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Structure of Atom Class 11 Notes: CBSE Chemistry Chapter 2

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Class 11 Chemistry Structure of Atom Notes PDF Download

Chapter 2 Structure of Atom of Class 11 Chemistry explains the foundational concepts of atomic structure, focusing on the models and theories that describe how atoms are structured. This chapter covers the fundamental particles of the atom, atomic models, and the principles governing atomic behaviour. Understanding these concepts is crucial for giving insights into more complex topics in chemistry, as they provide the basis for comprehending how elements interact and bond to form compounds.


The structure of Atom Class 11  Notes lets you quickly access and review the chapter content. For a comprehensive study experience, check out the Class 11 Chemistry Revision Notes FREE PDF here and refer to the CBSE Class 11 Chemistry Syllabus for detailed coverage. Vedantu's notes offer a focused, student-friendly approach, setting them apart from other resources and providing you with the best tools for success. 

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Access Class 11 Chemistry Chapter 2 - Structure of Atom Notes

S.No

Common Name                  

Chemical Name                         

Formulae

1

Alum

Hydrated double sulphate   of potassium and aluminium             

K2SO4 .Al2(SO4)3 .24H2O

2

Alumina

Aluminium oxide

Al2O3

3

Ammonia water              

Ammonium hydroxide                       

NH4OH

4

Angelsite

Lead sulphate

PbSO4

5

Aqua fortis                     

Concentrated nitric acid                   

HNO3

6

Aqua regia


3HCl(Conc) +  HNO3(Conc)

7

Azote gas  

Nitrogen

N2

8

Azurite blue                       

Basic copper carbonate    

2CuCO3.Cu(OH)2

9

Baking Soda                   

Sodium hydrogen carbonate              

NaHCO3

10

Baryta

Barium Hydroxide                               

Ba(OH)2

11

Basic lead acetate

-

Pb(OH)2Pb(CH3COO)2

12

Bauxite

Dihydrate Aluminium oxide                 

Al2O3 .2H2O

13

Blue Vitriol                       

Pentahydrate of cupric sulphate         

CuSO4 .5H2O

14

Bleaching powder             

Calcium oxychloride or calcium  (hypochlorite) chloride                                                        

CaOCl2 or Ca(OCl)Cl

15

Borax

Sodium tetraborate                              

Na2B4O7 .10H2O

16

Brimstone

Sulphur

S

17

Brine or common salt          

Sodium Chloride                               

NaCl or rock salt

18

Cerussite   

Lead carbonate                                

PbCO3

19

Chalk or limestone             

Calcium Carbonate

CaCO3

20

Chile saltpetre of Caliche     

Sodium nitrate                                  

NaNO3

21

Cuprite or ruby copper           

Cuprous oxide                                   

Cu2O

22

Copper glance                     

Copper sulphide                               

Cu2S

23

Carnallite

Potassium magnesium chloride        

KCl.MgCl2 .6H2O

24

Calomel

Mercurous chloride 

Hg2Cl2

25

Cane sugar or Beet sugar      

Sucrose

C12H22O11

26

Calgon

Sodium hexa-metaphosphate          

Na2[Na4(PO3)6]

27

Caustic soda                      

Sodium hydroxide                               

NaOH

28

Caustic potash                     

Potassium hydroxide                          

KOH

29

Calamine

Zinc carbonate                                     

ZnCO3

30

Corundum

Aluminium oxide                                  

Al2O3

31

Dead burnt gypsum         

Anhydrous calcium sulphate             

CaSO4

32

Diaspore Monohydrate    

aluminium oxide

Al2O3 .H2O

33

Dry ice Solid                       

carbon dioxide                                  

CO2 (solid)

34

Epsom salt                    

Heptahydrate of magnesium sulphate                              

MgSO4 .7H2O

35

Fluorspar

Calcium fluoride                                    

CaF2

36

Galena

Lead sulphide

PbS

37

Glauber’s salt

Hydrated sodium sulphate

Na2SO4 .10H2O

38

Green Vitriol

Ferrous sulphate

FeSO4 .7H2O

39

Gypsum

Calcium sulphate dihydrate

CaSO4 .2H2O

40

Hydrolith

Calcium hydride

CaH2

41

Hypo

Sodium thiosulphate

Na2S2O3 .5H2O

42

Iron pyrites

Iron disulphide

FeS2

43

Laughing gas

Dinitrogen oxide

N2O

44

Limonite

Hydrated ferric oxide

Fe2O3 .3H2O

45

Litharge

Lead monoxide

PbO

46

Lime

Calcium oxide

CaO

47

Lime water or slaked lime

Calcium hydroxide

Ca(OH)2

48

Limestone or chalk or marble

Calcium carbonate

CaCO3

49

Lunar caustic

Silver nitrate

AgNO3

50

Magnetite

Ferrosoferric oxide

Fe3O4

51

Milk of lime

Calcium hydroxide

Ca(OH)2

52

Milk of magnesia

Magnesium hydroxide

Mg(OH)2

53

Marsh gas

Methane

CH4

54

Malachite (green)

Basic copper carbonate

CuCO3 .Cu(OH)2

55

Magnesia

Magnesium oxide

MgO

56

Magnesite

Magnesium carbonate

MgCO3

57

Mohr’s salt

Ferrous ammonium sulphate hexahydrate

(NH4) 2SO4 FeSO4 .6H2O

58

Muriatic acid

Hydrochloric acid

HCl

59

Nessler’s reagent

Potassium tetra-idomercurate

K2[Hg I4]

60

Nitre

Potassium nitrate

KNO3

61

Nitre cake

Sodium hydrogen sulphate

NaHSO4

62

Nitrolim

Calcium cyanamide plus carbon

CaCN2 +  C

63

Nitrate of lime (Nitrolime)

Basic calcium nitrate

Ca(NO3)2 .CaO

64

Oil of Vitriol

Concentrated Sulphuric acid

H2SO4

65

Oleum

Pyrosulphuric acid

H2S2O7

66

Pearl ash

Potassium carbonate

K2CO3

67

Philosopher’s wool

Zinc oxide

ZnO

68

Phosgene

Carbonyl chloride

COCl2

69

Potash

Potassium carbonate

K2CO3

70

Potash alum

Potassium aluminium sulphate

K2SO4 .Al2(SO4)3 .24H2O

71

Plaster of Paris

Hemihydrate of calcium sulphate

CaSO .12 H2O

72

Pyrogallol

Benzene-1, 2, 3-triol

C6H3(OH)3

73

Pyrolusite

Manganese dioxide

MnO2

74

Quartz or silica

Silicon dioxide

SiO2

75

Quick lime

Calcium oxide

CaO

76

Quicksilver

Mercury

Hg

77

Red lead

Triplumbic tetroxide

Pb3O4

78

Rock salt

Sodium chloride

NaCl

79

Rough

Ferric oxide

Fe2O3

80

Sal ammoniac Solid

ammonium chloride

NH4Cl

81

Sal volatile Solid

ammonium carbonate

(NH4)2CO3

82

Salt cake

Anhydrous sodium sulphate

Na2SO4

83

Saltpetre

Potassium nitrate

KNO3

84

Siderite

Ferrous carbonate

FeCO3

85

Silica

Silicon dioxide

SiO2

86

Silica gel

Hydrated silica

SiO2 , xH2O

87

Slaked lime

Calcium hydroxide

Ca(OH)2

88

Soda ash

Anhydrous sodium carbonate

Na2CO3

89

Water glass

Sodium dioxide containing excess of silica

Na2SiO3 .SiO2

90

Super phosphate of lime

Mixture of calcium dihydrogen phosphate and calcium sulphate

Ca(H2PO4)2 .H2O  +  2CaSO4 .2H2O

91

Verdigris Basic

copper acetate

Cu(CH3COO)2

92

White lead

Basic lead carbonate

2PbCO3 .Pb(OH)2

93

White Vitriol

Heptahydrate of zinc sulphate

ZnSO4 .7H2O

94

Washing soda

Hydrated sodium carbonate

Na2CO3 .10H2O

95

Zincite

Zinc oxide

ZnO

96

Zinc blende

Zinc sulphide

ZnS


VALENCY OF SOME COMMON BASIC AND ACIDIC RADICALS

Electrovalent Positive Ions (Basic Radicals)


