5RZ 2
v  ; Similarly wave number of v of first Lyman line is given by
36
1 1 3 1 1
v = RZ2  2  2  = RZ 2 ; v  and v  
1 2  4  
36 4 1  36 4  88
  –  =  = 2 
  =
5RZ 2
3RZ 2
RZ  5 3  15RZ 2
88
Z2 = = 9 or Z = 3  ionic species is Li2+
59.3  10  15  1.097  10 7
9
Electronic configuration of elements
Electronic configuration is the distribution of electrons into different shells, subshells and
orbitals of an atom .
Keeping in view the above mentioned rules, electronic configuration of any orbital can be
simply represented by the notation.]
Number of electrons in the

subshell
x
nl
Principal quantum number Symbol of subshell or
orbitals (s,p,d,f)
Alternatively
Orbital can be represented by a box and an electron with its direction of spin by arrow. To
write the electronic configuration, just we need to know (i) the atomic number (ii) the order in
which orbitals are to be filled (iii) maximum number of electrons in a shell, sub–shell or
orbital.
a) Each orbital can accommodate two electrons
b) The number of electrons to be accomodated in a subshell is 2  number of

degenerate orbitals.
Subshell Maximum number of electrons
s 2
p 6
d 10
f 14
c) The maximum number of electron in each shell (K,L,M,N…) is given by 2n2.

where n is the principal quantum number.
d) The maximum number of orbitals in a shell is given by n2 where n is the principal

quantum number.
e) The number of nodal planes associated with an orbital is given by l -1.
Importance of knowing the electronic configuration
The chemical properties of an element are dependent on the relative arrangement

of its electrons.
Illustration 5: Write the electronic configuration of nitrogen (atomic number= 7)
Solution:
1s2 2s2 2p3
    
Exceptional Configurations
Stability of half filled and completely filled orbitals
Cu has 29 electrons. Its expected electronic configuration is
1s22s22p63s23p64s23d9
But a shift of one electron from lower energy 4s orbital to higher energy 3d orbital will make
the distribution of electron symmetrical and hence will impart more stability.
Thus the electronic configuration of Cu is
1s2 2s22p63s23p64s13d10
Fully filled and half filled orbitals are more stable.

Illustration 6: We know that fully filled and half filled orbitals are more stable. Can you
write the electronic configuration of Cr(Z = 24)?.
Solution: Cr (Z = 24)
1s2, 2s2,2p6,3s2,3p6,4s1,3d5.
Since half filled orbital is more stable one 4s electron is shifted to 3d
orbital.
Exercise 6: 1st I.P. of nitrogen is higher than oxygen. Explain.
8. Dual Character
(Particle and Wave Character of Matter and Radiation)
In case of light some phenomenon like diffraction and interference can be explained on the
basis of its wave character. However, the certain other phenomenon such as black body
radiation and photoelectric effect can be explained only on the basis of its particle nature.
Thus, light is said to have a dual character. Such studies on light were made by Einstein in
1905.
Louis de Broglie, in 1924 extended the idea of photons to material particles such as
electron and he proposed that matter also has a dual character-as wave and
as particle.
Derivation of de-Broglie equation
The wavelength of the wave associated with any material particle was calculated by analogy
with photon.
In case of photon, if it is assumed to have wave character, its energy is given by
E = h ------------------ (i) (according to the Planck’s quantum theory)
where  is the frequency of the wave and ‘h’ is Planck’s constant
If the photon is supposed to have particle character, its energy is given by
E = mc2 ------------------ (ii) (according to Einstein’s equation)
where ‘m’ is the mass of photon, ‘c’ is the velocity of light.
By equating (i) and (ii)
h = mc2
But  = c/
c
h = mc2

(or)  = h /mc
The above equation is applicable to material particle if the mass and velocity of photon is
replaced by the mass and velocity of material particle. Thus for any material particle like
electron.
h
 = h/mv (or) =
p
where mv = p is the momentum of the particle.
9. Derivation of Angular Momentum from de Broglie

Equation
According to Bohr’s model, the electron revolves around the nucleus in circular orbits.
According to de Broglie concept, the electron is not only a particle but has a wave character
also.
If the wave is completely in phase, the circumference of the orbit

must be equal to an integral multiple of wave length ()
Therefore 2r = n
where ‘n’ is an integer and ‘r’ is the radius of the orbit
But  = h/mv
 2r = nh /mv
(or) mvr = n h/2
which is Bohr’s postulate of angular momentum, where ‘n’ is the principal

quantum number.
“Thus, the number of waves an electron makes in a particular Bohr orbit in one complete
revolution is equal to the principal quantum number of the orbit”.
Alternatively
2r 2r 2mvr

Number of waves ‘n’ = = =
 h mv h
where v and r are the velocity of electron and radius of that particular Bohr orbit in which
number of waves are to be calculated, respectively.
The electron is revolving around the nucleus in a circular orbit. How many revolutions
it can make in one second
Let the velocity of electron be v m/sec. The distance it has to travel for one revolution 2r,
(i.e., the circumference of the circle).
v
Thus, the number of revolutions per second is =
2r
Common unit of energy is electron volt which is amount of energy given when an electron is
accelerated by a potential of exactly 1 volt. This energy equals the product of voltage and
charge. Since in SI units coulombs  volts = Joules, 1 eV numerically equals the electronic
charge except that joule replaces coulombs.
Illustration 7: Two particles A and B are in motion. If the wavelength associated with
particle A is 5 10–8 m, calculate the wavelength associated with particle B
if its momentum is half of A.
Solution: According to de Broglie equation

h h
A = and B =
pA pB
A p
= B
B pA
But pB = ½ pA (given)
A 1/ 2p A
= =½
B pA
B = 2A = 2  510–8 m = 10–7 m
Illustration 8: Calculate the de Broglie wavelength of a ball of mass 0.1kg moving with a
speed of 60ms–1.
h 6.6  10 34
Solution:  =
mv 0.1  60
 = 1.1  10–34 m.
This is apparent that this wavelength is too small for ordinary observation.
Although the de Broglie equation is applicable to all material objects but it

has significance only in case of microscopic particles.
Since, we come across macroscopic objects in our everyday life, de

