Welcome to
Classification of Elements and
Periodicity in Properties
Why do we need to classify?
How do you find a book of your
interest in a library?
How difficult would it be if all the
books were mixed up?
We know that when books are
organised in the library, it is very easy
to identify the book but it may be a
tedious job when they are randomly
placed.
Why do we need to classify?
1…………….…………………………...………………………………………………118
….…………
Systematic way of organizing
knowledge by classifying elements.
Properties of elements repeat
themselves after regular intervals
Developments in Periodic Classification
Newlands’
Law of
Octaves
Mendeleev
Periodic
Table
Modern
Periodic
Table
Dobereiner’s
Triads
Dobereiner’s Law of Triads
Triads
Arrangement of the elements in increasing
order of their atomic mass
Group of three elements possessing
similar properties
Element Atomic Mass
K 39
Li 7
Na 23 7 + 39
2
= 23
Mean atomic mass
of 1st
& 3rd
element
Na
Li K
This rule seemed to work only
for a few elements. So, it was
dismissed.
Newlands’ Law of Octaves
Arrangement of the elements in increasing order of their atomic masses
Properties of every eighth element are similar to the first element
Sa Re Ga Ma Pa Dha Ni
Element Li Be B C N O F
Atomic
mass
7 9 11 12 14 16 19
Element Na Mg Al Si P S Cl
Atomic
mass
23 24 27 29 31 32 35.5
Element K Ca
Atomic
mass
39 40
Newlands’ Law of Octaves
Drawback of Newlands’ Octaves
Applicable
only upto
Ca
Mendeleev's Periodic Table
Elements with similar
properties occupy
same vertical column
Arranged 63 known
elements in increasing
order of atomic weight in a
tabular form
Periodic table
Vertical column
(8)
Group
Horizontal rows
(7)
Period
Mendeleev's Periodic Law
Physical and chemical properties of elements
are a periodic function of their atomic masses
Predicted some undiscovered elements and their properties
Eka-Aluminium (Gallium) & Eka-Silicon (Germanium)
Atomic mass of Be was corrected
Considering its valency 2 (2 × 4.5 = 9)
Drawbacks of Mendeleev’s Periodic Table
Hydrogen did not have a fixed position
No regular trend in increasing
order of atomic mass
Isotopes failed to comply with the periodic
table
Moseley’s Modification
Bombarded high speed electrons
on different metal surfaces
Plot of √𝜈 (frequency) v/s Z (atomic number)
gave a straight line
√𝜈 a (Z − b)
= a, b are
costants
Modern Periodic Law
Physical and chemical properties of elements
are a periodic function of their atomic number
Periodicity
Repetition of properties of elements after regular
intervals when elements are arranged in order of
increasing atomic number.
Periodic law is the consequence of the periodic
variation in electronic configuration.
Modern Periodic Table
Modern Periodic Table
Elements belonging to same period have same valence shell.
Periods Horizontal rows (7)
Elements of same group have similar valence shell electronic
configuration.
Group Vertical column (18)
Blocks of the Periodic Table
s-block
f-block
p-block
d-block
Based on
the type of
orbitals which
receives the
differentiating
electron
● H is placed outside the
periodic table though it has
last electron in s-orbital.
● He belongs to s-block but
placed in p-block with noble
gases.
Exceptions:
s-block
s-block
s-block
Last electron enters the
‘ns’ subshell
Outer electronic configuration
ns1-2
Groups 1-2 & all are metals
s-block
Group 1
Alkali metals
Group 2
Alkaline earth
metals
Outer electronic
configuration ns1
Outer electronic
configuration ns2
p-block
p-block
p-block
Last electron enters the
‘np’ subshell
Outer electronic configuration
ns2
np1-6
Groups 13-18 & includes
some metals, all nonmetals
and metalloids
p-block
13
14
15
16
Group
17
18
Boron family
Carbon family
Pnictogens
Chalcogens
Name
Halogens
Noble gases
d-block
d-block
d-block
Last electron enters the
(n - 1)d subshell
Outer electronic configuration
(n-1) d1-10
ns0-2
Groups are from 3 to 12 &
all are metals
d-block
3-d series
4-d series
Sc(Z = 21) - Zn(Z = 30)
Y(Z = 39) - Cd(Z = 48)
5-d series
6-d series
La(Z = 57) - Hg(Z = 80)
Ac(Z = 89) - Cn(Z = 112)
Transition series Elements
1st
2nd
3rd
4th
Forms a bridge between
s-block (chemically active) &
groups 13 & 14 (less active)
Transition elements
d-block
Zn, Cd and Hg are not transition elements
because they do not have partially filled
d-orbitals in neutral or in any stable
oxidation state
Classification of Elements and Periodicity in Properties chem.pdf
f-block
f-block
Last electron enters the
‘(n - 2)f’ subshell
Outer electronic configuration
(n-2) f1-14
(n-1) d0–1
ns2
Group 3 & all are metals
2nd
Inner
transition series
Actinides
Lanthanides
1st
Inner
transition series
Th(Z = 90) - Lr(Z = 103)
Ce(Z = 58) - Lu(Z = 71)
f-block
f-block
f-block
Elements after Uranium in the periodic table
are called Transuranic elements
Main group
elements
Elements of groups 1, 2 and 13–18
(except H)
Typical
elements
2nd
period elements except Ar
Remember!
Coinage
metals
Group 11 elements are Cu, Ag & Au
Remember!
Representative
elements
s-block elements along with
p-block elements
Transition
elements
Elements which have partially filled
d-orbitals in neutral state or in any stable
oxidation state
Inner transition
elements
Elements in which all the three shells i.e. n,
(n– 1) & (n – 2) shells are incomplete
Remember!
2
Atomic number of Noble Gases
10 18 36 54 86
He Ne Ar Kr Xe Rn
How are elements named in periodic table?
May be on
the name of
the scientist?
May be based
on the names of
planets, Greek
mythology…?
May be on
the place of
discovery?
May be on the
meaning of
elements with
its behavior?
How Elements Got their Names?