Monovalent


1

Ammonium

NH4 + 

2

Aurous [Gold (I)]

Au + 

3

Cuprous [Copper (I)]

Cu + 

4

Hydrogen

H + 

5

Mercurous [Mercury (I)]

Hg + 

6

Potassium

K + 

7

Sodium

Na + 

8

Argentous [Silver (I)]

Ag + 

9

Lithium

Li + 



Divalent


1

Argentic [Silver(II)]

Ag2 + 

2

Barium

Ba2 + 

3

Calcium

Ca2 + 

4

Cupric [Copper(II)]

Cu2 + 

5

Ferrous [Iron (II)]

Fe2 + 

6

Magnesium

Mg2 + 

7

Mercuric [Mercury (II)]

Hg2 + 

8

Plumbous [Lead (II)]

Pb2 + 

9

Stannous [Tin (II)]

Sn2 + 

10

Zinc

Zn2 + 

11

Platinous [Platinum (II)]

Pt2 + 

12

Nickel

Ni2 + 



Trivalent


1

Aluminium

Al3 + 

2

Ferric [Iron (III)]

Fe3 + 

3

Chromium

Cr3 + 

4

Auric [Gold (III)]

Au3 + 

5

Bismuth

Bi3 + 

6

Arsenic

As3 + 



Tetravalent


1

Plumbic [Lead (IV)]

Pb4 + 

2

Stannic [Tin (IV)]

Sn4 + 

3

Platonic [Platinium (IV)]

Pt4 + 


ELECTROVALENT NEGATIVE IONS (ACIDIC RADICALS)


Monovalent


1

Acetate

CH3COO--

2

Bicarbonate or Hydrogen carbonate

HCO3--

3

Bisulfite or Hydrogen sulphide

HS--

4

Bisulphate or Hydrogen sulphate

HSO4 --

5

Bisulfite or Hydrogen sulphite

HSO3 --

6

Bromide

Br--

7

Chloride

Cl--

8

Permanganate

MnO4 --

9

Fluoride

F --

10

Hydride

H--

11

Hydroxide

OH--

12

Iodide

I--

13

Cyanide

CN--

14

Nitrate

NO3--

15

Nitrite

NO2 --

16

Chlorite

ClO2 --

17

Hypochlorite

ClO--

18

Chlorate

ClO3--

19

Perchlorate

ClO4 --

20

Meta aluminate

AlO2



Divalent


1

Carbonate

CO3 2--

2

Dichromate

Cr2O72--

3

Oxide

O2--

4

Peroxide

O22--

5

Sulphate

SO42--

6

Sulphite

SO32--

7

Sulphide

S2--

8

Silicate

SiO32--

9

Thiosulphate

S2O32--

10

Zincate

ZnO22--

11

Plumbite

PbO22--

12

Stannate

SnO32--

13

Manganate

MnO42--

14

Chromate

CrO42--

15

Oxalate

(COO)22--



Trivalent


1

Arsenate

AsO43--

2

Nitride

N3--

3

Arsenite

AsO33--

4

Phosphide

P3--

5

Phosphite

PO33--

6

Phosphate

PO43--

7

Borate

BO33--

8

Aluminate

AlO33--



Tetravalent


1

Carbide

C4--

2

Ferrocyanide

Fe(CN)64--


1. INTRODUCTION

This chapter delves into the mysterious and surprising world of atoms on the inside. Atoms and their structures underpin all of chemistry. We'll also look at how electrons behave and the repercussions of their actions.


1.1 Discovery of fundamental particles

Dalton's atomic theory was successful in explaining the laws of conservation of mass, constant composition, and multiple proportion, but it failed to explain the results of numerous tests, such as the fact that solids like glass or ebonite create electricity when touched with silk or fur.


1.1.1 Electron discovery Of 1879, William Crookes investigated the electrical discharge in cathode ray discharge tubes, which are partially evacuated tubes. A discharge tube is a glass tube that is roughly 60cm long and has two thin metal bits called electrodes that are sealed inside. Crooke's tube is the name for this type of tube. The negative electrode is referred to as the cathode, whereas the positive electrode is referred to as the anode.

Invisible rays emanating from the cathode and producing a greenish light behind the perforated anode on the glass wall coated with phosphorescent substance ZnS are detected when a gas is confined at low pressure (10-4 atm) in a discharge tube is subjected to a high voltage (10,000V).


Cathode Ray Experiment


Cathode Ray Experiment


Cathode rays were the name given to these beams.


1.1.2 Characteristics

1. They cast a sharp shadow on solid objects in their route, implying that they are travelling in a straight line.

2. They are negatively charged because they are redirected towards the positive plate in an electric field. Stoney gave them the name electrons.

3. They can make a light paddle wheel that rotates in front of them. They have kinetic energy and are material particles, which means they have kinetic energy.

4. Their charge-to-mass ratio is 1.75882 1011C/kg.

5. They ionise the gases they pass through.

6. When they collide with a metallic target, they emit X-rays.

7. The material of the electrodes and the nature of the gas present in the cathode ray tube have no effect on the characteristics of cathode rays (electrons).


As a result, we can conclude that electrons are the fundamental building blocks of all matter.


1.1.3 Charge to mass ratio of electron


J.J. Thomson Experiment-Charge to Mass Ratio of Electron


J.J. Thomson Experiment-Charge to Mass Ratio of Electron


J.J. Thomson used a cathode ray tube to measure the e/m ratio of electrons in 1897, employing electric and magnetic fields that were perpendicular to each other and to the path of electrons.


In the presence of an electric or magnetic field, the extent to which electrons deviate from their path is determined by: 


(a) the charge on the electron,

(b) the mass of the particle, and 

(c) the strength of the electric or magnetic field.


The electrons are deflected to point A when merely an electric field is applied. Electrons are deflected to point C when merely a magnetic field is provided. The electrons can hit the screen at point B by balancing the intensities of electric and magnetic fields.


1.1.4 Charge on the electron

To establish the charge on the electrons, R.A Millikan invented the oil drop experiment.


Millikan Invented the Oil Drop Experiment


Millikan Invented the Oil Drop Experiment


Oil droplets in the form of mist were permitted to enter through a tiny hole in the upper plate of the electrical condenser in this manner. Through a microscope with a micrometre eye piece, the downward motion of these droplets was observed. Millikan was able to determine the mass of oil droplets by monitoring the velocity at which they fell. By passing an X-ray beam through the air inside the chamber, it was ionised. Collisions with gaseous ions gave these oil droplets their electrical charge.


Depending on the charge on the droplets and the polarity and strength of the voltage given to the plate, the fall of these charged oil droplets can be slowed, accelerated, or made immobile. Millikan discovered that the magnitude of electrical charge, q, on oil droplets is always an integral multiple of the electrical charge, e, by carefully monitoring the effects of electrical field intensity on the motion of oil droplets, q = n e, where n = 1, 2, 3…


The electron's charge is measured to be –1.6022 10–19C.

