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For JEE (main & Advanced)
FOURTH EDITION
Visit us at https://www.wileyindia.com/resources/
J.D. Lee
Concise
Inorganic Chemistry
for JEE (Main & Advanced)
@iitjeehelps
@iitjeehelps
J.D. Lee
Concise
Inorganic Chemistry
for JEE (Main & Advanced)
Adapted by
Sudarsan Guha
@iitjeehelps
J.D. Lee
Concise
Inorganic Chemistry
for JEE (Main & Advanced)
Copyright © 2019 by Wiley India Pvt. Ltd., 4436/7, Ansari Road, Daryaganj, New Delhi-110002.
All rights reserved. No part of this book may be reproduced, stored in a retrieval system, or transmitted in any form or by any
means, electronic, mechanical, photocopying, recording or scanning without the written permission of the publisher. This
book is an adaptation of Concise Inorganic Chemistry 5/e by J.D. Lee (ISBN: 978-81-265-1554-7). All rights remain with
respective holders.
Limits of Liability: While the publisher and the author have used their best efforts in preparing this book, Wiley and the
author make no representation or warranties with respect to the accuracy or completeness of the contents of this book, and
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Preface
Concise Inorganic Chemistry by J.D. Lee is a book widely used by students reparing for
JEE as the most comprehensive and authentic text for understanding Inorganic Chemistry.
The purpose of adaptation of this book is to provide a complete textbook of Inorganic
Chemistry that covers the entire syllabus of JEE (Main and Advanced)in proper sequence
of topics and provides in-depth explanation of topics. The use of book should give confidence
to the students to apply their knowledge to problem-solving and attempting JEE.
In this new (fourth) edition, major changes have been made in the Chapter 8: Hydrogen,
where the concept of hydrogen bonding is now explained with specific examples relevant
to JEE. Chapter 9: The s-Block Elements has been made more concise with more focus on
topics required from JEE perspective. Major changes have been made in Chapter 10: The
p-Block Elements. It is now divided into six separate parts as Group 13, Group 14, Group
15, Group 16, Group 17 and Group 18 Elements. Each part is followed by a separate set
of exercises for that particular group. Miscellaneous questions based on multiple concepts
have been placed at the end of the chapter. Apart from this new questions have been
included in the exercises at the end of most of the chapters.
For the future also, any suggestions for the improvement of this book are welcome by
the author.
Sudarsan Guha
M. Tech. (IIT-Kanpur)
@iitjeehelps
@iitjeehelps
Concise Inorganic Chemistry by J.D. Lee has been the definitive text for learning
Inorganic Chemistry since its first edition appeared about 45 years ago. The book captures
the fundamentals of the subject in a simple and logical framework of factual knowledge.
The description is long enough to cover the essentials, yet short enough to be interesting. Its
unparalleled approach to teaching Inorganic Chemistry is the reason why it is probably the
most favoured resource for an IIT aspirant like you today.
In collaboration with experts in JEE (Main & Advanced) coaching, the fifth edition of
the original book has now been adapted to give you the best book available in Inorganic
Chemistry for preparing for the toughest engineering entrance exam in India. This adaptation
offers the dual advantage of unmatched explanation of concepts as developed by “Master
teacher” and appropriate applications of the concepts to problem solving as developed by
an expert in this area.
Let’s walk through some of the special book features that will help you in your efforts
to take the JEE (Main & Advanced) with confidence.
CHAPTER OPENER
Each chapter starts with an
opening vignette related to the
topic, and listing of contents of
that chapter. This gives you an
overview of the chapter and
helps to identify the extent of
coverage.
CONCEPT EXPLANATION
Concepts are explained in a man-
ner easy to read and understand.
They are descriptive to the extent
required and provide reasons for
the structure, properties and reac-
tions of compounds. Many fasci-
nating applications of inorganic
compounds are also explained.
@iitjeehelps
FIGURES
The text is sprinkled with
multiple figures which pre-
sent two-dimensional rep-
resentation of compounds
and their structures. This
visual representation en-
hances understanding and
helps the student visualize
what a molecule may look
like.
TABLES
A large number of tables
capture data on structure,
properties and other such
parameters. The tabular repre-
sentation supports compara-
tive study of properties and
draws out changing trends in
them. The trends of various
properties of elements along
the periodic table are also
amply illustrated.