Name of
Elements
Place of
discovery
Behaviour
Planet names
Scientist
names
Americium
Hydrogen
Mercury
Bohrium
Roots are put together in order of digits from
0 to 9 which make the atomic number
“ium” is added at the end
Corresponding symbol has three letters
IUPAC Nomenclature for Elements Having Z > 100
Digit
0
Name
nil
1 un
9 enn
Abbreviation
n
u
e
2 bi
3 tri
b
t
4 quad
5 pent
q
p
6 hex
7 sept
h
s
8 oct o
IUPAC Nomenclature for Elements Having Z > 100
1 un
0 nil
5 pent
unp
Z = 105 unnilpentium
Subshell in which the
last electron enters is the block
Eg: 1s2
2s2
2p4
⇒ p - block
Write the electronic
configuration
Finding Position of an element in periodic table
Find block
s - block
Number of electrons in
the outer s-orbital is its
group number
p - block
(Number of electrons in
outermost shell) + 10
= group number
Find group
Finding Position of an element in periodic table
d - block
Number of electrons in
outermost shell +
penultimate d subshell
f - block Group 3
Find group
Finding Position of an element in periodic table
Z ≥ 103
Z = 100 + x ,
x = group number = 3
Example:
6
Z = 106
Group Number
Atomic number
Finding Position of an element in periodic table
Find group when Z ≥ 100
Highest value of
Principal Quantum Number
(n)
Write the electronic
configuration
Find period
Finding Position of an element in periodic table
On the
basis of
nature
Metals
Metalloids
Non Metals
Classification of elements
Metals Non-metals and Metalloids
Metals
Non - Metals
Metalloids
Classification of elements
Metal
Good conductor
Lose electron(s) easily
High lustre
Ductile & Malleable
Non-metal
Poor conductors
Gain electron(s) easily
Brittle
Classification of elements
Metalloids
Semiconductor
Properties depend
on conditions
Brittle
Classification of elements
Penetration
The proximity of
electrons in an
orbital to
the nucleus
s > p > d > f
Order of Penetration power
Consequence of
Penetration effect
Shielding
Effect
Comparison of Penetration Power
Measure of orbital’s closeness to the nucleus
r
𝚿
R
2
4𝜋r
2
3p
3s
3d
Shielding Effect
Outer electrons experience an attractive force from the
nucleus & repulsive forces from the other electrons
+3
Repulsion
Attraction
Shielding Effect
Attraction between the
outer electron & the
nucleus decreases
In a
multi-electron
system
Due to the
repulsions with the
inner electrons
Effect in which the inner electrons shield the valence
electron(s) from the attraction of the nucleus
s > p > d > f
Strength of Shielding effect
Effective Nuclear charge (Zeff
)
Shielding decreases the
nuclear attraction
Refers to the actual
charge experienced by
the outermost electrons
Z = Atomic number
𝛔 = Screening or Shielding constant
Zeff Z
= 𝛔
−
Effective Nuclear charge
Zeff
increases from left to right across a period
Li <
1.3
Be < B < C < N < O < F < Ne
1.95 2.60 3.25 3.90 4.55 5.20 5.85
For s block
elements
Zeff
increases slightly and becomes constant down a group
Li < Na ≃ K ≃ Rb ≃ Cs
1.3 2.2 2.2 2.2 2.2
Trends Across the Periodic Table
01 03
04
Electron gain
enthalpy
02
Electro-
negativity
05
Atomic
radius
Ionization
enthalpy
Electron
affinity
Atomic Radius
Distance between the centre of the nucleus and the
outermost electron(s) of an atom
Finding the size of an atom is
a lot more complicated
Size of an atom is very small
No sharp boundary exists
Atomic Radius
Size of an atom can be
measured using the internuclear
distance
between two identical atoms by
X-ray diffraction or other
spectroscopic techniques.
Atomic
radii
Covalent radii
Metallic radii
van der Waals
radii
Covalent radii
rcov
=
d
d
2
Generally used for non-metals
Units - picometer (pm) or Angstrom (Å)
Half the distance between the centres
of two nuclei of the same element
bonded by a single covalent bond
rA
dA-B = rB
+ 0.09
Δ
− 𝜒
● 𝜒 = Electronegativity (Pauling scale)
rA
=
dA-A
2
(in Å)
rB
=
dB-B
2
(in Å)
Schomaker & Stevenson equation
Covalent radii of Heteronuclear Diatomic Molecule
●
●
Metallic radii
d
rmetallic
=
d
2
Half the internuclear distance between two
adjacent metallic atoms in a crystalline lattice
structure
van der Waals Radii
van der
Waals radius
For Noble gas
For Non-metals
For Noble gases,
van der Waals Radii
Half the distance between the nuclei of two
non-bonded nearest neighbouring atoms of the
same element in its solid state
rvdw
d
Half the distance between the nuclei of two non-bonded
nearest neighbouring atoms of two adjacent molecules of
the same element in solid state
For Non-metals,
(
C
l
2
m
o
l
e
c
u
l
e
)
3
6
0
p
m
d
(Cl2
molecule) 99
pm
van der Waals Radii
rvdw
= 180 pm
rcovalent
= 99 pm
Comparison of Metallic and Covalent Radii
Metallic radius
rNa rCl
Covalent radius
van der
Waals radii
Metallic radii Covalent radii
Overlapping Radii
> >
Number of shells
Atomic Radius
Example
∝
Cs > Rb > K > Na > Li
Number of shells
Factors affecting Atomic radii
Atomic Radius
1
Effective nuclear charge
∝
Li > Be > B > C > N > O > F
Factors affecting Atomic radii
Effective nuclear charge
Example
Screening effect
Atomic Radius
Example
∝
Cs > Rb > K > Na > Li
Factors affecting Atomic radii
Screening effect
Atomic Radius
Example
∝
Factors affecting Atomic radii
N N N N N N
> >
1
Number of Bonds
Number of bonds
Variation of Atomic Radii in a Group
Atomic radius
Principal Quantum number (n)
Distance between valence electrons
& nucleus
Variation of Atomic Radii in a Group
300
250
200
150
100
50
Atomic number (Z)
Atomic
radius
(pm)
Li(152)
Na(186)
K(231)
Rb(244)
Cs(262)
F(72)
Cl(99)
Br(114)
I(133)
Alkali Metals
Halogens
Atomic Radius
Atomic number , Zeff
Attraction between valence electrons
& nucleus
Variation of Atomic Radii in a Period
Variation of Atomic Radii in a Period
2nd
Period
2 4 6 8 10
60
80
100
120
140
160
Atomic number (Z)
Atomic
radius
(pm)
Li
B
Be
N
F
C
O
Atomic radius increases (in a period from left to right)
Atomic Radii
Atomic radius
increases down
the group
Irregularities in Variation of Atomic radii
Generally van der Waals radius is larger
than the covalent & metallic radius
Atomic radius of an inert gas (18th
group)
is the largest in its period
Represented by van der Waals radius
(monatomic state)
Due to the poor shielding effect of d
electrons
Atomic Radius of Ga
Atomic Radius of Al >
Radii of the elements
decrease and then
become constant
1st
Transition series
Near the end,
radius increases
Atomic Radii trends in d block
Element Sc Ti V Cr Mn Fe Co Ni Cu Zn
Atomic radius (pm) 144 132 122 117 117 117 116 115 117 125
Sc - Cr
Cr - Cu
Cu - Zn
Zeff
dominates
Zeff
≃ Electronic repulsion
High electronic repulsion
4f subshell electrons exert very poor
shielding effect and cancel out the
normal size increase on moving down a
group
Lanthanoid Contraction
14 lanthanide elements
Lanthanum Hafnium
5d series
Exceptions in d-block elements
Due to
Lanthanoid contraction
Atomic radii of d block
elements : 3d < 4d ≅ 5d
But
Sc Y La
< <
4f electrons are absent in La
Covalent Radii of Transition Metals
1.8
1.7
1.6
1.5
1.4
1.3
1.2
1.1
4 (Ti)
5 (V) 6 (Cr) 7 (Mn) 8 (Fe) 9 (Co) 10 (Ni)
1
2
3
Group Number (1st
row element)
Covalent
Radius
(Å)
R
o
w
N
u
m
b
e
r
Ionic Radius
d
(Internuclear
distance)
rc ra
A
(Cation)
B
(Anion)
Ionic Radius
Cation
Smaller than its parent
atom
Less electrons than its
parent atom
More Zeff
e
p
electron
proton
< 1
Ionic Radius
Anion
Larger than its parent
atom
More electrons than its
parent atom
Less Zeff
e
p
electron
proton
> 1
Atom Cation Atom Anion
Ionic Radii (pm)
Li
152
Na
186
K
231
Rb
244
Cs
262
Li+
76
Na+
95
K+
138
Rb+
146
Cs+
174
F
72
Cl
99
Br
114
I
133
F-
136
Cl-
184
Br-
196
l-
216
Isoelectronic species
Atoms and ions which
contain the same
number of electrons
Zeff
For isoelectronic
species
Ionic radii
Al3+
Mg2+
Na+
F-
O2-
N3-
Ionic radii increases as Zeff
decreases
Li+
Mg2+
≈
>
For isotopes
Size of anion Size of atom Size of cation
> >
For same element
Remember !!!