As a result, the mass of an electron was computed as

m = ee/m=1.6022×1019C1.758820 1011C/ kg=9.1094 1031 kg


1.1.5 Where do cathode rays come from?

Because the gas molecules are bombarded by the high-speed electrons discharged initially from the cathode, cathode rays are produced first from the cathode material and subsequently from the gas inside the discharge tube.


1.2.1 Proton discovery

Because the atom is electrically neutral as a whole and the presence of negatively charged particles has been proved, it was assumed that some positively charged particles must also be present. As a result, during his research with cathode rays, physicist Goldstein devised a unique discharge tube. Canal rays are a new type of ray that he found.


Canal rays get their name from the fact that they move in the opposite direction of cathode rays in a vacuum tube, passing through and emerging from a canal or hole in the cathode.


Anode rays are another name for them.


1.2.2 Properties:

They travel in straight lines for the most part.


2. They have a positive charge on them.

3. They are formed up of particles of substance.

4. The charge on the particles that make up anode rays is discovered to be dependent on the type of gas used.

5. It is discovered that the mass of the particles that make up anode rays is affected by the type of gas used.

6. The particle's charge to mass ratio (e/m) is discovered to be dependent on the gas used.

7. Their behaviour in electric and magnetic fields is diametrically opposed to that of electrons.


1.2.3 Origin of anode rays: Anode rays are thought to be created when high-speed electrons from cathode rays strike gaseous atoms, knocking away their electrons. These anode rays are formed in the space between the anode and the cathode and are not released by the anode.


When hydrogen was used as the discharge gas, the lightest charged particles were obtained. These particles have the highest e/m value. They had the smallest mass and a single positive charge. A proton was the name given to the particle.


A proton's charge is +1.6022×1019C

Mass of a proton = 1.672×1027kg


1.3.1 Neutron discovery

Rutherford proposed the theoretical requirement for the existence of a neutron particle in the atomic nucleus in 1920.


It was postulated that it be a neutral particle with a mass nearly equivalent to that of a proton. It was given the name neutron by him. Chadwick established its existence in 1932. When a beam of particles 2 4 (He) collided with Beryllium (Be), he saw that a new sort of particle was ejected. It was virtually the same mass as a proton (1.674 10–27kg) and had no charge.


511B + 24He714N + 01n49Be + 24He612C + 01n


ATOMIC BUILDING BLOCKS

Name

Discoverer

Symbol

Charge

Relative Charge

Mass

Electron

J.J. Thomson

e

1.6022×1019C

1

9.1094×1031Kg

Proton

Goldstein

P

+1.6022×1019C

+1

1.6726×1027Kg

Neutron

Chadwick

n

0

0

1.6749×1027Kg


2. DEFINITIONS

2.1 Electron

A basic particle with a mass almost equivalent to 1/1837th of that of a hydrogen atom and one unit negative charge.


2.2 Proton

A basic particle with a mass almost equal to that of a hydrogen atom and one unit positive charge.


2.3 Neutron

A fundamental particle with a mass almost equal to that of a hydrogen atom but no charge.


3. MODEL THOMSON

Sir J. J. Thomson, the inventor of the electron, was the first to propose an atomic structure model.


(I) Electrons are found in every atom.

(ii) The entire atom is neutral. The total positive and negative charges must be the same.

He saw the atom's positive charge being evenly distributed around an atomic-sized sphere (about 10–10 m in diameter). The electrons were tiny particles with a negative charge equal to the positive charge in the atom when they were grouped together. They were like plums in a dessert, embedded in the atom. The charge distribution was such that the arrangement was the most stable. The plum - pudding model of the atom was popular at the time. Also available are the raisin pudding and watermelon models.


Plum - Pudding Model of the Atom


Plum - Pudding Model of the Atom


3.1 Drawbacks

Though the model was able to explain the atom's overall neutrality, it was unable to explain Rutherford's scattering experiments satisfactorily.


4. RUTHERFORD’S α-SCATTERING EXPERIMENT

In 1909, Rutherford conducted particle scattering experiments. A fine stream of alpha particles bombards an extremely thin gold foil (0.004nm) in this experiment. Behind the gold foil is a fluorescent screen (ZnS), on which points emerging from-particles were captured.


Polonium was employed as the -particles' source.


Rutherford’s α-Scattering Experiment


Rutherford’s α-Scattering Experiment


4.1 Observations

Rutherford conducted a series of tests utilising particle scattering by an extremely thin gold foil.


The following observations were made: 


(i) The majority of the particles (99 percent) pass through it without deflection or deviation.

(ii) Particles were deflected at tiny angles in several cases.

(iii) Only a few particles were deflected by considerable angles, and one particle was deflected by 180o on rare occasions.


4.2 Conclusions

(i) Because most particles flowed through it without deflection, an atom must be exceedingly hollow and made up mostly of empty space.

(ii) Only a few particles were deflected significantly. This means that: (a) Electrons cannot deflect heavy and positively charged particles due to their negative charge and low mass.

(b) There must be an extremely hefty and positively charged body in the atom, such as the nucleus, that prevents positively charged particles from passing through.

(c) Because the number of particles that experience 180o deflection is so small, the volume of a positively charged body must be a very small proportion of the atom's overall volume. This positively charged substance must be at the nucleus, which is the centre of the atom.


Scattering of  α-Particles


Scattering of  α-Particles


The radius of an atom is found to be in the range of 10–10m, while the radius of the nucleus is in the range of 10–15m. If a cricket ball represents a nucleus, the radius of an atom is around 5 kilometres5.3.1 Isotopes

.


4.3 Rutherford’s nuclear atomic model


Rutherford’s Nuclear Atomic Model


Rutherford’s Nuclear Atomic Model


(i) At the centre of an atom lies a tiny positively charged nucleus, which is surrounded by a hollow region known as the extra nuclear part.

(ii) Nucleons, which are made up of protons and neutrons, give the nucleus its positive charge, whereas electrons, which are found in the extra nuclear region, have minimal mass, and carry a negative charge.

(iii) Because the number of electrons in the atom equals the number of protons, it is electrically neutral. As a result, the nucleus' total positive charge is balanced by the electrons' total negative charge.

(iv) In the extranuclear section, electrons orbit the nucleus in circular routes known as orbits. As a result, an atom mimics the solar system, with the sun acting as the nucleus and the planets acting as circling electrons, and the model is referred to as the planetary model.

(v) The electrostatic force of attraction holds electrons and nuclei together.

(vi) Centrifugal forces perfectly balance the forces of attraction acting on the electron.


4.4 Drawbacks


Drawbacks of Rutherford’s Nuclear Atomic Model


Drawbacks of Rutherford’s Nuclear Atomic Model


(i)Any charged entity in motion under the influence of attractive forces should radiate energy continually, according to classical mechanics. If this is the case, the electron will spiral and eventually fall into the nucleus, causing the structure to collapse. This type of behaviour is never seen.

(ii) It contains no information on the electronic structure of atoms, such as how electrons are dispersed around the nucleus and their energies.


5. ATOMIC NUMBER AND MASS NUMBER

5.1 Atomic number (Z)

The number of unit positive charges or protons contained in the nucleus of an element's atom is equal to the element's atomic number. It also represents the neutral atom's number of electrons. For example, the number of protons in Na is 11, hence the atomic number of Na is 11.


5.2 Mass number (A)

The nucleons are the elementary particles (protons and neutrons) that make up the nucleus of an atom.