Application of concepts to problem solving is the core of JEE (Main & Advanced),
so it is important to test our understanding of concepts. For the test to be effective,
the assessment technique should be comprehensive and in the context of this
book, also in resonance with the JEE Main and JEE Advanced paper pattern.
Each part of the assessment should be modeled on the actual paper pattern
because unless the student practices the JEE way, he/she will not be sufficiently
equipped to take the examination. Keeping this in mind, the assessment has been
divided into:
@iitjeehelps
SINGLE CORRECT CHOICE TYPE QUESTIONS
These are the regular mul-
tiple choice questions with
four choices provided. Only
one among the four choices
will be the correct answer.
SI units for energy are used throughout this edition, thus making a comparison of thermo-
dynamic properties easier. Ionization energies are quoted in kJ mol–1, rather than ionization
potentials in eV. Older data from other sources use eV and may be converted into SI units
(1 kcal = 4.184 kJ, and 1 eV = 23.06 × 4.184 kJ mol–1).
Meters are strictly the SI units for distance, and bond lengths are sometimes quoted in
nanometers (1 mm = 10–9 m). However Ångström units Å (10–10 m) are a permitted unit of
length, and are widely used by crystallographers because they give a convenient range of
numbers for bond lengths. Most bonds are between 1 and 2 Å (0.1 to 0.2 nm). Ångström
units are used throughout for bond lengths.
The positions of absorption peaks in spectra are quoted in wave numbers cm–1, because
instruments are calibrated in these units. It must be remembered that these are not SI units,
and should be multiplied by 100 to give SI units of m–1, or multiplied by 11.96 to give J mol–1.
The SI units of density are kg m–3, making the density of water 1000 kg m–3. This conven-
tion is not widely accepted, so the older units of g cm–3 are retained so water has a density
of 1 g cm–3.
In the section on magnetism both SI units and Debye units are given, and the relation
between the two is explained. For inorganic chemists who simply want to find the number
of unpaired electron spins in a transition metal ion, Debye units are much more convenient.
I II III IV V VI VII 0
IA IIA IIIB IVB VB VIB VIIB <…VIIIB…> IB IIB IIIA IVA VA VIA VIIA VIIIA
H He
Li Be B C N O F Ne
Na Mg Al Si P S Cl Ar
K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr
Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe
Cs Ba La Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
F. APPENDICES
Contents
Prefacev
Note to the Student vii
1. Structure of an Atom 1
1.1 Atoms 1
1.2 Some Important Definitions 2
1.3 Electronic Configuration of an Atom 3
Quantum numbers 4
Aufbau principle 6
Pauli exclusion principle 8
Hund’s rule 9
Stability of half-filled and fully-filled shells 13
Electronic configuration of ions 13
Nodal planes of different orbitals 15
Slater’s rule 15
Single Correct Choice Type Questions 17
Multiple Correct Choice Type Questions 20
Comprehension Type Questions 21
Assertion-Reasoning Type Questions 23
Integer Answer Type Questions 23
Matrix-Match Type Questions 24
Answers 25
3. Chemical Bonding 59
3.1 Attainment of a Stable Configuration 60
3.2 Types of Bonds 60
3.3 Transitions Between the Main Types of Bonding 61
Ionic bonds 61
Covalent bonds 62
Oxidation numbers 63
Coordinate bonds 63
Double and triple bonds 64
Metallic bonds and metallic structures 64
3.4 The Covalent Bond 64
The Lewis theory 64
Sidgwick–Powell theory 66
3.5 Valence Bond Theory 66
What is the essence of hybridization? 66
Features of hybrid orbitals 67
Calculation of steric number 68
3.6 Valence Shell Electron Pair Repulsion (Vsepr) Theory 69
Effect of lone pair 69
Effect of double bond 73
Effect of electronegativity 73
Back bonding 75
3.7 The Extent of d Orbital Participation in Molecular Bonding 79