Broglie relationship has no significance in everyday life.
[Distinction between the wave- particle nature of a photon and the particle- wave
nature of a sub atomic particle]
Photon Sub Atomic Particle
1. Energy = h 1
Energy = mv2
2
c h
2. Wavelength = Wavelength =
 mv
[Note: We should never interchange any of the above]
10. Heisenberg’s Uncertainty Principle

All moving objects that we see around us e.g., a car, a ball thrown in the air etc., move along
definite paths. Hence their position and velocity can be measured accurately at any instant
of time. Is it possible for subatomic particle also?
As a consequence of dual nature of matter, Heisenberg, in 1927 gave a principle about the
uncertainties in simultaneous measurement of position and momentum (mass  velocity) of
small particles.
This principle states
“It is impossible to measure simultaneously the position and momentum of a small

microscopic moving particle with absolute accuracy or certainty” i.e., if an attempt is made to
measure any one of these two quantities with higher accuracy, the other becomes less
accurate.
The product of the uncertainty in position (x) and the uncertainty in the momentum (p =
m.v where m is the mass of the particle and v is the uncertainty in velocity) is equal to or
greater than h/4 where h is the Planck’s constant.
Thus, the mathematical expression for the Heisenberg’s uncertainty principle is simply
written as
x . p  h/4
Explanation of Heisenberg’s uncertainty principle

Suppose we attempt to measure both the position and momentum of an electron, to pinpoint
the position of the electron we have to use light so that the photon of light strikes the
electron and the reflected photon is seen in the microscope. As a result of the hitting, the
position as well as the velocity of the electron are disturbed. The accuracy with which the
position of the particle can be measured depends upon the wavelength of the light used.
The uncertainty in position is . The shorter the wavelength, the greater is the accuracy.
But shorter wavelength means higher frequency and hence higher energy. This high energy
photon on striking the electron changes its speed as well as direction. But this is not true for
macroscopic moving particle. Hence Heisenberg’s uncertainty principle is not applicable to
macroscopic particles.
Illustration 9: Why electron cannot exist inside the nucleus according to Heisenberg’s
uncertainty principle?
Solution: Diameter of the atomic nucleus is of the order of 10–15m

The maximum uncertainty in the position of electron is 10–15 m.
Mass of electron = 9.1 10–31 kg.
h
x. p =
4
x  (m.v) = h/4
h 1 6.63  10 34 1
v =  =  15
4 x.m
4
22 10  9.1 1031
7
v = 5.80  10 ms
10 –1
This value is much higher than the velocity of light and

hence not possible.
11. Quantum Mechanical Model of atom

The atomic model which is based on the particle and wave nature of the electron is known
as wave or quantum mechanical model of the atom. This was developed by Ervin
Schrodinger in 1926. This model describes the electron as a three dimensioinal wave in the
electronic field of positively charged nucleus. Schrodinger derived an equation which
describes wave motion of an electron. The differential equation is
d2 d2 d2 82m

   2 (E  V )  0
dx 2 dy 2 dz 2 h
where x, y, z are certain coordinates of the electron, m = mass of the electron E = total
energy of the electron. V = potential energy of the electron; h = planck’s constant and z
(psi) = wave function of the electron.
Significance of  The wave function may be regarded as the amplitude function expressed
in terms of coordinates x, y and z. The wave function may have positive or negative values
depending upon the value of coordinates. The main aim of Schrodinger equation is to give
solution for probability approach. When the equation is solved, it is observed that for some
regions of space the value of  is negative. But the probability must be always positive and
cannot be negative, it is thus, proper to use 2 in favour of .
Significance of 2: 2 is a probability factor. It describes the probability of finding an

electron within a small space. The space in which there is maximum probability of finding an
electron is termed as orbital. The important point of the solution of the wave equation is that
it provides a set of numbers called quantum numbers which describe energies of the
electron in atoms, information about the shapes and orientations of the most probable
distribution of electrons around nucleus.
12. Photo Electric Effect