An atom's mass number (A) is equal to the total of its protons and neutrons. It's always a number that's a whole number. As a result, the mass number (A) equals the sum of the number of protons (Z) and the number of neutrons (N)


Therefore, number of neutrons (n) = Mass Number (A) – Number of protons (Z) n = A – Z


The general notation that is used to represent the mass number and atomic number of a given atoms is ZAX

Where, X symbol of element

A - Mass number

Z atomic number


5.3 Isotopes, Isobars, isotones and Isoelectronic

5.3.1 Isotopes: Isotopes are the same atomic number but different mass number atoms of the same element. The discrepancy is due to the number of neutrons present.


The number of electrons in an atom determines its chemical characteristics. As a result, isotopes of the same element have the same chemical behaviour.


Isotopes of Hydrogen


Isotope Mass 

Formula

Mass number 

No. of protons

No. of neutrons

Protium

11H(H)

1

1

0

Deuterium

12H(D)

2

1

1

Tritium

13H(T)

3

1

2


Isotopes of Oxygen


Isotope number

Mass number 

No. of protons

No. of neutrons

816O

16

8

8

817O

17

8

9

818O

18

8

10


Isotopes of Some Common Elements


Element 

Isotopes

Carbon (C)

612C,613C,614C

Nitrogen (N)

714N,715N

Uranium

92233U,92235U,92238U

Sulphur

1632S,1633S,1634S,1636S


5.3.2 Relative Abundance: In nature, varying percentages of an element's isotopes occur, which is referred to as relative abundance.


The average atomic mass of the element can be estimated using this relative abundance. Cl, for example, has an average atomic mass of 35.5 due to the presence of two isotopes, 35Cl and 37Cl, which are found in 75 percent and 25% abundance, respectively.


5.3.3 Isobars: Isobars are atoms of various elements with distinct atomic numbers but the same mass numbers.


Isobar

Atomic Number 

Mass Number 

No. of Electrons

No. of Protons

No. of Neutrons

1840Ar

18

40

18

18

22

1940K

19

40

19

19

21

2040Ca

20

40

20

20

20


5.3.4 Isotones: Isotones are atoms of various elements that have the same number of neutrons.


Isobar

Atomic Number 

Mass Number 

No. of Neutrons

1636S

16

36

20

1737Cl

17

37

20

1838Ar

18

38

20

1939K

19

39

20

2040Ca

20

40

20


5.3.5 Isoelectronic: This term refers to species (atoms or ions) that have the same number of electrons. For example, O2--F-- , Na +  , Mg + 2, Al + 3, Ne, and so on.


To go deeper into the atomic secrets, we'll need to learn about electromagnetic radiations and Maxwell's Electromagnetic Wave Theory."


The first thorough description of the interaction between charged things and the behaviour of electric and magnetic fields was given by James Maxwell.


To go deeper into the atomic secrets, we'll need to learn about electromagnetic radiations and Maxwell's Electromagnetic Wave Theory."


The first thorough description of the interaction between charged things and the behaviour of electric and magnetic fields was given by James Maxwell.


6. ELECTROMAGNETIC RADIATIONS

Waves created by oscillating magnetic and electric fields that are perpendicular to each other and both perpendicular to the direction of motion are known as electromagnetic radiation.


Electromagnetic Wave Graph


Electromagnetic Wave Graph


They do not require any medium and, unlike sound waves, can move in a vacuum.

Light is a type of radiation with wave properties.


The following are some of the characteristics of a wave:

1) Amplitude: The height of a wave's crest or trough (depth). metre (metric) (m)

2) Frequency: The number of waves that travel through a certain place in a second. Hertz (Hz) or s–1 are the units of measurement.

3) Time Period: A wave's period is the amount of time it takes to complete one vibration. time in seconds

4) Velocity: The velocity of a wave is the distance it travels in one second. m/s is the unit of speed.

All types of electromagnetic radiation travel at the same speed in vacuum, which is 3 108 m/s. This is known as the speed of light.

5) Wavelength(: A wavelength is the distance between two consecutive crests or troughs. Angstrom() [1=10–10m] is a unit of measurement.

6) Wave Number: This is the number of wavelengths per centimetre. m-1 is the unit of measurement.

ν=1/λ


6.1 Relationship between Velocity, Frequency & Wavelength

c = ν.λ

c: speed of light i.e. 3 × 108 m/s in vaccum 

ν: frequency;

 λ : wavelength


7. ELECTROMAGNETIC SPECTRUM

The electromagnetic spectrum is the band of radiations created when all electromagnetic radiations are grouped in ascending order of wavelength or decreasing frequency.


Electromagnetic Spectrum


Electromagnetic Spectrum 


The visible spectrum (VIBGYOR) is a subset of this spectrum with a wavelength range of 380-760 nm.


In this order, the wavelengths increase:

Gamma Rays < X-rays < Ultra-violet rays < Visible< Infrared < Micro-waves


7.1 Electromagnetic Wave Theory

(1) A source (such as a heated rod) emits energy continuously in the form of radiations (i.e., there is no change in wavelength or frequency of the emitted radiations as the energy radiated increases).

(2) These are electromagnetically emitted radiations.


7.2 Failure of EM wave theory

Two experiments shattered the theory:


(1) Black Body Radiation: According to Maxwell's theory of body heating, the intensity, or the amount of energy radiated per unit area, should grow without affecting the wavelength or frequency.


However, we notice that when we heat an iron rod, it turns red, then white, and finally blue at extremely high temperatures. The frequency of radiated radiations is shifting because of this.


A black body is an ideal body that produces and absorbs radiation of all frequencies, and the radiation emitted by a black body is known as black body radiation.


The intensity of a black solid varies with wavelength at different temperatures, as seen below:


Variation of Intensity of a Black Solid Vs Wavelength at Different Temperatures


Variation of Intensity of a Black Solid Vs Wavelength at Different Temperatures


As a result, as the temperature rises, the predominate wavelength in the emitted radiations drops while the frequency rises.


At greater temperatures, the intensity increases as predicted by Maxwell's theory, but the wavelength shortens. If T1>T2>T3, the answer is λ1<λ2<λ3.


Photoelectric Effect No. 2

When radiations with a specific minimum frequency (0) strike a metal's surface, electrons are expelled from the metal's surface. The photoelectric effect is the name for this phenomenon. Photoelectrons are the electrons that are released.


According to Maxwell's Theory, electron ejection should be dependent on the intensity of radiation; if electrons are not ejected, raising the intensity will allow them to be ejected.


Photoelectric Effect


Photoelectric Effect


Following are some observations:

(i) The electrons are ejected from the metal surface as soon as the light beam impacts it, i.e. there is no time lag between the light beam impacting the metal surface and the ejection of electrons.

(ii) The intensity or brightness of light is related to the number of electrons ejected.

(iii) There is a distinctive minimum frequency, 0 (also known as threshold frequency), below which no photoelectric effect is detected for each metal. The expelled electrons have a particular kinetic energy when the frequency is greater than zero. The kinetic energy of these electrons grows as the frequency of light utilised increases.


As a result, these observations ran counter to Maxwell's theory. The number of electrons ejected, and the accompanying kinetic energy should be proportional to the intensity of light. Although the number of electrons emitted is proportional to the brightness of the light, the kinetic energy of the ejected electrons is not.


Max Von Planc's Quantum theory was developed to support these discoveries.


8. PLANCK’S QUANTUM THEORY

The essential points of this theory are:

(i) Energy is emitted or absorbed discontinuously in the form of small discrete packets of energy rather than constantly. A 'quantum' is the name given to each such energy packet.


This quantum of energy is known as a photon in the case of light.


Planck’s Quantum Theory: Energy is Emitted or Absorbed Discontinuously inthe Form of Small Discrete Packets of Energy Rather than Constantly


Planck’s Quantum Theory: Energy is Emitted or Absorbed Discontinuously in the Form of Small Discrete Packets of Energy Rather than Constantly


(ii) Only one photon can be delivered to one electron or other particle at a time.