3.8 Types of Covalent Bonds (Sigma (s ) and Pi (p ) Bonds) 80
Bridge bonding 83
3.9 Molecular Orbital Method 85
3.10 Lcao Method 85
s–s combinations of orbitals 86
s–p combinations of orbitals 87
p–p combinations of orbitals 88
p–d combinations of orbitals 89
d–d combinations of orbitals 89
Non-bonding combinations of orbitals 89
3.11 Rules for Linear Combination of Atomic Orbitals 90
3.12 Examples of Molecular Orbital Treatment for Homonuclear Diatomic Molecules 92
H+2 molecule ion 93
H2 molecule 93
+
He2 molecule ion 93
He2 molecule 94
Li2 molecule 94
Be2 molecule 94
B2 molecule 94
C2 molecule 94
N2 molecule 95
O2 molecule 95
O-2 ion 95
F2 molecule 96
3.13 Examples of Molecular Orbital Treatment for Heteronuclear Diatomic Molecules 96
NO molecule 97
CO molecule 97
3.14 Dipole Moment 98
Application of dipole moment 100
Some special cases102
4. Hydrolysis 157
4.1 introduction 157
4.2 Hydrolysis Through SN1 Mechanism 157
4.3 Hydrolysis Through SN2 Mechanism 158
4.4 Hydrolysis Through Addition–Elimination Mechanism 162
4.5 Hydrolysis Through Addition Mechanism 163
4.6 Hydrolysis Through Redox Reaction 163
4.7 Hydrolysis Through Push–Pull Mechanism 163
4.8 Hydrolysis Through Mixed Mechanism 164
Single Correct Choice Type Questions 166
Multiple Correct Choice Type Questions 167
Comprehension Type Questions 167
Assertion–Reasoning Type Questions 168
Integer Answer Type Questions 169
Matrix–Match Type Questions 169
Answers 170
5. Coordination Compounds 171
5.1 Double Salts and Coordination Compounds 171
5.2 Werner’s Work 172
5.3 More Recent Methods of Studying Complexes 173
5.4 Classification of Ligands 175
5.5 Effective Atomic Number (EAN) 178
Sidgwick EAN rule 179
5.6 Shapes of d Orbitals 180
5.7 Bonding in Transition Metal Complexes 181
Valence bond theory 181
Crystal field theory 181
Molecular orbital theory 181
5.8 Valence Bond Theory 181
5.9 Crystal Field Theory 182
Octahedral complexes 183
5.10 Effects of Crystal Field Splitting 188
5.11 Tetragonal Distortion of Octahedral Complexes (Jahn-Teller Distortion) 189
5.12 Square Planar Arrangements 191
5.13 Tetrahedral Complexes 193
5.14 Magnetism 195
5.15 Extension of the Crystal Field Theory to Allow for Some Covalency 196
5.16 Nomenclature of Coordination Compounds 196
5.17 Isomerism 199
Polymerization isomerism 199
Ionization isomerism 199
Hydrate isomerism 199
Linkage isomerism 200
Coordination isomerism 200
Coordination position isomerism 201
Geometrical isomerism and optical isomerism 201
Single Correct Choice Type Questions 206
Multiple Correct Choice Type Questions 209
Comprehension Type Questions 210
Assertion–Reasoning Type Questions 211
Integer Answer Type Questions 212
Matrix–Match Type Questions 212
Answers 214
6. Metallurgy 217
6.1 Types of Ores 218
6.2 Principal Steps in the Recovery of a Metal from its Ore 219
6.3 Concentration or Dressing of Ore 219
Gravity separation or levigation 220
Magnetic separation 220
Froth floatation or oil floatation 220
Chemical method of separation: leaching 222
6.4 Conversion of Concentrated Ore into its Oxide 222
Calcination 222
Roasting 222
6.5 Different Reduction Processes 223
Carbon reduction 223
Self reduction 224
Thermite reduction (or Goldschmidt-Thermite process) 224
Metal replacement method (Hydrometallurgy) 225
Electrolytic reduction 225
Thermal decomposition method 226
6.6 Purification or Refining of Metal 226
Thermal refining 226
Electrorefining 228
6.7 Thermodynamics of Reduction Process 229
6.8 Alloys and Amalgams 231
Classification of alloys 231
Characteristics of alloys 232
Preparation of alloys 232
Amalgam 233
6.9 Different Types of Furnaces Used in Metallurgy 233
6.10 Extraction of Silver 234
Refining of Ag 235
6.11 Extraction of Gold by Cyanide Process 235
Refining of Au 235
6.12 Extraction of Tin 236
Refining of Sn 237
6.13 Extraction of Magnesium 237
Electrolytic reduction 237