35 37
rCl rCl
Smallest anion is F−
and not H−
Order of radii:
F−
< Cl−
< Br−
< H−
< I−
H−
: e/p ratio = 2
As e/p ratio is very high for H−
, its size is
abnormally bigger.
Did you know?
Ionization Energy
Minimum energy required to remove the most loosely bound
electron from an isolated gaseous atom in its ground state
M (g) M+
(g) + e-
Unit - kJ/mol, kcal/mol, eV
Ionization Energy
Quantitative measure of the tendency of an element to
lose an electron
Easier it is for a neutral
atom to change itself
to a positive ion
Smaller is the
ionization energy
Ionization energy for an atom is always positive
First Ionization Energy
Energy required to remove the outermost electron
from a gaseous neutral atom
M (g) M+
(g) + e-
, IE1
Second Ionization Energy
Energy required to remove the second most loosely
bound electron
M+
(g) M2+
(g) + e-
, IE2
Third Ionization Energy
Energy required to remove the third most loosely
bound electron
M2+
(g) M3+
(g) + e-
, IE3
I.E.1
< I.E.2
< I.E.3
...
Removal of an electron from
a cation is more difficult than
from a neutral gaseous atom
2nd
I.E. > 1st
I.E.
Therefore
Which is Larger - First, Second or Third I.E.?
Successive Ionization Energies
Element
Electronic
Configuration
I.E.1
(kJ/mol)
I.E.2
(kJ/mol)
I.E.3
(kJ/mol)
Li 1s2
2s1
520 7298 11815
Be 1s2
2s2
899 1757 14850
B 1s2
2s2
2p1
801 2427 3660
C 1s2
2s2
2p2
1086 2353 4620
N 1s2
2s2
2p3
1402 2856 4578
O 1s2
2s2
2p4
1314 3388 5300
F 1s2
2s2
2p5
1681 3374 6050
Ne 1s2
2s2
2p6
2080 3952 6122
I.E.
Factors affecting Ionization Energy
1 Size of an atom
2 Effective nuclear charge ( Zeff
) I.E.
3 Screening effect I.E.
4 Penetration Effect
I.E.
5 Electronic Configuration
Fully filled > Half filled > Partially filled
Order of I.E.
Ionization Energy in a Period
Across a period
Zeff
I.E.
Ionization Energy in a Group
Down the group
Size
I.E.
Ionization Energy
Ionization energy increases
Ionization
energy
increases
IE1
of the first 60 elements
10 20 30 40 50 60
500
1000
1500
2000
2500
Ne
He
Ar
Li Na
K
Kr
Rb
Xe
Cs
Atomic number (Z)
Δ
1
H
(kJ
/
mol)
Li B
< Be C O N F Ne
Order of First Ionization Energy
2nd
Period Element
< < < < < <
Zeff
in a period
Increases from
left to right
I.E.
Order of I.E. for 2nd
Period Elements
1st
I.E.
2nd
I.E.
Be C
< B N F O Ne Li
< < < < < <
Li B
< Be C O N F Ne
< < < < < <
For 13th
group
Order of First Ionization Energy
Lanthanoid Contraction
Poor shielding of d electron
In Al
< Ga Tl
< < < B
Points to Remember
I.E. of non-metals > I.E. of metals
Noble gases have the highest I.E. values
in any period
Caesium has the lowest I.E., hence it is used in
photoelectric cells
Helium has the highest I.E.
Metallic Character
Metallic character
I.E.
Metallic character means how
easily an element lose
electrons in chemical
reactions
Ionization
energy
increases
Metallic Character and Ionization Energy
Metallic
character
increases
Non-Metallic Character
Accept electrons
during chemical
reactions
Non-Metallic
Character
Non-Metallic character
I.E.
Metallic character decreases
Period 3
Group 5A
P
e
ri
o
d
s
Metallic
character
increases
Electron Gain Enthalpy (Δ H)
X (g) + e-
X-
(g) kJ/mol
Enthalpy change
when an electron is
added to a neutral
gaseous atom to
convert it into a
gaseous anion
eg
Electron Gain Enthalpy
Electron Gain Enthalpy
Positive Negative
When energy is
absorbed
When energy is
released
Factors affecting Electron Gain Enthalpy
Zeff
Half filled or fully
filled subshell
Atomic size
Magnitude of
electron gain
enthalpy
Δeg
H Screening effect
Electron Gain Enthalpy Across a Period
Across a period
Zeff
Magnitude of Δeg
H
Ne Be
< N
< Li
< B
< C
< O
< F
<
Trend in 2nd
Period
Fully filled subshell
Half filled subshell
Electron Gain Enthalpy Down the Group
Down the group
Size
Magnitude of Δeg
H
Electron Gain Enthalpy Down a Group
Cl > F S > O
P > N Si > C
Al > B
Magnitudes of Δeg
H of 3rd
period
elements are greater than
corresponding 2nd
period ‘p’ block
elements
It happens because 2nd
period elements (F and
O) have smallest size in
their respective group
and addition of extra
electron causes greater
repulsion as compared to
2nd
period elements.