Sir J.J. Thomson, observed that when a light of certain frequency strikes the surface of a
metal, electrons are ejected from the metal. This phenomenon is known as photoelectric
effect and the ejected electrons are called photoelectrons.
A few metals, which are having low ionisation energy like Cesium, show this effect under the
action of visible light but many more show it under the action of more energetic ultraviolet
light.
Light
electrons
+ –
Evacuated quartz tube
An evacuated tube contains two electrodes connected to a source of variable voltage, with
the metal plate whose surface is irradiated as the anode. Some of the photoelectrons that
emerge from this surface have enough energy to reach the cathode despite its negative
polarity, and they constitute the measured current. The slower photoelectrons are repelled
before they get to the cathode. When the voltage is increased to a certain value V o, of the
order of several volts, no more photoelectrons arrive, as indicated by the current dropping to
zero. This extinction voltage (or also referred as stopping potential) corresponds to the
maximum photoelectron kinetic energy i.e., eVo = ½ mv2
The experimental findings are summarised as below:
i) Electrons come out as soon as the light (of sufficient energy) strikes
the metal surface .
ii) The light of any frequency will not be able to cause ejection of electrons from a metal
surface. There is a minimum frequency, called the threshold (or critical) frequency, which
can just cause the ejection. This frequency varies with the nature of the metal. The
higher the frequency of the light, the more energy the photoelectrons have. Blue light
results in faster electrons than red light.
iii) Photoelectric current is increased with increase in intensity of light of same frequency, if
emission is permitted i.e., a bright light yields more photoelectrons than a dim one of the
same frequency, but the electron energies remain the same.
Light must have stream of energy particles or quanta of energy (h). Suppose, the threshold
frequency of light required to eject electrons from a metal is o, when a photon of light of
this frequency strikes a metal it imparts its entire energy (ho) to the electron.
E = ho E > ho
K.Emax = h – ho
K. E = 0
Metal
“This energy enables the electron to break away from the atom by overcoming the attractive
influence of the nucleus”. Thus each photon can eject one electron. If the frequency of light
is less than o there is no ejection of electron. If the frequency of light is higher than o (let it
be ), the photon of this light having higher energy (h), will impart some energy to the
electron that is needed to remove it away from the atom. The excess energy would give a
certain velocity (i.e, kinetic energy) to the electron.
h = ho + K.E
h = ho + ½ mv2
½ mv2 = h–ho
where,  = frequency of the incident light
o = threshold frequency
ho is the threshold energy (or) the work function denoted by  = ho (minimum energy of the
photon to liberate electron). It is constant for particular metal and is also equal to the
ionization potential of gaseous atoms.
The kinetic energy of the photoelectrons increases linearly with the frequency of incident
light. Thus, if the energy of the ejected electrons is plotted as a function of frequency, it
result in a straight line whose slope is equal to Planck’s constant ‘h’ and whose
intercept is ho.
K.E
of
Photoelectrons
Illustration 10: A photon of wavelength 5000 A strikes a metal surface, the work function of the
metal being 2.20 eV. Calculate (i) the energy of the photon in eV (ii) the kinetic
energy of the emitted photo electron and (iii) the velocity of the photo electron.
Solution: i) Energy of the photon
E = h =
hc
=
 
6.6  10 34 Js 3  108 ms 1 
= 3.96  10–19 J
7
 5  10 m
1 eV = 1.6  10 J
–19
3.96  10 19 J
Therefore E = = 2.475 eV
1.6  10 19 J / ev
ii) Kinetic energy of the emitted photo electron

Work function = 2.20 eV
Therefore, KE = 2.475 – 2.20 = 0.275 eV = 4.4  10–20 J
iii) Velocity of the photo electron

1
KE = mv 2 = 4.4  10–20 J
2
2  4.4  10 20
Therefore, velocity (v) = = 3.11  105 ms–1
9.1 10  31
13. Solution to Exercises

KZe 2
Exercise 1: E=
r
1
K= = 9  109 Nm2 C–2
4 0
9  10 9  1  (1.6  10 19 ) 2
= = 7.68  10–19J
3  10 10
 1 eV = 1.6  10–19J
7.68  10 19
E= = 4.8 eV
1.6  10 19
6.626  10 34  3  10 8
Exercise 2: i) a) Energy corresponding to 8205.8 Ao =
8205 .8  10 10
= 2.422 × 10-19 J = 1.572 eV
1 1
ΔE  E1H  Z 2  2  2 
 n1 n 2 
 1 1 
1.512 eV = E1H × (1)2 ×  2  2 
3  
E 1H
1.512 eV =
9
E1 H = 13.608 eV
 Ionisation energy of hydrogen atom = 13.6 eV
hc 6.626  10 34  3  10 8
b)   
E 13.6  1.602  10 19
= 916 Ao
1 1 1 1 1
ii) = R  2  2  = 109673  2  2  = 2.304 106 m–1
  n1 n 2  2 5 
C
v= = 2.304  106 m–1  2.998 108 m/s

= 6.906  1014 Hz
13.6
iii) En =  eV
n2
13.6
=  2 = – 1.51 eV
3
= – 2.42  10–19 J
Exercise 3: i) Highest frequency photon is emitted when electron comes from infinity
to 1st energy level.
13.6Z 2
E=  = – 13.6eV
12
or 13.6  1.6  10–19 Joule = 2.176  10–18 Joule
E = h
E 2.176  10 18 J
v= = = 0.328  1016 Hz
h 6.626  10  34 JS
C 3  10 8
v= = = 9.146  10–8 m
 0.328  10 16
1 1
ii)   RH  Z 2  2  2 
 n1 n 2 
For He; Z = 2; For Paschen series n1 = 3
For longest wavelength n2 = 4
 1 1 1 1 
 109678  2   2  2  = 109678×4×    = 109678 ×4×
1 2 7
 3 4   9 16  144
 = 4689 Ao
iii) Wave number of first line of Balmer,
 1 1  5  9R 5R
 1 = RZ 2  2  2   
2 3  36 4
4
wave length of first line of Balmer =
5R
 1 1 9R
wave number of ultimate line of Balmer,  2 = RZ 2  2   =
2  4
4
wave length of ultimate line of Balmer =
9R
9
Ratio =
5
Exercise 4: Energy in Joules = Charge on the electron in coloumb  pot. diff. in volts.
= 1.609 10–19 1000 = 1.609 10–16 J
Kinetic energy (1/2 mv2) = 1.609 10–16 J
1
9.1 10–31 v2 = 1.609 10–16
2
v2 = 3.5361014
v = 1.88 107 ms–1
h = 6.626 10–34 J sec
h 6.626 10 34
= = = 3.87 10–11 m.
mv 9.1 1031  1.88  107
1 1 1
Exercise 5:  RZ 2  2  2 
  n1 n 2 
1 1 1
  109673  12  2  2 
 2 3 
5
= 109673 
36
36
= = 6.56  10–7 m or 656 nm
109673  5
Exercise 6: Due to presence of half filled orbital in nitrogen which impart it extra
stability.
14. Solved Problems
14.1 Subjective
Problem 1: Calculate the wavelength emitted during the transition of electron in between
two levels of Li2+ ion whose sum is 4 and difference is 2.
Solution: Let the transition occurs between the level n1 and n2 and n2  n1
Given that n1 + n2 = 4
n2 – n1 = 2
 n1 = 1 and n2 = 3
1  1 1  8 
Therefore,  R h  Z 2  2  2
= 109678  (3)2  
  (1) (3 )  9 
  = 1.14  10–6 cm
Problem 2: Find the quantum number ‘n’ corresponding to the excited state of He + ion if on
transition to the ground state that ion emits two photons in succession with
wavelengths 108.5 and 30.4 nm.
Solution: 2= 30.4  10–7 cm