(iii) It is impossible to divide or distribute a quantum.

(iv) The frequency of radiation is precisely proportional to the energy of each quantum.

Eαν or E = hv = hcλ

h = Planck’s constant = 6.626×1034Js

(v) A body's total energy emitted or absorbed will be quantified in whole numbers.

E = nhv = nhcλ


This is also known as "energy quantisation."


8.1 Explanation of Black Body Radiation

The energy emitted increases as the temperature rises, increasing the frequency of the emitted radiations.


The wavelength moves to lower values as the frequency rises.


8.2 Explanation of Photoelectric effect

(i) When a photon of a specific frequency strikes the surface of a metal atom, it imparts all its energy to the metal atom's electron. Only if the photon's energy is high enough to overcome the nucleus's attraction to the electron will the electron be ejected from the metal. As a result, photoelectrons are only expelled when the input light has a minimal frequency (threshold frequency 0). The "Work Function," which is "h0," is the threshold energy necessary for emission.

(ii) If the incident light's frequency (v0) exceeds the threshold frequency (v0), the surplus energy is transferred to the electron as kinetic energy.

Energy of one quantum = Threshold Energy + Kinetic Energy

hv=hv0 + (1/ 2)mcv2 

(iii) When, the number of quanta incident increases as the intensity increases, resulting in an increase in the number of photoelectrons expelled.

(iv) When v0>v, the energy of each photon increases, and consequently the kinetic energy of each ejected electron grows as the frequency is increased.


Note:

Energy can also be expressed in Electron Volt(eV).


The energy acquired by an electron when it is accelerated through a potential difference of one volt.


1eV=1.602×1019J


CONCLUSION:

(iii) When, the number of quanta incident increases as the intensity increases, resulting in an increase in the number of photoelectrons expelled.

(iv) When v0>v, the energy of each photon increases, and consequently the kinetic energy of each ejected electron grows as the frequency is increased.


9. WHAT IS SPECTRUM?

A spectrum is a group or band of wavelengths/colors, and spectroscopy is the study of emission or absorption spectra.


9.1 Types of spectrum

Types of spectrums are

1) Emission Spectrum 

2) Absorption Spectrum


9.2 Emission Spectrum

When rays from a source strike a prism and are split into distinct wavelengths before being recorded on a photographic plate.


(a) Continuous Emission Spectra: There are no pauses between wavelengths, and one merges into the next.


Continuous Emission Spectra of White Light


Continuous Emission Spectra of White Light


Discontinuous Emission Spectra, also known as Line Spectra or Atomic Spectra, are a type of continuous emission spectrum.


Certain wavelengths are missing from a group, leaving dark areas in between, causing the spectrum to be discontinuous. It's also known as an element's fingerprint.


Line Spectrum Produced Form a Volatile Salt Placed in a Flame


Line Spectrum Produced Form a Volatile Salt Placed in a Flame


9.3 Absorption Spectra

When light from any source is first passed through the solution of a chemical substance and then analysed, it is observed that there are some dark lines in the otherwise continuous spectra.


Absorption spectrum


Absorption spectrum


Bohr researched the atomic spectra of hydrogen and offered his hypothesis based on his findings.


10. BOHR’S MODEL

10.1 Postulates

1) An atom is made up of a small, heavy, positively charged nucleus at the centre, which is surrounded by electrons in circular orbits.

2) Electrons can only revolve in orbits with a predetermined energy value. As a result, these orbits are referred to as "energy levels" or "stationary states."


1,2,3,... are the numbers assigned to them. Principal Quantum Numbers are the names given to these numbers.


(a) An electron's energy is given by:

En=--RH(Z2/n2)n  =  1,2,3.......

where RH is Rydberg’s constant and its value is 2.18 × 10–18 J.

Z = atomic number


En=2.18×1018Z2n2J/atom

  En=13.6Z2n2eV/atom

 En=1312Z2n2kJ/mol


As a result, the energies of various levels are arranged in the following order: K L M N...... and so on.


The energy of the lowest state (n=1) is referred to as ground state energy.


(b) Stationary state radiuses:

rn=52.9n2Z2pm

The radius of the first stationary state for an H-atom (Z = 1) is known as the Bohr orbit (52.9 pm)


(c) Electron velocities in different orbits: 

vn=2.188×102nm/s


3) Because electrons can only rotate in orbits with fixed energy values, electrons in an atom can only have certain certain energy values and not any of their own. An electron's energy is so quantified.

4) An electron in an atom's angular momentum, like its energy, can take on specific definite values and not any value at all.

mvr = nh2π

Where n=1,2,3...... 


5) When an electron is present in the same shell, it does not lose or gain energy.

6) When an electron obtains energy, it is excited to higher energy levels, and when it loses energy in the form of electromagnetic radiation, it is de-excited and returns to lower energy levels.


Excitation by Absorption of Light and De-Excitation by Emission of Light


Excitation by Absorption of Light and De-Excitation by Emission of Light


10.2 What does negative energy in the case of the hydrogen atom imply?

The energy of an electron in an atom is lower than the energy of a free electron at rest, as shown by the negative sign. The energy value of a free electron at rest is zero since it is infinitely far away from the nucleus (n = ). En becomes increasingly negative as the electron approaches closer to the nucleus (as n decreases). n=1 corresponds to the most stable orbit and has the largest negative energy value.


Note: Bohr’s model is applicable to H-atom or H-like species like He+,Li2+,Be3+ 


10.3 Transition of Electron

ΔE=Ef - Ei 

ΔE=[RHnf2][RHni2]

ΔE=RH[1ni21nf2]=2.18×1018[1ni21nf2]J/atom


The wavelength associated with the photon's absorption or emission is:


1λ = ΔEhc = RHhc[1ni21nf2]=1.09677×107[1ni21nf2]m1

Rydberg's formula is what it's called.


10.4 Line Spectrum of Hydrogen

The H2 molecules breakdown when an electric discharge is transmitted through gaseous hydrogen, and the energetically excited hydrogen atoms that result generate discrete frequency electromagnetic radiations. Several lines in the hydrogen spectra are named after their discoverer.


Because the energy of an electron cannot change continuously but can only have fixed values, we get discrete lines rather than a continuous spectrum. As a result, the energy of one electron can be quantified.


Line Spectrum of Hydrogen


Line spectrum of hydrogen


LYMAN Succession: When an electron jumps from one of the higher states to the ground state or first state (n = 1), a series of ultraviolet spectral lines is generated, which is known as the Lyman series.


As a result, according to Rydberg's formula, n1= 1, n2= 2,3,4,5...


BALMER Succession: When an electron goes from a higher state to a state with n=2, a series of spectral lines called the Balmer series is emitted in the visible range.


As a result, according to Rydberg's formula, n1= 2, n2= 3,4,5,6....


PASCHEN Succession: When an electron moves from one of the higher states to the n=3 state, a series of infrared spectral lines is generated, known as the Paschen series.


As a result, n1= 3 and n2= 4,5,6 in Rydberg's formula.


BRACKETT SERIES: When an electron moves from one of the higher states to the state with n = 4, it emits a series of infrared spectral lines known as the Brackett series.


As a result, according to Rydberg's formula, n1= 4, and n2= 5,6,7…


PFUND SERIES: When an electron goes from one of the higher states to the one with n = 4, it emits a series of infrared spectral lines known as the Pfund series. The formula of Rydberg is n1=5,6,7…


Ionization Energy: 10.5

It is the amount of energy necessary to totally remove an electron from an atom and turn it into a positive ion.


n1=1

n2=  


Limiting Line 10.6

It's the shortest wavelength line.i.e., n2= 


10.7 Limitations of Bohr’s Model

1) Inability to explain multi-electron atom line spectra.