Why Such Exceptions…?
Cl has the highest negative
Δeg
H value
It is easier to add an
electron to Cl and S due
to its larger size which
can accommodate extra
electron more easily
compared to 3rd
period
elements.
Δeg
H of noble gases is positive
because it already have stable
electronic configuration and after
addition of an electron, it becomes
comparatively unstable.
Magnitude of Electron Gain Enthalpy trends
Δeg
H increases
Δ
eg
H
increases
Successive Electron Gain Enthalpy
Δeg
H for the addition of a
second electron to a neutral
atom is positive
Electron repulsion outweighs
the nuclear attraction
O (g) + e−
→ O−
(g) ; Δeg
H1
= − 141 kJ/mol
O−
(g) + e−
→ O2−
(g) ; Δeg
H2
= + 744 kJ/mol
Second and subsequent electron gain
enthalpies are always positive.
Electron Affinity (E.A.)
Conventionally
defined as the energy
released when an
electron is added to the
valence shell of a
neutral isolated
gaseous atom
X (g) + e-
X-
(g) eV/atom, kJ/mol
Electron Affinity (E.A.)
Δeg
H = − E.A. − RT
5
2
● R : Universal Gas Constant
● T : Temperature (K)
Δeg
H = − E.A.
For comparison purpose in Periodic Trends,
we use both the terms interchangeably
At 0 K
Electron Affinity (E.A.)
Same as negative
Δeg
H
Order of E.A.
S Se
> Te
> Po
> O
>
Order of negative Δeg
H or E.A. in oxygen family
Remember !!!
The smallest value of I.E. of an element (Cs)
is even greater than the highest value of
E.A. of an element (Cl)
Electronegativity (E.N. or 𝜒)
Measure of the
tendency of an atom to
attract the shared
electrons towards itself in
a covalently bonded
molecule
E.N. is not a property of an isolated atom
Electronegativity
1
E.N. of an atom may be different
in different molecules
2
E.N. is not a measurable property
3
Electronegativity
Scales of E.N.
Pauling scale
Mulliken-Jaffe
scale
Allred-Rochow
scale
Pauling scale is the most commonly used scale for E.N.
Assigned
value 4.0
F
Highest
E.N.
Electronegativity
Electronegativity values (Pauling scale)
Factors Affecting Electronegativity
Distance between the nucleus & the
valence shell electrons
Force of attraction b/w the nucleus &
the valence shell electrons
Electronegativity value
Factors Affecting Electronegativity
Zeff
Electronegativity value
Force of attraction b/w the nucleus &
the valence shell electrons
Factors Affecting Electronegativity
Magnitude of positive charge
on the atom
Electronegativity value
Force of attraction b/w the nucleus & the
valence shell electrons
Electronegativity across a period
Li Be B C N O F
Elements
1.0 1.5 2.0 2.5 3.0 3.5 4.0
E.N. (Pauling Scale)
From left to right in a period,
Atomic radius , Electronegativity
Electronegativity down a group
F
Cl
Br
I
4.0
3.0
2.8
2.5
Elements
(Group 17)
Electronegativity value
Down the group
Atomic radius
Electronegativity
F has the highest electronegativity
1
Cs has the lowest electronegativity
2
3
4
Alkali metals have the lowest E.N.
in their respective period
Halogens have the highest E.N.
in their respective period
Some important points
Electronegativity
Strong tendency of non-metallic
elements to gain electrons
E.N. is directly related to the non-metallic
properties of elements
Cannot be measured
experimentally
Can be experimentally
measured
Electron Gain Enthalpy Electronegativity
Tendency of an atom in
a molecule to attract the
shared pair of electrons
Tendency of an isolated
gaseous atom to attract
an electron
Electron Gain Enthalpy vs Electronegativity
Electronegativity
Ionization Energy
Atomic Radius
Electron Affinity
Increases
Increases
Decreases
Increases
Decreases
Increases
Decreases
Decreases
Number of
electrons in the
outermost shell
Valence of
representative
elements
8 − (Number of
electrons in the
outermost shell)
OR
Valence
The term oxidation state is frequently
used for valence
Oxidation state of
an element in a
molecule or an ion
(Imaginary) charge the atom would have, if the
electron in each bond were located on the
more electronegative atom
Oxidation State (O.S.)
Na2
O
O.S. of Na
is + 1
O.S. of
O is -2
O is
more E.N.
than Na
Oxidation State (O.S.)
OF2
O.S. of
F is −1
O.S. of
O is +2
F is
more E.N.
than O
Oxidation State (O.S.)
What is Valency?
1
1
1
2
2
2
13
3
1,3
14
4
2,4
Group
No. of Valence
Electrons
Valency
15
5
3,5
16
6
2,4,6
17
7
1,3,5,7
18
8
0,8
Variation along a period
Number of valence electrons from left to right
increases from 1 to 8
Variation within a group
Down a group, the number of valence
electrons remains the same
All the elements in a group exhibit the
same valency
Valency and O.S.
Alkali Metal
Elements
Valency
of 1
Oxidation
State
of +1
Periodic Trends in Valency
1
LiH
2
CaH2
NaH
KH
Formula of
hydride
B2
H6
AlH3
Group 13
Li2
O
K2
O
Na2
O
Formula of
oxide
MgO
CaO
SrO
BaO
B2
O3
Al2
O3
Ga2
O3
In2
O3
Periodic Trends in Valency
14 15
Group 16
Formula of
hydride
NH3
PH3
AsH3
SbH3
H2
O
H2
S
H2
Se
H2
Te
CH4
SiH4
GeH4
SnH4
Formula of
oxide
N2
O3
, N2
O5
P4
O6
, P4
O10
As2
O3
, As2
O5
Sb2
O3
, Sb2
O5
CO2
SiO2
GeO2
SnO2
Bi2
O3
PbO2
SO3
SeO3
TeO3
Periodic Trends and Chemical Reactivity
Δeg
H increases from left to right
in a period
I.E. increase from left to right
in a period
High chemical reactivity at
the two extremes( left side due to
less I.E. and right side due to high
electron affinity)
Acidic oxides
Oxides of non-metals
React with bases
Basic oxides
Oxides of metals
React with acids
Oxides
Oxides
Amphoteric oxides
Reacts with acids as well
as bases
BeO, Al2
O3
, ZnO, Cr2
O3
Neutral oxides
Does not react with an
acid or a base
CO, N2
O, NO
Oxides
Oxide formed by the element on the extreme
left is the most basic (Na2
O)
Oxide formed by the element on the extreme
right is the most acidic (Cl2
O7
)
Anomalous
behaviour
Absence of
d orbitals
(Maximum
covalency = 4)
Small size
& high
charge/radius
ratio in their
respective
groups
Highest
electronegativity
in their respective
groups
Why Anomalous behaviour for 2nd
period elements?