Carbon reduction process 239
Other processes 239
6.14 Extraction of Aluminium 239
Beneficiation of bauxite 240
Electrolytic reduction of pure Al2O3 242
Electrorefining of aluminium 243
6.15 Extraction of Lead 244
Carbon reduction 244
Self reduction process 246
Refining of lead 246
6.16 Extraction of Copper 246
Refining of blister copper 248
6.17 Extraction of Zinc 248
6.18 Extraction of Iron 250
Purification of iron or preparation of wrought iron 251
Steel making 252
Single Correct Choice Type Questions 253
Multiple Correct Choice Type Questions 255
Appendices593–612
Appendix A Abundance of the Elements in the Earth’s Crust 593
Appendix B Melting Points of the Elements 595
Appendix C Boiling Points of the Elements 596
Appendix D Densities of the Solid and Liquid Elements 597
Appendix E Electronic Structures of the Elements 598
Appendix F Some Average Single Bond Energies and Some Double and
Triple Bond Energies 602
Appendix G Solubilities of Main Group Compounds in Water 603
Appendix H Atomic Weights Based on 12 C = 12.000 605
Appendix I Values of Some Fundamental Physical Constants 607
Appendix J Electrical Resistivity of the Elements at the Stated Temperature 608
Appendix K Hardness of Minerals – Mohs’ Scale 610
Index I1
1
Structure of an
Shells Possible subshells
n=1 1s
n=2 2s 2p
Atom n=3
n=4
3s
4s
3p
4p
3d
4d 4f
n=5 5s 5p 5d 5f 5g
n=6 6s 6p 6d 6f 6g
n=7 7s 7p
n=8 8s 8p
5. Isoelectronic species: The species having the same number of electrons are known as isoelectronic spe-
cies. (It may be an atom, ion or a molecule.) For example,
a. C 4- , N 3- , O2- , F- , Ne, Na + , Mg 2+ , Al 3+
b. Si 4− , P 3 − , S 2 − , Cl − , Ar, K + , Ca 2 + , Sc 3+
c. H 2 S, HCl, Ar, SH −
d. NH 2− , NH 3 , CH 4 , H 2 O, OH − , NH +4 , OH − , NH 2 −
Ni (CO)4 ], [ Co (CO)4 , Fe (CO)4 , Fe (CO)2 ( NO)2
− 2−
e.
f. CO23 − , NO−3 , BO33−
g. SiO44 − , PO34− , SO24 − , ClO4−
Now-a-days the definition of isoelectronic species is also observed to extend to include the species
having the same number of valence shell electrons (described later in the section on Classification of
elements as s, p, d and f-block elements). For example, the following species can also be considered
isoelectronic because they have the same number of valence shell electrons:
6. Isosters: Species that are isoelectronic as well as consist of the same number of atoms are known as
isosters. For example,
a. CH 4 , NH +4
b. CO23 − , NO−3 , BO33−
c. NH 2− , H 2 O
d. SiO44 − , PO34− , SO24 − , ClO4−
Quantum numbers
The characteristic features of the four quantum numbers are described as follows:
1. Principal quantum number (n): This quantum number indicates the distance of an electron from the
nucleus. It can have values of 1, 2, 3, 4 … up to ∞. As the value of n increases, the distance of the electron/
orbital from the nucleus increases as well as the energy of the electron increases.
Principal quantum numbers having different values of n are also considered as different energy
shells which are represented as follows:
n 1 2 3 4 5 6 7 …∞
Energy shells K L M N O P Q
2. Azimuthal quantum number (l): This quantum number indicates the shape of an orbital (not of elec-
tron) and can have values from 0 to (n–1) for a particular value of n. For example, for n = 5, the value
of l are 0, 1, 2, 3, 4.
Each value of l indicates the sub-energy level or subshell within the particular shell or energy level,
which are denoted as follows:
l 0 1 2 3 4
Subshell or sub-energy level s p d f g
Note: The notations for the sub-energy levels come from the spectroscopic terms that were used to
describe the atomic spectra and have the following full form:
s → sharp f → fundamental
p → principal
g → generalized
d → diffused
These subshells have different shapes which are depicted in Table 1.2.
or
(Continued)
Note:
(i) f and g subshells are of complicated shape and beyond the scope of syllabus.