2 = 108.5  10–7 cm
Let excited state of He+ be n2. It comes from n2 to n1 and then from n1 to 1 to
emit two successive photon.
1  1 1
 RH Z 2  2  2 
2  (1) n1 
1  1 1 
 = 109678  (2)2  2  
30.4  10 7  (1) (n1 ) 2 
n1 = 2
Now for , n1 = 2, n2 = ?
1  1 1 
7
 10.9678  4 2  
108.5  10  (2) (n 2 ) 2 
 n2 = 5
Hence excited state for He is 5th orbit.
Problem 3: The Lymann series of the hydrogen spectrum can be represented by the
equation.
 1 1 
 = 3.2881  1015 s–1  2
 
 (1) (n) 2 
(where n = 2, 3,…..)
Calculate the maximum and minimum wavelength of lines in this series.
1  3.2881  10 15 1  1 1
Solution:    m  2  2
 c 3  10 8
 (1) n 
1
Wavelength is maximum (  min ) when n is minimum so that is maximum
n2
1 3.2881  10 15  1 1 
  min    2  
 max 3  10 8  (1) (2) 2 
3  10 8 4
 max = 
3.2881  10 15
3
= 1.2165  10–7 m = 121.67 nm
Wavelength is minimum ( max ) when n is 
i.e. series converge
1 3.2881  10 15
  max  
 min 3  10 8
 min = 0.9124 10–7 m 91.24 nm
Problem 4: When certain metal was irradiated with light frequency 1.6 1016 Hz the photo
electrons emitted had twice the kinetic energy as did photo electrons emitted
when the same metal was irradiated with light frequency 1.0  1016 Hz.
Calculate threshold frequency (v0) for the metal.
Solution: hv = hv0 + KE
KE1 = h(v1 – v0)
KE 1
KE2 = h(v2 – v0) =
2
v  v0 1 1.0  10 16  v 0 1
 2     v0 = 4  1015Hz
v1  v 0 2 1.6  10 16  v 0 2
Problem 5: Iodine molecule dissociates into atoms after absorbing light of 4500Å. If one
quantum of radiation is absorbed by each molecule, calculate the kinetic
energy of iodine atoms. (Bond energy of I2 = 240 kJ (mol).
Solution: Energy given to iodine molecule

hc 6.625  10 34  3  10 8
 = 4.417  10–19J
 4500  10 10
Also energy used for breaking up
240  10 5
I2 molecule = = 3.984  10–19J
6.023  10 23
 Energy used in imparting kinetic to two atoms

= (4.417 – 3.984)  10–19J
( 4.417  3.984 )
 KE of iodine atom =  10 19 = 0.216 10–19J
2
Problem 6: Two hydrogen atoms collide head on and end up with zero kinetic energy. Each
atom then emits a photon of wavelength 121.6 nm. Which transition leads to
this wavelength? How fast were the hydrogen atoms travelling before
collision?
Solution: Wavelength is emitted in UV region and thus n1 = 1
1 1 1
For H atom =  RH  2  2 
 1 n 
1 1 1
 9
 1.097  10 7  2  2 
121.6  10 1 n 
n=2
Also the energy released is due to collision and all the kinetic energy is
released in form of photon.
1 hc
 mv 2 
2 
1 6.625  10 34  10 3
  1.67  10 27  v 2 
2 121 .6  10 9
 v = 4.43  104 m/sec
Problem 7: Find out the angular momentum of an electron in

a) 4s orbital
b) 3p orbital
c) 4th orbital
h
Solution: Angular momentum in an orbital = (  1)
2
i)  = 0 for 4s orbital, hence orbital angular momentum = 0
ii)  = 2 for 3p orbital
h h
 angular momentum = (1  1)  1 =
2 2
iii) Angular momentum in an orbit
nh 4h 2h
=  
2 2 
Problem 8: Given below are the sets of quantum numbers for given orbitals. Name these
orbitals.
i) n = 2,  = 1, m = –1
ii) n = 4,  = 2, m = 0
iii) n = 3,  = 1, m = ± 1
iv) n = 4,  = 0, m = 0
v) n = 3,  = 2, m = ± 2
Solution: i) 2px or 2py

ii) 4dz2
iii) 3px or 3py
iv) 4s
v) 3d x 2  y 2 or 3d xy
Problem 9: A compound of vanadium has a magnetic moment of 1.73 BM work out the
electronic configuration of the vanadium in the compound.
Solution: Magnetic moment = n(n  2)

Where n is number of unpaired electrons
 1.73 = n(n  2) or (1.73)2= n 2 + 2n, n = 1
Vanadium atom must have the unpaired electron and thus its configuration is:
4+ 2 2 6 2 6 1
23V : 1s 2s 2p 3s 3p 3d
Problem 10: An electron beam can undergo defraction by crystals. Through what potential
should a beam of electrons be accelerated so that its wavelength becomes
equal to 1.54Å.
Solution: For an electron

1
mu2 = eV
2
(Where V is accelerating potential)
h
=
mu
2
1  h 
 m   eV
2  m 
1 h2 1 (6.625  10 34 ) 2
V=  = = 63.3 volt
2 m2 e 2  9.108  10 31  (1.54  10 10 ) 2  1.602  10 19
14.2 Objective
Problem 1: For a delectron, the orbital angular momentum is:

(A) 6 (B) 2
(C)  (D) 2
Solution: For delectron,  =2, orbital angular momentum

= (  1)  2(2  1)  6
 (A)
Problem 2: If the nitrogen atoms had electronic configuration 1s 7, it would have energy
lower than that of the normal ground state configuration 1s 2 2s2 2p3 because
the electrons would be closer to the nucleus. Yet 1s 7 is not observed because
it violates
(A) Heisenberg’s uncertainity principle
(B) Hund’s rule
(C) Pauli exclusion principle
(D) Bohr’s postulate of stationary orbits
Solution: According to Pauli’s exclusion principle, an orbital cannot have more than two
electrons and these two with opposite spin.
(C)
Problem 3: The energy of an electron in the first Bohr orbit of H atom is – 13.6 eV. The
possible energy value(s) of excited state(s) for electron in Bohr orbitls of
hydrogen is are
(A) – 3.4 eV (B) – 4.2 eV
(C) 6.8 eV (D) +6.8 eV
 13.6
Solution: En  eV
n2
 13.6
When n = 2, E2 =  3.4eV
4
Problem 4: The electronic configuration of an element is 1s2 2s2 2p6, 3s2, 3p6, 3d5, 4s1. This
represents its
(A) Excited state (B) Ground state
(C) Cationic form (D) Anionic from
Solution: The given electronic configuration is ground state for chromium.

 (B)
Problem 5: Which of the following sets of quantum number is./are not permitted?
3 1
(A) n = 3,  = 3, m = 0, s = (B) n = 3,  = 2, m = 2, s = –
2 2
1 1
(C) n = 3,  = 1, m = 2, s = – (D) n = 3,  = 0, m = 0, s = +
2 2
Solution: When n = 3,  cannot be 3. so (A) is not permitted when  = 1, m cannot
be = –2.
So (C) is not permitted

 (A) and (C)
Problem 6: Which of the following pairs of ions have the same electronic configuration?
(A) Cr3+, Fe3+ (B) Fe3+, Mn2+
3+ 3+
(C) Fe , Co (D) Se3+, Cr3+
Solution: Fe3+ and Mn2+ have same electronic configuration

 (B)
Problem 7: If an electron in Hatom has an energy of – 78.4 kcal/mol. The orbit in which the
electron is present is:
(A) 1st (B) 2nd
(C) 3rd (D) 4th
 313 .6  313 .6
Solution: En = kcal/mol  – 78.4 = n=2
n2 n2
Problem 8: What transition in the hydrogen spectrum would have the same wavelength as
the Balmer transition, n = 4 to n = 2 in the He+ spectrum.
(A) n = 4 to n = 2 (B) n = 3 to n = 2
(C) n = 3 to n = 1 (D) n = 2 to n = 1
1  1 1  3
Solution:   2  2 R
 2 4  4
In Hspectrum for the same  or  as Z = 1, n = 1, n2 = 2
 (D)
Problem 9: Principal. Azimuthal and magnetic quantum numbers are respectively

related to
(A) Size, orientation and shape (B) Size shape and orientation
(C) Shape, size and orientation (D) None of these
Solution: Principal gives ie, azimuthal gives shape and magnetic quantum number
gives the orientation
 (B)
Problem 10: If the radius of 2nd Bohr orbit of hydrogen atom is r2. The radius of third Bohr
orbit will be
4
(A) r2 (B) 4r2
9
9
(C) r2 (D) 9r2
4
n 2h 2 r2 2 2 9
Solution: r   2  r3 = r 2
4 2 mZe 2 r3 3 4
 (C)
15. Assignments
15.1 Subjective problems
LEVEL – I
1. Calculate the longest wavelength in the Paschen series of He+ion.
2. Calculate the ratio of the wavelength of first and the ultimate line of Balmer series
of Li2+.
3 Calculate the number of photons emitted in 10 hours by a 60 W sodium lamp

( = 5893Å).
4. An electron collides with a hydrogen atom in its ground state and excited it to a state
of n=3. How much energy was given to the hydrogen atom in this inelastic collision?
5. Hydrogen atom in states of high quantum number have been created in the
laboratory and observed in space.
a) find the quantum number of the Bohr orbit in a H–atom whose radius is
0.0100 mm ?
b) what is the energy of H–atom in this state?
6. With what velocity should an –particle travel towards the nucleus of a copper atom
so as to arrive at a distance 10–13 metre from the nucleus of
the copper atom.
7. An electron beam can undergo diffraction by crystals. Through what potential should
a beam of electrons be accelerated. So that its wave length becomes equal
to 1.54 Å.
8. If the uncertainty in position and momentum are equal. Calculate the uncertainty in
velocity for an electron.
9. Calculate the kinetic energy of an electron emitted from the surface of a metal by
light of wavelength 5.510–8 cm. Threshold energy for the metal is
2.6210–9 ergs.
10. Suppose 10–17J of energy is needed by the interior of human eye to see an object.
How many photons of green light (=550 nm) are needed to generate this minimum
amount of energy?
LEVEL – II
1. The power output for a certain laser transition was found to be 2.79 watt per square
meter. Given  = 520 nm, calculate the number of quanta emitted per square meter
per second.
2. An electron in a hydrogen like atom is in an excited state. It has a total energy of