2) It fails to account for the hydrogen spectra's finer characteristics (doublet-two closely spaced lines).

3) Inability to explain line splitting in the magnetic (Zeeman Effect) and electric (Stark Effect) fields- When a source generating radiation is placed in a magnetic or electric field, each spectral line splits up into a number of lines. The Zeeman Effect is the splitting of spectral lines in a magnetic field, while the Stark Effect is the splitting of spectral lines in an electric field.

4) It could not account for atoms' ability to form molecules through covalent connections.

5) He ignores matter's dual behaviour and contradicts the Heisenberg uncertainty principle.


11. QUANTUM MECHANICAL MODELING

This model was built around two ideas:

de Broglie, No. 1

(2) Heisenberg Uncertainty Principle (concept of dual nature of matter)

11.1 Matter's dual behaviour

According to de Broglie, matter should have dual behaviour, i.e. particle and wave-like qualities.

λ=hmv=hp=h2m(KE)=h2mq(V)


Where p denotes a particle's linear momentum.

Every moving item, according to de Broglie, has a wave character. Ordinary objects have wavelengths that are so short (due to their large masses) that their wave characteristics cannot be detected. Electrons and other subatomic particles (with very small masses) have wavelengths that can be measured experimentally.


11.2 Heisenberg's Principle of Uncertainty

It is impossible to measure the position and momentum of a tiny particle with exact precision at the same time. When one of these two parameters is measured with greater precision, the other becomes less precise. The product of positional uncertainty (x) and momentum uncertainty (p) is always a constant and is equal to or larger than h = 4π


(Δx).(Δp)h/4π

or (Δx).(mΔv)h/4π

or (Δx).(Δx)h/4πm


11.2.1 Explanation


Change of Momentum and Position of Electron on Impact with a Photon


Change of Momentum and Position of Electron on Impact with a Photon


Assume we're attempting to determine an electron's position as well as its momentum. We must utilise light to pin point the position of the electron, so that a photon of light strikes the electron and the reflected photon is seen in the microscope. The electron's location and velocity are both disrupted because of the collision.


11.2.2 The Importance of the Uncertainty Principle:

It eliminates the presence of distinct electron pathways or trajectories, as indicated in Bohr's Model.


12. ATOM QUANTUM MECHANICAL MODEL

Quantum mechanics is a theoretical science that studies the motion of small objects that have both particle and wave features. Schrodinger devised the fundamental equation of quantum mechanics.


The electron wave function ψ is described by this equation. This wave function retains all an electron's information, including its energy, location, and orbital. As a result, it has no physiologic relevance. Quantum Numbers can be used to obtain the information held in about an electron.


Probability: 12.1 The chance of detecting an electron at a given position within an atom is called density |ψ|2.


12.2 Orbital Concept

It's a three-dimensional area around the nucleus where the chances of finding an electron of a certain energy are highest (say upto 90 percent).


Quantum Numbers (12.3)

They can be characterised as a collection of four integers that provide complete information about all the electrons in an atom, such as their location, energy, the type of orbital they occupy, the shape and orientation of that orbital, and so on.


The Schrodinger wave equation yields three quantum numbers: Principal, Azimuthal, and Magnetic quantum numbers. Later, the Spin quantum number, the fourth quantum number, was postulated.


1) Quantum Principal Number (n):

It explains which shell an electron belongs to.

n = 1,2,3,4,5…

Based on electronic leaps between these shells, this number helps to describe the main lines of the spectrum.

(a) It offers the average distance between the nucleus and the electron. The distance from the nucleus increases as n increases.

(b) It determines the energy of a hydrogen atom or a hydrogen-like species fully.

Only the value of n determines the energy of an H-atom or H-like species.

Energy in ascending order: 1, 2, 3, 4, 5, and so on.

The energy of multi-electron species is determined by both the primary and azimuthal quantum numbers.

2n is the maximum number of electrons that can be found in any shell.


2) Azimuthal Quantum Number (l): Orbital Angular Momentum or Subsidiary Quantum Number. Because there are many sub-shells within a single shell, the number of electronic jumps increases, which explains the appearance of tiny lines in the spectrum. This quantum number indicates: 


(a) the number of subshells in a shell; 

(b) An electron's angular momentum in a subshell.

(c) The shapes of different subshells within the same shell.

(d) The relative energies of the different subshells.


Value of l varies from 0 to n – 1 For 1st shell (n = 1): l = 0 

2nd shell (n = 2): l = 0,1 

3rd shell (n = 3): l = 0,1,2 

4th shell (n = 4): l = 0,1,2,3


Value of I 

Designation of subsheII

0

s

1

p

2

d

3

f

4

g

5

h


The initial letters of the words sharp, principal, diffused, and fundamental are represented by the notations s,p,d,f. l = 4 is known as the g subshell, l = 5 is known as the h subshell, and so on.


Principal shell 

Subshells

1 st shell

l = 0 (s-subshell)

2 nd shell

l = 0,1 (s & p subshell)

3 rd shell

l = 0,1,2 (s,p & d subshell)

4 th shell

l = 0,1,2,3 (s,p,d & f subshell)


(3) Magnetic Quantum Number(m):

This quantum number is necessary to explain why, when a line spectrum source is placed in a magnetic field, each spectral line divides into several line segments (Zeeman effect).


Electrons in a subshell can arrange themselves in specific favoured regions of space around the nucleus termed orbitals under the influence of an external magnetic field.

The number of preferred electron orientations in a subshell is determined by the magnetic quantum number.


Because each orientation corresponds to an orbital, the number of orbitals present in any subshell is determined by the magnetic quantum number.


The value of m can be anything between – l and + l, including zero.


Sub-shell 

Orbitals(m)

Number of orbitals

s-subshell (l=0) 

m = 0

1

p-subshell (l=1)

m = -1, 0, 1

3

d-subshell (l=2)

m = –2, –1, 0, 1 ,2

5

f-subshell (l=3)

m = –3, –2, –1, 0, 1, 2, 3

7


Orbital 

Value of m

px

m = 0

py

m = + 1

pz

m = – 1


Orbital 

Value of m

dx2

m = 0

dxz

m = + 1

dyz

m = – 1

dx2 - y2

m = + 2

dxy

m = – 2


Degenerate orbitals are orbitals in the same subshell that have the same energy. Eg In the absence of a magnetic field, the three p-orbitals of a specific main shell have the same energy.


Similarly, the energy of all five d-subshell orbitals of a given shell is the same.


Thus, the sequence of energy for the H-atom is: 1s 2s = 2p 3s = 3p = 3d 4s = 4p = 4d = 4f…


The energy of the orbitals in multi electron atoms falls as the effective nuclear charge increases. Eg


E2s(H) > E2s(Li) > E2s(Na) > E2s(K)


Total number of orbitals in each shell = n2 


Total number of potential m values in each subshell = 2l + 1


4) Spin Quantum Number(s): An atom's electron spins around its own axis in addition to moving around the nucleus. Because an electron in an orbital can spin either clockwise or counterclockwise. As a result, s can only have two values.


 + 12or - 12

The magnetic characteristics of substances can be explained using this quantum number.


12.4 Shapes of atomic orbitals

(1) S-orbitals have the following shape:

(a) They are non-directional and spherically symmetric, which means that the probability of finding an electron at a given distance is equal in all directions.

(b) The 1s and 2s orbitals have the same shape, but the 2s orbital is larger.