(ii) These shapes of subshells are not experimentally observed as these are the 3D – plots of solution
of Schrödinger wave equation which is not part of the syllabus for JEE.
3. Magnetic quantum number (m or ml): This quantum number indicates the possible orientations of
an orbital in space. The value of m for a particular value of l varies from +l to –l including zero. For
example,
The different values of m for a particular value of l gives the possible orientations of the corresponding
orbital in space. Each possible orientation is considered as a particular orbital.
z z z
x x x
y y y
px py
pz
c. d-subshell consists of five orbitals that are known as dxy dyz, dxz, dx2 − y2 and dz2 which are shown in
Figure 1.3.
y z z
x x y
y
x x
dx 2 −y2 dz2
Note:
(i) dxy, dyz, dxz orbitals are known as non-axial d-orbitals because the lobes of the orbitals are not
available along the axis.
(ii) dx −y and dz are known as axial d-orbitals because the lobes of oribtals are along the axis.
2 2 2
4. Spin Quantum Number (s or ms): It is the quantum number which is required to describe an electron
only (not the orbital) and it characterizes the spin of an electron. An electron is not only moving
around the nucleus but also spinning about its own axis. It may spin either clockwise or anticlockwise.
a. The possible values of spin quantum number are +1/2 and −1/2, but it is not fixed, that is, if the value
of s is +1/2 for clockwise spinning, then the value of s is −1/2 for anticlockwise and vice-versa. Also,
the electrons present in parallel spin must have the same spin value, for example,
or
s = −1 2 −1 2 −1 2
or
s = +1/2 +1/2 +1/2
or
Aufbau principle
The electrons are filled up in the empty orbitals of an atom from the lowest energy orbital to the higher
energy orbital. The energy sequence of empty orbitals is given in Figure 1.4, in which the energy of the
subshells increases along the directions of arrow.
n=1 1s
n=2 2s 2p
n=3 3s 3p 3d
n=4 4s 4p 4d 4f
n=5 5s 5p 5d 5f 5g
n=6 6s 6p 6d 6f 6g
n=7 7s 7p
n=8 8s 8p
Alternatively, the above energy sequence or the energy comparison between any two subshells can be
established very easily on the basis of (n + l) rule which is stated as follows:
1. Smaller the value of (n + l) for a particular subshell smaller will be its energy.
2. If for two subshell, the (n + l) value is the same then the subshell having higher value of n will have
higher energy. For example,
for 3d ⇒ n + l = 3 + 2 = 5
same
and for 4 p ⇒ n + l = 4 + 1 = 5
Between the two, 4p has higher energy as compared to that of 3d.
Let us compare the energy of the following subshells according to (n + l) rule:
5p, 4s, 4d, 3d, 4f, 6s
Based on the (n + l) rule, we have
Subshell (n + l )
5p 5+1=6
4s 4+0=4
4d 4+2=6
3d 3+2=5
4f 4+3=7
6s 6+0=6
Hence the energy order will be: 4 f > 6 s > 5 p > 4d > 3d
(Continued)
–1
–2
–3
So on…
Note:
(i) The number of orbitals present in a subshell is (2l + 1).
(ii) The total number of electrons present in a subshell is 2(2l + 1).
(iii) Total number of orbitals present in a shell is n2.
(iv) Total number of electron present in a shell is 2n2.
Based on the above rules, let us find the number of subshell, orbitals and maximum number of electrons
that can be accommodated in R shell.
Shell K L M N O P Q R
n= 1 2 3 4 5 6 7 8
Hund’s rule
According to this rule, the degenerate orbitals (i.e. orbitals having same energy) will be filled by one electron
each having same spin and then only pairing of electrons will take place. Alternatively, the filling up of
electron in the degenerate orbitals will take place in such a way that the multiplicity (M) value will be maximum
where M is defined as follows:
M = 2 | S | +1
where S = total spin value of all electrons in degenerate orbitals.