–3.4 eV. Calculate (i) kinetic energy and (ii) de-Broglie wavelength of the electron.
3. Light from a discharge tube containing hydrogen atoms falls on the surface of a
piece of sodium. The kinetic energy of the fastest photo electrons emitted from
sodium is 0.73 eV. The work function for sodium is 1.82 eV. Find
a) The energy of the photons causing the photo electric emission?
b) The quantum numbers of the two levels involved in the emission of these
photons?
4. Find the threshold wavelengths for photoelectric effect from a copper surface, a
sodium surface and a caesium surface? The work function of these metals are 4.5
eV, 2.3 eV and 1.9 eV respectively.
5. Calculate
a) The de-Broglie wavelength of an electron moving with a velocity of 5.0 × 105 ms–1
and
b) Relative de-Broglie wavelength of an atom of Helium and an atom of oxygen
moving with same velocity (h = 6.63 × 10––34 kg m2 sec–1).
6. The series limit for the Paschen series of hydrogen spectrum occurs at 8205.8Å.
Calculate.
a) Ionization energy of hydrogen atom
b) Wave length of the photon that would remove the electron in the ground state of
the hydrogen atom.
7. The angular momentum of an electron in a particular orbit of Li2+ion is 5.2728 × 10–34

kg m2/sec. Calculate the frequency of the spectral line when electron falls from this
level to the level where angular momentum of electron will be 3.1636 × 10–34 kg
– m2/sec.
8. The electron energy in hydrogen atom is given by E = 21.7  10–12/ n2 ergs. Calculate
the energy required to remove an electron completely from n = 2 orbit. What is the
longest wavelength (in cm) of light that can be used to cause this transition?
9. The wavelength corresponding to a transition when electron falls from a certain

quantum level to the ground state of an He+ ion is 24.31 nm. Find the ratio of velocity
of the electron in the next quantum level to that of velocity of light?
10. Calculate the energy emitted when electron of 1.0 g atom of hydrogen undergo
transition giving the spectral lines of lowest energy in u.v. region of its atomic
spectrum.
(RH = 1.1  107 m–1, c = 3  108 ms–1, h = 6.62  10–34 J–sec)
15.2 Objective
LEVEL – I
1. If the electronic structure of oxygen atom is written as 1s2 2s2 2p4 it would violate
(A) Hund’s rule (B) Paulis exclusion principle
(C) Both Hunds’ and Paulis’ principles (D) None of these
2. Number of nodal planes for f-orbital are

(A) 3 (B) 2
(C) 1 (D) 0
3. One Bohr magneton equals

ehc ec
(A) (B)
4n 4hm
hc eh
(C) (D)
me 4  4mc
4. Three isotopes of an element have mass numbers M, (M + 1) and (M + 2). If the

mean mass number is (M + 0.5) than which of the following ratio may be accepted
for M, (M + 1), (M + 2) in that order.
(A) 1 : 1 : 1 (B) 4 : 1 : 1
(C) 3 : 2 : 1 (D) 2 : 1 : 1
5. A possible set of quantum numbers for the last electron added to a gallium atom
(Z = 31) in its ground state is
n l m mS
(A) 4 1 –1 +1/2
(B) 4 0 0 –1/2
(C) 3 2 +2 +1/2
(D) 3 0 0 –1/2
6. The angle made by angular momentum vector of an electron with z axis is given by
(A) cos = l/m (B) cos = l/m
(l  1) m
(C) cos  = (D) cos =
m l(l  1)
7. The distance between 3rd and 2nd orbit of hydrogen atom is

(A) 2.646 10–8 cm (B) 2.116 10–8 cm
(C) 1.058 10–8 cm (D) 0.529  10–8 cm
8. An atom has four unpaired electrons. The total spin of this atom will be
(A) 1 (B) 1.5
(C) 2 (D) 4
9. For a ‘d’ electron, the orbital angular momentum is

(A) 6 (B) 2
(C)  (D) 2
10. Which of the following pairs can form correct set of isosters ?
(A) MgS, CaF2 (B) C6H6, B3N3H6
(C) CO, N2O (D) All the above
11. Electromagnetic radiation (Photon) with least wavelength result when an electron in
the hydrogen atom falls from n = 5 to
(A) n = 1 (B) n = 2
(C) n = 3 (D) n = 4
12. The first five ionization energies of an element are 801, 2428, 3660, 25030, 32835 in
kJ/mol. Then the element could be
(A) a halogen (B) a noble gas
(C) a third group element (D) a second group element
13. The energy required to melt 1g ice is 33J. The number of quanta of radiation of
frequency 4.67 1013 sec–1, that must be absorbed to melt 10 g ice is
(A) 1.065 1022 (B) 3.205 1023
(C) 9.076 1020 (D) none of these
14. If the wave length of first line of the Balmer series of hydrogen atom is 656.1 nm, the
wave length of second line of this series would be
(A) 218.7 nm (B) 328.0 nm
(C) 486.0 nm (D) 640.0 nm
15. The energy of an electron in the first Bohr orbit for He + ion is –54.4 eV. Which one of
the following is a possible excited state for electron in Bohr orbit of He+ ion?
(A) –6.04 eV (B) – 6.8eV
(C) – 1.7 eV (D) +1.36 eV
16. The outermost electronic configuration of the most electronegative element is

(A) ns2,np3 (B) ns2,np4
2 5
(C) ns ,np (D) ns2,np6
17. The first four ionization energies of an element are 191, 578,872 and 5962 kcal. The
number of valence electrons in the element is
(A) 1 (B) 2
(C) 3 (D) 4
18. The quantum numbers of +1/2 and –1/2 for the electron spin represent
(A) Rotation of the electron in clockwise and anticlockwise direction respectively
(B) Rotation of the electron in anticlockwise and clockwise direction respectively
(C) Magnetic moment of the electron pointing up and down respectively
(D) Two quantum mechanical spin states which have no classical analogue.
19. A atom forms an ion by the loss of three electrons. The ion has an electronic
configuration [Ar]3d6. The symbol of the ion is
(A) Fe3+ (B) Ni3+
3+
(C) Co (D) Mn+3
20. Given that in H–atom, the transition energy for n=1 to n=2 is 10.2 eV, the energy for
the same transition in Be3+ is
(A) 20.4 eV (B) 30.6 eV
(C) 40.8 eV (D) None of these
LEVEL – II
1. When alpha particles are sent through a thin metal foil, most of them go straight through the
foil because:
(A) alpha particles are much heavier than electrons
(B) alpha particles are positively charged
(C) most part of the atom is empty space
(D) alpha particle move with high velocity
2. Which represent a possible arrangement ?
n  m s
(A) 3 2 –2 1/2
(B) 4 0 0 1/2
(C) 3 2 –3 1/2
(D) 5 3 0 ½
3. Which set of quantum number is consistent with theory