(c) A node is a spherical shell within the 2s orbital where the electron density is zero.

(d) The value of the azimuthal quantum number (l) is zero (l=0), and the magnetic quantum number (m) can only have one value (m = 0).


Shape of S-orbital


Shape of S-orbital


(2) P-orbital shape: 

(a) It is made up of two lobes on either side of the plane that runs across the nucleus. The p-orbital is formed like a dumbbell.

(b) In p-orbitals, there are three distinct electron cloud orientations. As a result, the lobes of the p-orbital can be thought of as being along the x, y, and z axes. As a result, they are referred to as px, py, and pz. The three p-orbitals are arranged in a right-angle relationship.

(c) There are no p-orbitals in the first main energy level (Principal quantum number n = 1).

(d) Degenerate orbitals are the three p-orbitals of a given energy level that have the same energy in the absence of an external electric and magnetic field.

(e) P-orbitals, like s orbitals, grow as the energy of an atom's primary shell increases. As a result, the value of the azimuthal quantum number is one (l=1), but the magnetic quantum number has three values (m= –1, 0, and +1).


Shape of P-orbitals


Shape of P-orbitals


(3) D-orbitals' shapes:

(a) They are denoted by the letters dxy,dyz,dzx,and dx2y2. They resemble a four-leaf clover in appearance. The second d orbital, called dz2, resembles a doughnut.

(b) In the absence of a magnetic field, all five d orbitals have the same energy.

(c) =2 and magnetic quantum number values are –2, –1, 0, + 1,+ 2.

(d) There are no d orbitals in main shells 1 and 2.


Shape of D-orbitals


Shape of D-orbitals


We've drawn boundary surface diagrams, in which the surface of an orbital with a constant probability density psi 2 is drawn in space. It encloses the area where the chances of detecting the electron are extremely high. We don't construct a boundary surface map that encompasses a 100 percent likelihood of locating the electron since probability density has some value at any finite distance from the nucleus, no matter how small it is. As a result, drawing a boundary surface diagram of a hard size with a 100% likelihood of detecting the electron is impossible.


12.5 Nodes and nodal planes

Node: It's a region where there's no chance of anything happening.

There are two types of nodes: nodes that are connected to each other and nodes that are not connected


(1) Spherical or radial nodes: In an orbital, three-dimensional regions where the probability of locating the electron is zero.


n – – 1 = number of radial/ spherical nodes


Radial or Spherical Nodes in the Orbitals


Radial or Spherical Nodes in the Orbitals


(2) Planar or Angular Nodes: These are planes that cut through the nucleus and have no chance of locating an electron.


Nodes with Planar/Angular Shapes:

n - 1 is the total number of nodes.


Planar or Angular Nodes


Planar or Angular Nodes


12.6 Filling of orbitals in an atom

(1) The Aufbau Principle 

This principle states that in the ground state of an atom, the orbitals are filled in order of increasing energy. In other words, electrons occupy the lowest energy orbital initially and only enter higher energy orbitals once the lower energy orbitals have been filled.


Unlike the H-atom, where the energy of orbitals is solely determined by n, the energy of multi-electron orbitals is determined by both n and l. The (n+) rule can be used to calculate their energy ranking. The lower the value of (n+) for an orbital, the lower its energy, according to this rule. When two different types of orbitals have the same (n+) value, the orbital with the lower n value has less energy.


Aufbau Principle for Filling of Electron in the Orbitals


Aufbau Principle for Filling of Electron in the Orbitals


(2) Pauli Exclusion Principle: An orbital can only have two electrons, both of which must have the same spin.

Correct ↑↓ or ↓↑

 (i)                (ii)

Incorrect ↑↑ or ↓↓ 

 (iii)               (iv) 


(3) Hund's maximum multiplicity rule: Electron pairing in the p, d, and f orbitals can't happen until each subshell's orbital has one electron. All singly occupied orbitals will have parallel spin as well.


Atomic No. 

Element

Electronic Configuration

1

H

1s1

2

He

1s2

3

Li

[He]2s1

4

Be

[He] 2s2

5

B

[He] 2s2 2p1

6

C

[He] 2s2 2p2

7

N

[He] 2s2 2p3

8

O

[He] 2s2 2p4

9

F

[He] 2s2 2p5

10

Ne

[He] 2s2 2p6

11

Na

[Ne] 3s1

12

Mg

[Ne] 3s2

13

Al

[Ne] 3s23p1

14

Si

[Ne] 3s2 3p2

15

P

[Ne] 3s2 3p3

16

S

[Ne] 3s2 3p4

17

Cl

[Ne] 3s2 3p5

18

Ar

[Ne] 3s2 3p6

19

K

[Ar] 4s1

20

Ca

[Ar] 4s2

21

Sc

[Ar] 3d1 4s2

22

Ti

[Ar] 3d2 4s2

23

V

[Ar] 3d3 4s2

24

Cr

[Ar] 3d54s1

25

Mn

[Ar] 3d5 4s2

26

Fe

[Ar] 3d6 4s2

27

Co

[Ar] 3d7 4s2

28

Ni

[Ar] 3d8 4s2

29

Cu

[Ar] 3d10 4s1

30

Zn

[Ar] 3d10 4s2


12.7 Exceptional Configuration of Cr & Cu

Because of the following reasons, the filled and entirely half-filled subshells are stable:


1. Electron distribution that is symmetrical: It is widely known that symmetry promotes stability. Subshells that are totally filled or half- filled have a symmetrical distribution of electrons and are thus more stable. The energy of electrons in the same subshell (here 3d) is the same, but their spatial distribution is different. As a result, their mutual shielding is minimal, and the electrons are more strongly drawn to the nucleus.


2. Exchange Energy: When two or more electrons with the same spin are present in the degenerate orbitals of a subshell, the stabilising effect occurs. These electrons tend to swap locations, and the energy produced as a result of this swap is known as exchange energy. When the subshell is half-filled or totally filled, the maximum number of exchanges possible is reached. As a result, the exchange energy is at its highest, and the stability is at its best. Eg., Cr is [Ar] 3d54s1


Exchange of Energy by the Electrons in the Orbitals: 4 Exchanges by Elecrron 1; 3 Exchange by Electron 2


Exchange of Energy by the Electrons in the Orbitals: 4 Exchanges by Elecrron 1; 3 Exchange by Electron 2


Exchange of Energy by the Electrons in the Orbitals: 2 Exchanges by Electron 3; 1 Exchange by Electron 4


Exchange of Energy by the Electrons in the Orbitals: 2 Exchanges by Electron 3; 1 Exchange by Electron 4


As a result, the total number of exchanges is equal to ten.


12.8 Electronic Configuration of Ions

12.8.1 Cations are generated when an atom's outermost electrons are removed. We must remove the electrons from the highest main quantum number while removing the electrons.


Anions are produced when electrons are introduced to the innermost vacant shell of a molecule.


12.8.3 Magnetic moment: n(n + 2)B.M

B.Mis Bohr Magneton

The number of unpaired electrons is given by n.

The term paramagnetic refers to species having unpaired electrons, while diamagnetic refers to species with no unpaired electrons.


Rydberg equation: 1λ = RH[1n121n22]

RH = 109678cm - 1 and n2 > n1

c=λ×υ  and ν = 1λ

E = hv or hcλ


Bohr’s Model

En =  - 1312Z2n2kJ mol - 1

 =  - 2.178\times10 - 18Z2n2J/atom =  - 13.6Z2n2eV/atom


Velocity of electron, \upsilonn = 2.165 \times106Znm/s

Radius of orbit, 0.529n2Z{\AA}

Photoelectric effect h\nu  = hν0 + 12mν2

ν0= threshold frequency

de-Broglie equation: λ=hmv

Heisenberg’s uncertainty principle: \[{\Delta x \times \Delta p} \geqslant \dfrac{h}{4\pi }


14. MATHEMATICAL MODELLING OF BOHR’s POSTULATES

Consider an ion with an atomic number of (Z) and a single electron circling around its nucleus at a distance of 'r', as indicated in the diagram.