For example, consider the nitrogen atom; the electronic distribution is shown as follows:
7 N : 1s2 2s2 2p3 M = 2|S| + 1
Using all the above discussed rules, that is, Aufbau principle, Pauli’s exclusion principle and Hund’s
rule, the electronic configuration of different elements can be written. For example,
12 Mg : 1s 2 2s2 2 p6 3s 2
31 Ga : 1s 2 2s2 2 p6 3s 2 3 p6 4s2 3d 10 4 p1
The electronic configuration of all the known elements is given in Table 1.4.
Table 1.4 Electronic configurations of elements
Element Atomic Subshells
number (Z ) Is 2s 2p 3s 3p 3d 4s 4p 4d 4f 5s 5p 5d 5f 6s 6p 6d 7s
H 1 1
He 2 2
Li 3 2 1
Be 4 2 2
B 5 2 2 1
C 6 2 2 2
N 7 2 2 3
O 8 2 2 4
F 9 2 2 5
Ne 10 2 2 6
Na 11 2 2 6 1
Mg 12 2 2 6 2
A1 13 2 2 6 2 1
Si 14 2 2 6 2 2
P 15 2 2 6 2 3
S 16 2 2 6 2 4
Cl 17 2 2 6 2 5
Ar 18 2 2 6 2 6
K 19 2 2 6 2 6 1
Ca 20 2 2 6 2 6 2
Sc 21 2 2 6 2 6 1 2
Ti 22 2 2 6 2 6 2 2
V 23 2 2 6 2 6 3 2
Cr* 24 2 2 6 2 6 5 1
Mn 25 2 2 6 2 6 5 2
Fe 26 2 2 6 2 6 6 2
Co 27 2 2 6 2 6 7 2
Ni 28 2 2 6 2 6 8 2
Cu* 29 2 2 6 2 6 10 1
Zn 30 2 2 6 2 6 10 2
Ga 31 2 2 6 2 6 10 2 1
Ge 32 2 2 6 2 6 10 2 2
As 33 2 2 6 2 6 10 2 3
Se 34 2 2 6 2 6 10 2 4
(Continued)
The (*) marked elements are those for which the Aufbau principle is not strictly followed.
Elements beyond the (**) marked element are also known. The elements with atomic numbers 112,
114 and 116 have been discovered and assigned official IUPAC names copernicium, fleuorium and
livermorium, respectively. The elements with atomic numbers 113, 115, 117 and 118 are yet to be
discovered.
44 Ru : [Kr] 5s1 4d 7
29 Cu : [Ar] 4 s1 3d 10 45 Rh : [Kr] 5s1 4d 8
47 Ag : [Kr] 5s1 4d 10 46 Pd : [Kr] 5s 0 4d 10
79 Au : [X e] 4 f 14 6s1 5d 10 78 Pt : [Xe] 6s1 4 f 14 5d 9
Several above violations of Aufbau principle can be explained on the basis of achieving either half-
filled or fully-filled configurations of a subshell which are relatively more stable. The extra stability of half-
filled and fully-filled configurations can be attributed to the following reasons:
1. The symmetry leads the stability (as the rule of nature).
2. The exchange energy is more for half-filled and fully-filled electronic configuration. For example, con-
sider the electronic configuration shown in Figure 1.5, in which the possible exchange of positions of
electrons is depicted.
4 + 3 + 2 + 1 = 10
After exchanging the position between any two electrons, it gives the same configuration. During this
exchange of position of electrons, some amount of energy is released which is known as exchange energy.
More number of exchanges causes release of more energy.
For the above case (i.e. d5 configuration), the total number of possible exchanges is ten. Similarly for d10
configuration, the total number of possible exchanges will be (10 + 10) = 20, (only two electron of same spin
are allowed to exchange their position). Hence, ten exchanges are possible for 5 electrons having +1/2 spin
and another ten exchanges are possible for five electrons having −1/2 spin. Hence fully-filled configuration
is more stable as compared to half-filled configuration.
If the atomic number of an atom A is Z, then total number of electrons in A– is (Z+ 1) and in A2− is
(Z + 2). Hence, to arrive at the electronic configuration, count the total number of electrons in the
anion and fill them in the empty orbital available in that element. For example, consider N 3− :
Total number of electrons = 7 + 3 = 10.
The electronic configuration is: 1s2 2s2 2p6.