(A) n = 2,  = 1, m = 0, s = –1/2 (B) n = 4,  = 3, m = 2, S = –1/2
(C) n = 3,  = 2, m = 3, S = +1/2 (D) n = 4,  = 3, m = 3, S = +1/2
4. Which of the following statements are false:
(A) The uncertainty in position and momentum in Heisenberg’s principle due to electron
wave.
(B) The energy level order 4s < 3d < 4p < 5s may not hold good for all elements
(C) The quantum nature of light radiation is manifested in photoemission of electrons
(D) According to Bohr’s theory the energy decreases as n increases.
5. Five valence electrons of 15P are labeled as
Pq x y z
3s 3P
If the spin quantum number of q and z is + 1/2
The group of electrons with three of the quantum number same are :
(A) Pq (B) (xyz), (pq)
(C) (pq), (xyz), (pz) (D) (pq), (xyz), (qy)
6. Which of the following is/are correct?
(A) the energy of an electron depends only on the principal quantum numbers not on the
other quantum numbers
(B) the energy of an electron depends only on the principal quantum number in case of
hydrogen and hydrogen like atoms.
(C) The difference in potential energies of any two energy level is always more than the
difference in kinetic energies of these two levels.
(D) An electron in an excited state can always emit a photon or two but can not absorb a
photon
7. The ratio of the e/m values of a proton and a -particle is
(A) 2 : 1 (B) 1 : 1
(C) 1 : 2 (D) 1 : 4
8. Let An be the area enclosed by the nth orbit in a hydrogen atom. The graph of ln(An/A1)
against ln(n):
(A) will pass through origin
(B) will be straight line with slope = 4
(C) will be a monotonically increasing non-linear curve
(D) will be a circle
9. Which of the following is the nodal plane of dxy orbital ?

(A) XY (B) YZ
(C) ZX (D) all
10. Ground state electronic configuration of nitrogen atom can be represented by

(A) (B)
(C) (D)
COMPREHENSION
WRITE-UP I
For hydrogen atom or 1-electron ions, the wave functions of 1s and 2s atomic orbitals are given as
under:
Zr
1 
1s   e a0
a03
1/ 2
 Z   Zr   a
Zr
 2s   2  e 0
 2a0   a0 
The wave functions for any 1-electron system is given by

 = k e–kr where k and k are constants.
The number of angular nodes are given by the value of angular quantum number and angular node
is directional in nature. Total number of nodes is nothing but it is the sum of radial nodes (n – – 1)
and angular nodes ().
On the basis of the above write up, answer the following questions.
1. Which of the following is the correct representation of plot radial function (r.f.) in Y-axis vs
distance from the nucleus in X-axis for 1-elelectron of 3p-atomic orbital?
Y Y
(A) (B)
r.f.
r.f.
r X r X
Y Y
(C) (D)
r.f.
r.f.
r X r X
2. If the nodes at infinity is not neglected, then what is the total number of radial and angular
nodes of 3px-orbitals?
(A) 4 (B) 3
(C) 5 (D) infinity
3. The distance from the nucleus of the radial nod of 2s-electron of Li2+ ion (a0 = Bohr’s radius
is equal to
(A) 0.67a0 (B) 2a0
(C) a0 (D) 0.5a0
WRITE-UP II
According to Bohr’s theory, when electron jumps from higher orbit of lower orbit, then it
radiates energy in the form of electromagnetic radiations and provides emission spectrum. If
 E = En2  En1
1 1
E  13.6  Z2  2  2  eV/atom
 n1 n2 
1 1 1
    RH  Z2  2  2  eV / atom …(i)
  n1 n2 
where RH is Rydberg’s constant and RH = 107 m–1
So far in Bohr’s theory, we have assumed that nucleus is at rest and the electron is
revolving around it. The assumption of nucleus to be at rest is entirely valid if an only if the
mass of nucleus is infinite.
So far, for the finite mass of the nucleus, both the nucleus and the electron will revolve
around the common centre of mass which lies on the line connecting the two particles.
Thereby Bohr’s theory (i.e. expression for energy, Rydberg’s constant, etc.) needs to be
modified. So Rydberg’s constant of Ritz equation (i) needs to be modified. Simply the mass
of electron i.e., me has to be replaced by reduced mass () which is related as:
= 1 1  1
 mN me
where mN = mass of nucleus
me = mass of electron
Keep in mind that the minimum amount of energy needed to remove electron or carry out
electron from ground state to infinite from gaseous and isolated atom, is known as ionization
energy.
4. What will be the value of modified Rydberg’s constant, if the ratio of mass of nucleus to the
mass of electron is 3:2
3 5
(A)  107 m1 (B)  107 m1
5 3
2 8
(C)  107 m1 (D)  107 m1
5 5
5. If the mass of the nucleus be 5 times than that of the mass of electron and both the nucleus
and the electron revolves around the common centre of mass which lies on the same line
connecting the two spheres; then what will be the wave length of the transition of 1 st line of
Balmer series for He+ ion ?
(A) 8.64  10–7m (B) 1.1  10–7m
(C) 2.16  10 m
–7
(D) 3.5  10–7m–1
6. If the ratio of mass of electron to mass of nucleus be 1:1 and both the nucleus and the
electron revolve around the common centre of mass which lies on the same line connecting
the two; then what will be the value of ionization energy for Li2+ ions? Given that I.P. of H-
atom is 13.6eV/atom.
(A) 61.2 eV (B) 13.6 eV
(C) 54.4 eV (D) 6.8 eV
MATCH THE COLUMN

1. Match the following
LIST  I LIST  II
(A) h (p) dorbital.
Orbital angular momentum = 2
2
(B) nh (q) Classical analogue of angular
mvr  , n  1,2,3.... momentum.
2
(C) Orbital with five fold degeneracy but (r) porbital
four lobes
(D) Nshell (s) No. of waves made by electron is 4.
2. Match the List – I and List – II.