Diagonal Relationship
Li & Be show exceptional behaviour
from other elements of their respective
groups
Form compounds with pronounced
covalent character
Other members of their groups
predominantly form ionic compounds
Li & Be are more similar to second
element of their following group,
i.e., Mg & Al respectively. This is
called diagonal relationship in
periodic properties.

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Classification of Elements and Periodicity in Properties chem.pdf

  • 1. Welcome to Classification of Elements and Periodicity in Properties
  • 2. Why do we need to classify? How do you find a book of your interest in a library? How difficult would it be if all the books were mixed up? We know that when books are organised in the library, it is very easy to identify the book but it may be a tedious job when they are randomly placed.
  • 3. Why do we need to classify? 1…………….…………………………...………………………………………………118 ….………… Systematic way of organizing knowledge by classifying elements. Properties of elements repeat themselves after regular intervals
  • 4. Developments in Periodic Classification Newlands’ Law of Octaves Mendeleev Periodic Table Modern Periodic Table Dobereiner’s Triads
  • 5. Dobereiner’s Law of Triads Triads Arrangement of the elements in increasing order of their atomic mass Group of three elements possessing similar properties Element Atomic Mass K 39 Li 7 Na 23 7 + 39 2 = 23 Mean atomic mass of 1st & 3rd element Na Li K This rule seemed to work only for a few elements. So, it was dismissed.
  • 6. Newlands’ Law of Octaves Arrangement of the elements in increasing order of their atomic masses Properties of every eighth element are similar to the first element
  • 7. Sa Re Ga Ma Pa Dha Ni Element Li Be B C N O F Atomic mass 7 9 11 12 14 16 19 Element Na Mg Al Si P S Cl Atomic mass 23 24 27 29 31 32 35.5 Element K Ca Atomic mass 39 40 Newlands’ Law of Octaves Drawback of Newlands’ Octaves Applicable only upto Ca
  • 8. Mendeleev's Periodic Table Elements with similar properties occupy same vertical column Arranged 63 known elements in increasing order of atomic weight in a tabular form Periodic table Vertical column (8) Group Horizontal rows (7) Period
  • 9. Mendeleev's Periodic Law Physical and chemical properties of elements are a periodic function of their atomic masses Predicted some undiscovered elements and their properties Eka-Aluminium (Gallium) & Eka-Silicon (Germanium) Atomic mass of Be was corrected Considering its valency 2 (2 × 4.5 = 9)
  • 10. Drawbacks of Mendeleev’s Periodic Table Hydrogen did not have a fixed position No regular trend in increasing order of atomic mass Isotopes failed to comply with the periodic table
  • 11. Moseley’s Modification Bombarded high speed electrons on different metal surfaces Plot of √𝜈 (frequency) v/s Z (atomic number) gave a straight line √𝜈 a (Z − b) = a, b are costants
  • 12. Modern Periodic Law Physical and chemical properties of elements are a periodic function of their atomic number
  • 13. Periodicity Repetition of properties of elements after regular intervals when elements are arranged in order of increasing atomic number. Periodic law is the consequence of the periodic variation in electronic configuration.
  • 15. Modern Periodic Table Elements belonging to same period have same valence shell. Periods Horizontal rows (7) Elements of same group have similar valence shell electronic configuration. Group Vertical column (18)
  • 16. Blocks of the Periodic Table s-block f-block p-block d-block Based on the type of orbitals which receives the differentiating electron ● H is placed outside the periodic table though it has last electron in s-orbital. ● He belongs to s-block but placed in p-block with noble gases. Exceptions:
  • 18. s-block s-block Last electron enters the ‘ns’ subshell Outer electronic configuration ns1-2 Groups 1-2 & all are metals
  • 19. s-block Group 1 Alkali metals Group 2 Alkaline earth metals Outer electronic configuration ns1 Outer electronic configuration ns2
  • 21. p-block p-block Last electron enters the ‘np’ subshell Outer electronic configuration ns2 np1-6 Groups 13-18 & includes some metals, all nonmetals and metalloids
  • 24. d-block d-block Last electron enters the (n - 1)d subshell Outer electronic configuration (n-1) d1-10 ns0-2 Groups are from 3 to 12 & all are metals
  • 25. d-block 3-d series 4-d series Sc(Z = 21) - Zn(Z = 30) Y(Z = 39) - Cd(Z = 48) 5-d series 6-d series La(Z = 57) - Hg(Z = 80) Ac(Z = 89) - Cn(Z = 112) Transition series Elements 1st 2nd 3rd 4th Forms a bridge between s-block (chemically active) & groups 13 & 14 (less active) Transition elements
  • 26. d-block Zn, Cd and Hg are not transition elements because they do not have partially filled d-orbitals in neutral or in any stable oxidation state
  • 28. f-block f-block Last electron enters the ‘(n - 2)f’ subshell Outer electronic configuration (n-2) f1-14 (n-1) d0–1 ns2 Group 3 & all are metals
  • 29. 2nd Inner transition series Actinides Lanthanides 1st Inner transition series Th(Z = 90) - Lr(Z = 103) Ce(Z = 58) - Lu(Z = 71) f-block f-block
  • 30. f-block Elements after Uranium in the periodic table are called Transuranic elements
  • 31. Main group elements Elements of groups 1, 2 and 13–18 (except H) Typical elements 2nd period elements except Ar Remember! Coinage metals Group 11 elements are Cu, Ag & Au
  • 32. Remember! Representative elements s-block elements along with p-block elements Transition elements Elements which have partially filled d-orbitals in neutral state or in any stable oxidation state Inner transition elements Elements in which all the three shells i.e. n, (n– 1) & (n – 2) shells are incomplete
  • 33. Remember! 2 Atomic number of Noble Gases 10 18 36 54 86 He Ne Ar Kr Xe Rn
  • 34. How are elements named in periodic table? May be on the name of the scientist? May be based on the names of planets, Greek mythology…? May be on the place of discovery? May be on the meaning of elements with its behavior?