2. For cation:
M −
e
→ M + −
e
→ M 2+
M −
xe
→M x+
Hence, the total number of electrons in Mx+ is = Z− x where Z is the atomic number of M.
Then write the electronic configuration as usual if M is an element of s-block or p-block.
But if M is an element of d-block or f-block, then write the electronic configuration of the respective
element M first and then remove the x number of electrons from ns, then from (n – 1)d and then from
(n – 2)f orbital gradually. For example, consider Fe and Cu ions for d-block elements.
(i)
Fe : [Ar]3d 6 4s 2
26
(ii)
Cu : [Ar] 3d 10 4 s1
29
Cu+ : [Ar] 3d 10 4 s 0
Cu 2+ : [Ar] 3d 9
Following the Hund’s rule, after obtaining the electronic configuration, the number of unpaired electrons
(if any) can be calculated for any element or ion. From the number of unpaired electrons, it can further
be predicted if the species is paramagnetic or diamagnetic. If we assume that the magnetic moment arises
entirely from unpaired electron spins, then the spin only magnetic moment value can be calculated using
the following formula:
where n is the number of unpaired electrons present in the species. Spin only magnetic moment is also
referred to as magnetic momentm for convenience sake.
1. Paramagnetic: The substance consisting of unpaired electron(s) (either one or more) is known as para-
magnetic and it is attracted by the magnetic field. Paramagnetic substances are coloured in general.
2. Diamagnetic: The substance consisting of no unpaired electron is known as diamagnetic and it is
repelled by the magnetic field. Diamagnetic substances are generally colourless.
Let us predict the magnetic behaviour of ions based on their electronic configurations. For example, con-
sider Mn2+, the electronic configuration is:
Mn : [Ar] 3d 5 4s2
Mn 2+ : [Ar] 3d 5 or
The electronic configuration shows the presence of five unpaired electrons, hence it is paramagnetic and
the magnetic moment (mS) is
mS = 5 ( 5 + 2 ) BM
= 35 B.M = 5.92 BM
DAUBER
THE SETTING OF THE WATCH
The watch was set, the night came, and the men
Hid from the moon in shadowed nooks to sleep,
Bunched like the dead; still, like the dead, as when
Plague in a city leaves none even to weep.
The ship’s track brightened to a mile-broad sweep;
The mate there felt her pulse, and eyed the spars:
South-west by south she staggered under the stars.
Rolled till she clanged, rolled till the brain was tired,
Marking the acme of the heaves, the pause
While the sea-beauty rested and respired,
Drinking great draughts of roller at her hawse.
Flutters of snow came aimless upon flaws.
“Lock up your paints,” the Mate said, speaking light:
“This is the Horn; you’ll join my watch to-night!”
“Whales!” said the mate. They stayed there all night long
Answering the horn. Out of the night they spoke,
Defeated creatures who had suffered wrong,
But were still noble underneath the stroke.
They filled the darkness when the Dauber woke;
The men came peering to the rail to hear,
And the sea sighed, and the fog rose up sheer.
And then the night fell dark, and all night long
The pointed mountain pointed at the stars,
Frozen, alert, austere; the eagle’s song
Screamed from her desolate screes and splintered scars.
On her intense crags where the air is sparse
The stars looked down; their many golden eyes
Watched her and burned, burned out, and came to rise.
THE RIVER.
The steaming river loitered like old blood
On which the tugboat bearing Michael beat,
Past whitened horse bones sticking in the mud.
The reed stems looked like metal in the heat.
Then the banks fell away, and there were neat;
Red herds of sullen cattle drifting slow.
A fish leaped, making rings, making the dead blood flow.
THE RETURN.
Soon he was at the Foxholes, at the place
Whither, from over sea, his heart had turned
Often at evening-ends in times of grace.
But little outward change his eye discerned;
A red rose at her bedroom window burned,
Just as before. Even as of old the wasps
Poised at the yellow plums; the gate creaked on its hasps
“S h ill k tl t th t h
“So she will know at least that she was wrong,
That underneath the blindness I was true.
Fate is the strongest thing, though men are strong;
Out from beyond life I was sealed to you.
But my blind ways destroyed the cords that drew;
And now, the evil done, I know my need;
Fate has his way with those who mar what is decreed.
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