List – I List - II
(A) Radius of nth orbit (p) inversely proportional to n2
(B) Energy of nth Shell (q) Integral Multiple of h/2
(C) Angular momentum of electron (r) Proportional of n2
(D) Velocity of electron in nth orbit (s) Inversely proportional to ‘n’
16. Hints to Subjective Assignments

LEVEL – I
1. Longest wavelength is associated with least energy.

3. Total energy emitted = number of photons emitted × energy of 1 photon
6. At the closest distance of approach, the alpha particle will have the same kinetic and
potential energies
LEVEL – I
2. a) KE for a H – like atom is same as the magnitude of total energy

5. b)   1/m if the velocity is same.
7. Use quantization condition for a Bohr orbit in order to evaluate the n values.
17. Answers
17.1 Subjective
LEVEL – I
1. 4689Å 2. 9/5
3. 6.4 × 1024 4. 12.08 eV
5. a) 435; b) –7.18  10–5 ev
6. 6.3 × 106m/sec 7. 63.40
8. 7.98 ×1012 m/sec 9. 9.93  10–10 ergs
10. 28
LEVEL – II
1. 7.30 × 1018 2. i) 3.4 eV; ii) 6.654Å

3. a) 2.55 eV b) 2  4
4. For Cu = 276 nm; For Mg = 540 nm; For Cs = 654 nm
5. a) 1.46 × 10–9 m; b)  for He is 4 times greater than the  of oxygen atom
6. a). I.P. = 13.6 eV; b)  = 916Å 7. 2.1058 × 1015
8. 5.42  10–12 ergs, 3.67  10–5 cm 9. 1:344
10. 978.75 kJ mole–1
17.1 Objective
LEVEL – I
1. (D) 2. (A)
3. (D) 4. (B)
5. (A) 6. (D)
7. (A) 8. (C)
9. (A) 10. (B)
1. (A) 2. (C)
3. (A) 4. (C)
5. (A) 6. (C)
7. (C) 8. (D)
9. (C) 10. (D)
LEVEL – II
1. (A), (C) 2. (A), (B), (D)
3. (A), (B), (D) 4. (B), (D)
5. (A), (B) 6. (B), (D)
7. (A), (B) 8. (A),(B),(C)
9. (B), (C) 10. (A), (D)
COMPREHENSION
1. (D) 2. (B)
3. (A) 4. (A)
5. (C) 6. (A)
MATCH THE COLUMN

1. (A - R), (B - Q), (C – P), (D - S) 2. (A – R), (B – P), (C - Q), (D - S)

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RSM79PhIASCH1

2. Dalton’s Atomic Theory

The main postulates of Dalton’s atomic theory are

We know that an atom is electrically neutral, if it contains negatively charged electrons it

Characteristics of the three fundamental particles are:

Approximate relative mass 1/1836 1 1

Approximate relative charge –1 +1 No charge

Mass in kg 9.10910–31 1.67310–27 1.67510–27

Mass in amu 5.48510–4 1.007 1.008

Actual charge (coulomb) 1.60210–19 1.60210–19 0

Actual charge (e.s.u.) 4.8  10–10 4.8  10–10 0

3.1 Thomson’s Model

3.2 Rutherford’s Model

– particles emitted by radioactive substance were shown to be dipositive Helium ions

ii) Most of the space outside the nucleus is empty.

Defects of Rutherford’s atomic model

2. Stability of the atom: Neils Bohr pointed out that Rutherford’s

1 amu = 1.66 10–27 kg = 931.5 MeV

4. Some Important Characteristics of a Wave

The frequency of a wave is inversely proportional to its wave length ()

iv) Wave number   : It is defined as number of wavelengths per cm. It is denoted by

Wavelengths of electromagnetic radiations

Series n1 n2 Main spectral lines

Lyman 1 2,3,4, etc Ultra – violet

Balmer 2 3,4,5 etc Visible

Paschen 3 4,5,6 etc Infra – red

Brackett 4 5,6,7 etc Infra – red

Pfund 5 6,7,8, etc Infra – red

The pattern of lines in atomic spectrum is characteristic of hydrogen.

Types of Emission spectra

6. Planck’s quantum theory

i) Substances radiate or absorb energy discontinuously in the form of small packets or

iv) A body can radiate or absorb energy in whole number multiples of a

Neils Bohr used this theory to explain the structure of atom.

7. Bohr’s Atomic Model

 Ordinarily an electron continues to move in a particular stationary state without losing

 If energy is supplied to an electron, it may jump (excite) instantaneously from lower

Energy absorbed or released in an electron jump, (E) is given by

Radius and Energy levels of hydrogen atom

= 5.29 10–11 m = 0.529 Å

Calculation of energy of an electron

1eV = 1.602 10–12 erg

Explanation for hydrogen spectrum by Bohr’s theory

Bohr had calculated Rydberg constant from the above equation.

Illustration 2 Calculate the energy in kJ per mole of electronic charge accelerated by a

Solution: Energy in joules = charge in coulombs  potential difference in volt

= 1.6 10–19  6.02  1023  1

= 9.632  104 J or 96.32 kJ

Merits of Bohr’s theory

Limitations of Bohr’s theory

Exercise 4: Calculate the de Broglie wavelength of an electron that has been

Illustration 3: A series of lines in the spectrum of atomic hydrogen lies at wavelengths

Therefore n1 = 2 and n2 = ? for next line

If  = 410.29 10–7 cm and n1 = 2

n2 may be calculated for the last line

Exercise 5: Calculate wavelength of photon emitted when an electron goes from n = 3

Shapes and size of orbitals

s–orbitals: These orbitals are