  • 35. How Elements Got their Names? Name of Elements Place of discovery Behaviour Planet names Scientist names Americium Hydrogen Mercury Bohrium
  • 36. Roots are put together in order of digits from 0 to 9 which make the atomic number “ium” is added at the end Corresponding symbol has three letters IUPAC Nomenclature for Elements Having Z > 100
  • 37. Digit 0 Name nil 1 un 9 enn Abbreviation n u e 2 bi 3 tri b t 4 quad 5 pent q p 6 hex 7 sept h s 8 oct o IUPAC Nomenclature for Elements Having Z > 100 1 un 0 nil 5 pent unp Z = 105 unnilpentium
  • 38. Subshell in which the last electron enters is the block Eg: 1s2 2s2 2p4 ⇒ p - block Write the electronic configuration Finding Position of an element in periodic table Find block
  • 39. s - block Number of electrons in the outer s-orbital is its group number p - block (Number of electrons in outermost shell) + 10 = group number Find group Finding Position of an element in periodic table
  • 40. d - block Number of electrons in outermost shell + penultimate d subshell f - block Group 3 Find group Finding Position of an element in periodic table
  • 41. Z ≥ 103 Z = 100 + x , x = group number = 3 Example: 6 Z = 106 Group Number Atomic number Finding Position of an element in periodic table Find group when Z ≥ 100
  • 42. Highest value of Principal Quantum Number (n) Write the electronic configuration Find period Finding Position of an element in periodic table
  • 43. On the basis of nature Metals Metalloids Non Metals Classification of elements
  • 44. Metals Non-metals and Metalloids Metals Non - Metals Metalloids
  • 45. Classification of elements Metal Good conductor Lose electron(s) easily High lustre Ductile & Malleable
  • 46. Non-metal Poor conductors Gain electron(s) easily Brittle Classification of elements
  • 48. Penetration The proximity of electrons in an orbital to the nucleus s > p > d > f Order of Penetration power Consequence of Penetration effect Shielding Effect
  • 49. Comparison of Penetration Power Measure of orbital’s closeness to the nucleus r 𝚿 R 2 4𝜋r 2 3p 3s 3d
  • 50. Shielding Effect Outer electrons experience an attractive force from the nucleus & repulsive forces from the other electrons +3 Repulsion Attraction
  • 51. Shielding Effect Attraction between the outer electron & the nucleus decreases In a multi-electron system Due to the repulsions with the inner electrons Effect in which the inner electrons shield the valence electron(s) from the attraction of the nucleus s > p > d > f Strength of Shielding effect
  • 52. Effective Nuclear charge (Zeff ) Shielding decreases the nuclear attraction Refers to the actual charge experienced by the outermost electrons Z = Atomic number 𝛔 = Screening or Shielding constant Zeff Z = 𝛔 −
  • 53. Effective Nuclear charge Zeff increases from left to right across a period Li < 1.3 Be < B < C < N < O < F < Ne 1.95 2.60 3.25 3.90 4.55 5.20 5.85 For s block elements Zeff increases slightly and becomes constant down a group Li < Na ≃ K ≃ Rb ≃ Cs 1.3 2.2 2.2 2.2 2.2
  • 54. Trends Across the Periodic Table 01 03 04 Electron gain enthalpy 02 Electro- negativity 05 Atomic radius Ionization enthalpy Electron affinity
  • 55. Atomic Radius Distance between the centre of the nucleus and the outermost electron(s) of an atom Finding the size of an atom is a lot more complicated Size of an atom is very small No sharp boundary exists
  • 56. Atomic Radius Size of an atom can be measured using the internuclear distance between two identical atoms by X-ray diffraction or other spectroscopic techniques. Atomic radii Covalent radii Metallic radii van der Waals radii
  • 57. Covalent radii rcov = d d 2 Generally used for non-metals Units - picometer (pm) or Angstrom (Å) Half the distance between the centres of two nuclei of the same element bonded by a single covalent bond
  • 58. rA dA-B = rB + 0.09 Δ − 𝜒 ● 𝜒 = Electronegativity (Pauling scale) rA = dA-A 2 (in Å) rB = dB-B 2 (in Å) Schomaker & Stevenson equation Covalent radii of Heteronuclear Diatomic Molecule ● ●
  • 59. Metallic radii d rmetallic = d 2 Half the internuclear distance between two adjacent metallic atoms in a crystalline lattice structure
  • 60. van der Waals Radii van der Waals radius For Noble gas For Non-metals
  • 61. For Noble gases, van der Waals Radii Half the distance between the nuclei of two non-bonded nearest neighbouring atoms of the same element in its solid state rvdw d
  • 62. Half the distance between the nuclei of two non-bonded nearest neighbouring atoms of two adjacent molecules of the same element in solid state For Non-metals, ( C l 2 m o l e c u l e ) 3 6 0 p m d (Cl2 molecule) 99 pm van der Waals Radii rvdw = 180 pm rcovalent = 99 pm
  • 63. Comparison of Metallic and Covalent Radii Metallic radius rNa rCl Covalent radius van der Waals radii Metallic radii Covalent radii Overlapping Radii > >
  • 64. Number of shells Atomic Radius Example ∝ Cs > Rb > K > Na > Li Number of shells Factors affecting Atomic radii
  • 65. Atomic Radius 1 Effective nuclear charge ∝ Li > Be > B > C > N > O > F Factors affecting Atomic radii Effective nuclear charge Example
  • 66. Screening effect Atomic Radius Example ∝ Cs > Rb > K > Na > Li Factors affecting Atomic radii Screening effect
  • 67. Atomic Radius Example ∝ Factors affecting Atomic radii N N N N N N > > 1 Number of Bonds Number of bonds
  • 68. Variation of Atomic Radii in a Group Atomic radius Principal Quantum number (n) Distance between valence electrons & nucleus
  • 69. Variation of Atomic Radii in a Group 300 250 200 150 100 50 Atomic number (Z) Atomic radius (pm) Li(152) Na(186) K(231) Rb(244) Cs(262) F(72) Cl(99) Br(114) I(133) Alkali Metals Halogens
  • 70. Atomic Radius Atomic number , Zeff Attraction between valence electrons & nucleus Variation of Atomic Radii in a Period
  • 71. Variation of Atomic Radii in a Period 2nd Period 2 4 6 8 10 60 80 100 120 140 160 Atomic number (Z) Atomic radius (pm) Li B Be N F C O
  • 72. Atomic radius increases (in a period from left to right) Atomic Radii Atomic radius increases down the group
  • 73. Irregularities in Variation of Atomic radii Generally van der Waals radius is larger than the covalent & metallic radius Atomic radius of an inert gas (18th group) is the largest in its period Represented by van der Waals radius (monatomic state) Due to the poor shielding effect of d electrons Atomic Radius of Ga Atomic Radius of Al >
  • 74. Radii of the elements decrease and then become constant 1st Transition series Near the end, radius increases Atomic Radii trends in d block Element Sc Ti V Cr Mn Fe Co Ni Cu Zn Atomic radius (pm) 144 132 122 117 117 117 116 115 117 125 Sc - Cr Cr - Cu Cu - Zn Zeff dominates Zeff ≃ Electronic repulsion High electronic repulsion
  • 75. 4f subshell electrons exert very poor shielding effect and cancel out the normal size increase on moving down a group Lanthanoid Contraction 14 lanthanide elements Lanthanum Hafnium 5d series
  • 76. Exceptions in d-block elements Due to Lanthanoid contraction Atomic radii of d block elements : 3d < 4d ≅ 5d But Sc Y La < < 4f electrons are absent in La
  • 77. Covalent Radii of Transition Metals 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 4 (Ti) 5 (V) 6 (Cr) 7 (Mn) 8 (Fe) 9 (Co) 10 (Ni) 1 2 3 Group Number (1st row element) Covalent Radius (Å) R o w N u m b e r
  • 79. Ionic Radius Cation Smaller than its parent atom Less electrons than its parent atom More Zeff e p electron proton < 1
  • 80. Ionic Radius Anion Larger than its parent atom More electrons than its parent atom Less Zeff e p electron proton > 1
  • 81. Atom Cation Atom Anion Ionic Radii (pm) Li 152 Na 186 K 231 Rb 244 Cs 262 Li+ 76 Na+ 95 K+ 138 Rb+ 146 Cs+ 174 F 72 Cl 99 Br 114 I 133 F- 136 Cl- 184 Br- 196 l- 216
  • 82. Isoelectronic species Atoms and ions which contain the same number of electrons Zeff For isoelectronic species Ionic radii Al3+ Mg2+ Na+ F- O2- N3- Ionic radii increases as Zeff decreases
  • 83. Li+ Mg2+ ≈ > For isotopes Size of anion Size of atom Size of cation > > For same element Remember !!! 35 37 rCl rCl
  • 84. Smallest anion is F− and not H− Order of radii: F− < Cl− < Br− < H− < I− H− : e/p ratio = 2 As e/p ratio is very high for H− , its size is abnormally bigger. Did you know?