Bohr’s Atomic Model


Bohr’s Atomic Model


Charge on the nucleus =  + Ze

The electrostatic attraction (F) between the charge nucleus  + Ze and the electron (–e) is given by

F = K|q1||q2|r2

Where K = 14\pi ε0


K = 14\piε0

=9×109Nm2C2

F=K|Ze||e|r2=KZe2r2...(i)

The electron is subjected to centrifugal forces is mv2r...(ii)

This centrifugal force must be provided by the electrostatic force of attraction (F).

From (i) and (ii), we have :KZe2r2mv2r...(iii)

Electron angular momentum around the nucleus

mVr = nh2\pi ...(iv)

n is a positive integer

n = 1,2,3,...

solve (iii) and (iv)

V = 2\pi KZe2nh r = n2h24π2Kme2Z

Put K = 9 \times 109Nm2C - 2, e = 1.6 \times 10 - 19C and h = 6.63×1034

to get js in the above expressions

Velocity of an electron in nthorbit

Vn = 2.165 \times 106Znms - 1

Radius rn = 0.53n2Z{\AA}


The Total Energy of an electron in the nth orbit is now


K.E.n + E.P.E.n

T.E.n = 12mVn2 + K(Ze)( - e)r[E.P.E. = Kq1q2r]

T.E.n = 12(KZe2rn) + K(Ze)( - e)rn

EnT.En =  - KZe22rn


The Total Energy of an electron in the nth orbit is now


K.E.n = 12KZe2rn,P.E.n =  - KZe2rn and E.n=  - KZe22rn

K.E.n =  - E.n and  E.P.E.n= 2En

When we use the value of r n in the En expression, we get

En= - 2π2K2me4Z2n2h2


En= - 2.178×1019Z2n2J/atom

En= - 13.6Z2n2eV/atom


En= - 2.178×1019Z2n2J/atom

En= - 13.6Z2n2eV/atom

[leV = 1.6×1019J]

2.178×1018Z2n2×6.02×1023J/mole

 - 1312Z2n2kJ/mole


15. PROBABILITY DISTRIBUTION DIAGRAMS FOR 1s AND 2s


Probability Distribution Diagrams for 1s and 2s


Probability Distribution Diagrams for 1s and 2s


Class 11 Chemistry Chapter 2 Important Topics and Subtopics Covered 

Topic

Subtopics

1. Historical Models

  • Dalton's Atomic Theory

  • Thomson's Model

  • Rutherford's Model

  • Bohr's Model

2. Fundamental Particles

  • Protons

  • Neutrons

  • Electrons

  • Properties and Discovery

3. Atomic Number and Mass Number

  • Definition and Significance

  • Isotopes and Isobars

4. Quantum Mechanical Model

  • Wave-Particle Duality

  • Quantum Numbers: Principal, Azimuthal, Magnetic, Spin

  • Electron Configuration

5. Atomic Orbitals

  • s, p, d, and f Orbitals

  • Shapes and Types of Orbitals

  • Aufbau Principle, Pauli Exclusion Principle, Hund’s Rule


Class 11 Chemistry Chapters 2 Details, and Formulas and Concepts.

  1. de Broglie's Wavelength Equation:

    • \lambda = \frac{h}{mv}


  1. Heisenberg UNCERTainty Principle:

    • \Delta x \times \Delta p \geq \frac{h}{4\pi}

    • States that it is impossible to simultaneously determine the exact position and momentum of a particle.


  1. Quantum Numbers:

  • Principal Quantum Number (n): Describes the energy level of an electron in an atom.

  • Azimuthal Quantum Number (l): Describes the shape of the orbital.

  • Magnetic Quantum Number (m): Describes the orientation of the orbital in space. Spin Quantum Number (ms): Describes the spin of the electron.


  1. Aufbau Principle, Pauli's Exclusion Principle, and Hund's Rule:

    • Aufbau Principle: Electrons occupy the lowest energy orbitals available.

    • Pauli's Exclusion Principle: No two electrons in an atom can have the same set of four quantum numbers.

    • Hund's Rule: Electrons occupy orbitals singly before pairing up, and all electrons in singly occupied orbitals have the same spin.


Importance of Revision Notes for Class 11 Chemistry Chapter 2

  • Summarises Key Points: Condenses important concepts for quick review.

  • Saves Time: Provides a fast way to revise before exams.

  • Highlights Essentials: Focuses on crucial topics and definitions.

  • Improves Memory: Helps in better retention of information.   

  • Enhances Exam Prep: Targets weak areas for more effective study.

  • Clarifies Concepts: Simplifies complex ideas for easier understanding.

  • Includes Visuals: Uses diagrams and charts for better grasp.

  • Boosts Confidence: Prepares students thoroughly for exams.


Tips For Learning the Chemistry Class 11 Chapter 2

  1. Focus on core processes with illustrations and examples.

  2. Draw and label diagrams for clarity. 

  3. Create summaries of each process.

  4. Connect concepts to everyday examples.

  5. Solve past exam questions to test understanding.

  6. Explain concepts to others to reinforce learning.

  7. Revisit material frequently to retain information.

  8. Utilise platforms like Vedantu for additional support.


Conclusion

The Structure of Atom Chapter 2 in Class 11 Chemistry provides essential insights into the fundamental aspects of atomic theory and structure. It lays the groundwork for understanding more advanced chemical concepts and helps in grasping the principles of atomic behaviour and bonding. Mastery of these concepts is vital for progressing in chemistry and applying these principles to various chemical reactions and processes.


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FAQs on Structure of Atom Class 11 Notes: CBSE Chemistry Chapter 2

1. What are the key topics covered in the structure of atom Class 11 notes?

The key topics include historical atomic models, fundamental particles, atomic numbers, mass numbers, quantum mechanical models, and atomic orbitals.

2. What is included in the structure of atom notes?

The structure of atom notes covers atomic models, the discovery and properties of protons, neutrons, electrons, and quantum mechanical principles.

3. What does the structure of atom notes Class 11 cover?

The structure of atom notes Class 11 covers historical atomic models, properties of subatomic particles, quantum numbers, and atomic orbitals.

4. Where can I find the Class 11 chemistry structure of atom notes?

Class 11 chemistry structure of atom notes can be found on educational platforms like Vedantu.

5. What is the structure of atom short notes?

Structure of atom short notes concisely summarise the fundamental concepts related to atomic structure, including key models and principles.

6. How are the structure of atom Class 11 short notes useful?

Structure of atom Class 11 short notes are useful for quick revision and understanding of the core concepts before exams.

7. What is the focus of the structure of atom notes in Class 11?

The focus is on developing atomic theory, the nature of atomic particles, and the quantum mechanical aspects of atomic structure.

8. What are the main models of the atom discussed in Class 11 notes?

The main models include Dalton's Atomic Theory, Thomson's Model, Rutherford's Model, and Bohr's Model.

9. How are quantum numbers explained in the structure of atom notes?

Quantum numbers are explained in terms of their role in describing electron configurations and the shape and orientation of atomic orbitals.

10. Where can I download the structure of atom Class 11 notes PDF?

The structure of Atom Class 11 notes PDF can be downloaded from Vedantu, offering detailed and structured revision materials.