  • 85. Ionization Energy Minimum energy required to remove the most loosely bound electron from an isolated gaseous atom in its ground state M (g) M+ (g) + e- Unit - kJ/mol, kcal/mol, eV
  • 86. Ionization Energy Quantitative measure of the tendency of an element to lose an electron Easier it is for a neutral atom to change itself to a positive ion Smaller is the ionization energy Ionization energy for an atom is always positive
  • 87. First Ionization Energy Energy required to remove the outermost electron from a gaseous neutral atom M (g) M+ (g) + e- , IE1
  • 88. Second Ionization Energy Energy required to remove the second most loosely bound electron M+ (g) M2+ (g) + e- , IE2
  • 89. Third Ionization Energy Energy required to remove the third most loosely bound electron M2+ (g) M3+ (g) + e- , IE3
  • 90. I.E.1 < I.E.2 < I.E.3 ... Removal of an electron from a cation is more difficult than from a neutral gaseous atom 2nd I.E. > 1st I.E. Therefore Which is Larger - First, Second or Third I.E.?
  • 91. Successive Ionization Energies Element Electronic Configuration I.E.1 (kJ/mol) I.E.2 (kJ/mol) I.E.3 (kJ/mol) Li 1s2 2s1 520 7298 11815 Be 1s2 2s2 899 1757 14850 B 1s2 2s2 2p1 801 2427 3660 C 1s2 2s2 2p2 1086 2353 4620 N 1s2 2s2 2p3 1402 2856 4578 O 1s2 2s2 2p4 1314 3388 5300 F 1s2 2s2 2p5 1681 3374 6050 Ne 1s2 2s2 2p6 2080 3952 6122
  • 92. I.E. Factors affecting Ionization Energy 1 Size of an atom 2 Effective nuclear charge ( Zeff ) I.E. 3 Screening effect I.E. 4 Penetration Effect I.E. 5 Electronic Configuration Fully filled > Half filled > Partially filled Order of I.E.
  • 93. Ionization Energy in a Period Across a period Zeff I.E.
  • 94. Ionization Energy in a Group Down the group Size I.E.
  • 95. Ionization Energy Ionization energy increases Ionization energy increases
  • 96. IE1 of the first 60 elements 10 20 30 40 50 60 500 1000 1500 2000 2500 Ne He Ar Li Na K Kr Rb Xe Cs Atomic number (Z) Δ 1 H (kJ / mol)
  • 97. Li B < Be C O N F Ne Order of First Ionization Energy 2nd Period Element < < < < < < Zeff in a period Increases from left to right I.E.
  • 98. Order of I.E. for 2nd Period Elements 1st I.E. 2nd I.E. Be C < B N F O Ne Li < < < < < < Li B < Be C O N F Ne < < < < < <
  • 99. For 13th group Order of First Ionization Energy Lanthanoid Contraction Poor shielding of d electron In Al < Ga Tl < < < B
  • 100. Points to Remember I.E. of non-metals > I.E. of metals Noble gases have the highest I.E. values in any period Caesium has the lowest I.E., hence it is used in photoelectric cells Helium has the highest I.E.
  • 101. Metallic Character Metallic character I.E. Metallic character means how easily an element lose electrons in chemical reactions
  • 102. Ionization energy increases Metallic Character and Ionization Energy Metallic character increases
  • 103. Non-Metallic Character Accept electrons during chemical reactions Non-Metallic Character Non-Metallic character I.E.
  • 104. Metallic character decreases Period 3 Group 5A P e ri o d s Metallic character increases
  • 105. Electron Gain Enthalpy (Δ H) X (g) + e- X- (g) kJ/mol Enthalpy change when an electron is added to a neutral gaseous atom to convert it into a gaseous anion eg
  • 106. Electron Gain Enthalpy Electron Gain Enthalpy Positive Negative When energy is absorbed When energy is released
  • 107. Factors affecting Electron Gain Enthalpy Zeff Half filled or fully filled subshell Atomic size Magnitude of electron gain enthalpy Δeg H Screening effect
  • 108. Electron Gain Enthalpy Across a Period Across a period Zeff Magnitude of Δeg H
  • 109. Ne Be < N < Li < B < C < O < F < Trend in 2nd Period Fully filled subshell Half filled subshell
  • 110. Electron Gain Enthalpy Down the Group Down the group Size Magnitude of Δeg H
  • 111. Electron Gain Enthalpy Down a Group Cl > F S > O P > N Si > C Al > B Magnitudes of Δeg H of 3rd period elements are greater than corresponding 2nd period ‘p’ block elements It happens because 2nd period elements (F and O) have smallest size in their respective group and addition of extra electron causes greater repulsion as compared to 2nd period elements.
  • 112. Why Such Exceptions…? Cl has the highest negative Δeg H value It is easier to add an electron to Cl and S due to its larger size which can accommodate extra electron more easily compared to 3rd period elements. Δeg H of noble gases is positive because it already have stable electronic configuration and after addition of an electron, it becomes comparatively unstable.
  • 113. Magnitude of Electron Gain Enthalpy trends Δeg H increases Δ eg H increases
  • 114. Successive Electron Gain Enthalpy Δeg H for the addition of a second electron to a neutral atom is positive Electron repulsion outweighs the nuclear attraction O (g) + e− → O− (g) ; Δeg H1 = − 141 kJ/mol O− (g) + e− → O2− (g) ; Δeg H2 = + 744 kJ/mol Second and subsequent electron gain enthalpies are always positive.
  • 115. Electron Affinity (E.A.) Conventionally defined as the energy released when an electron is added to the valence shell of a neutral isolated gaseous atom X (g) + e- X- (g) eV/atom, kJ/mol
  • 116. Electron Affinity (E.A.) Δeg H = − E.A. − RT 5 2 ● R : Universal Gas Constant ● T : Temperature (K) Δeg H = − E.A. For comparison purpose in Periodic Trends, we use both the terms interchangeably At 0 K
  • 117. Electron Affinity (E.A.) Same as negative Δeg H Order of E.A. S Se > Te > Po > O > Order of negative Δeg H or E.A. in oxygen family
  • 118. Remember !!! The smallest value of I.E. of an element (Cs) is even greater than the highest value of E.A. of an element (Cl)
  • 119. Electronegativity (E.N. or 𝜒) Measure of the tendency of an atom to attract the shared electrons towards itself in a covalently bonded molecule
  • 120. E.N. is not a property of an isolated atom Electronegativity 1 E.N. of an atom may be different in different molecules 2 E.N. is not a measurable property 3
  • 121. Electronegativity Scales of E.N. Pauling scale Mulliken-Jaffe scale Allred-Rochow scale
  • 122. Pauling scale is the most commonly used scale for E.N. Assigned value 4.0 F Highest E.N. Electronegativity
  • 124. Factors Affecting Electronegativity Distance between the nucleus & the valence shell electrons Force of attraction b/w the nucleus & the valence shell electrons Electronegativity value
  • 125. Factors Affecting Electronegativity Zeff Electronegativity value Force of attraction b/w the nucleus & the valence shell electrons
  • 126. Factors Affecting Electronegativity Magnitude of positive charge on the atom Electronegativity value Force of attraction b/w the nucleus & the valence shell electrons
  • 127. Electronegativity across a period Li Be B C N O F Elements 1.0 1.5 2.0 2.5 3.0 3.5 4.0 E.N. (Pauling Scale) From left to right in a period, Atomic radius , Electronegativity
  • 128. Electronegativity down a group F Cl Br I 4.0 3.0 2.8 2.5 Elements (Group 17) Electronegativity value Down the group Atomic radius Electronegativity
  • 129. F has the highest electronegativity 1 Cs has the lowest electronegativity 2 3 4 Alkali metals have the lowest E.N. in their respective period Halogens have the highest E.N. in their respective period Some important points
  • 130. Electronegativity Strong tendency of non-metallic elements to gain electrons E.N. is directly related to the non-metallic properties of elements
  • 131. Cannot be measured experimentally Can be experimentally measured Electron Gain Enthalpy Electronegativity Tendency of an atom in a molecule to attract the shared pair of electrons Tendency of an isolated gaseous atom to attract an electron Electron Gain Enthalpy vs Electronegativity
  • 132. Electronegativity Ionization Energy Atomic Radius Electron Affinity Increases Increases Decreases Increases Decreases Increases Decreases Decreases
  • 133. Number of electrons in the outermost shell Valence of representative elements 8 − (Number of electrons in the outermost shell) OR Valence
  • 134. The term oxidation state is frequently used for valence Oxidation state of an element in a molecule or an ion (Imaginary) charge the atom would have, if the electron in each bond were located on the more electronegative atom Oxidation State (O.S.)
  • 135. Na2 O O.S. of Na is + 1 O.S. of O is -2 O is more E.N. than Na Oxidation State (O.S.)
  • 136. OF2 O.S. of F is −1 O.S. of O is +2 F is more E.N. than O Oxidation State (O.S.)
  • 137. What is Valency? 1 1 1 2 2 2 13 3 1,3 14 4 2,4 Group No. of Valence Electrons Valency 15 5 3,5 16 6 2,4,6 17 7 1,3,5,7 18 8 0,8
  • 138. Variation along a period Number of valence electrons from left to right increases from 1 to 8
  • 139. Variation within a group Down a group, the number of valence electrons remains the same All the elements in a group exhibit the same valency
  • 140. Valency and O.S. Alkali Metal Elements Valency of 1 Oxidation State of +1
  • 141. Periodic Trends in Valency 1 LiH 2 CaH2 NaH KH Formula of hydride B2 H6 AlH3 Group 13 Li2 O K2 O Na2 O Formula of oxide MgO CaO SrO BaO B2 O3 Al2 O3 Ga2 O3 In2 O3
  • 142. Periodic Trends in Valency 14 15 Group 16 Formula of hydride NH3 PH3 AsH3 SbH3 H2 O H2 S H2 Se H2 Te CH4 SiH4 GeH4 SnH4 Formula of oxide N2 O3 , N2 O5 P4 O6 , P4 O10 As2 O3 , As2 O5 Sb2 O3 , Sb2 O5 CO2 SiO2 GeO2 SnO2 Bi2 O3 PbO2 SO3 SeO3 TeO3
  • 143. Periodic Trends and Chemical Reactivity Δeg H increases from left to right in a period I.E. increase from left to right in a period High chemical reactivity at the two extremes( left side due to less I.E. and right side due to high electron affinity)
  • 144. Acidic oxides Oxides of non-metals React with bases Basic oxides Oxides of metals React with acids Oxides
  • 145. Oxides Amphoteric oxides Reacts with acids as well as bases BeO, Al2 O3 , ZnO, Cr2 O3 Neutral oxides Does not react with an acid or a base CO, N2 O, NO
  • 146. Oxides Oxide formed by the element on the extreme left is the most basic (Na2 O) Oxide formed by the element on the extreme right is the most acidic (Cl2 O7 )
  • 147. Anomalous behaviour Absence of d orbitals (Maximum covalency = 4) Small size & high charge/radius ratio in their respective groups Highest electronegativity in their respective groups Why Anomalous behaviour for 2nd period elements?
  • 148. Diagonal Relationship Li & Be show exceptional behaviour from other elements of their respective groups Form compounds with pronounced covalent character Other members of their groups predominantly form ionic compounds Li & Be are more similar to second element of their following group, i.e., Mg & Al respectively. This is called diagonal relationship in periodic properties.