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Chemistry 11 Atomic Structure Notes

The document provides comprehensive notes on atomic structure, covering early atomic theories, the discovery and properties of electrons, protons, and neutrons, as well as Bohr's atomic theory and formulas for calculating the radius, energy, and frequency of electrons in orbits. It also includes self-assessment questions and tricks for solving related problems efficiently. Additionally, it discusses the limitations of Bohr's model in terms of its applicability and assumptions about electron behavior.

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0% found this document useful (0 votes)
43 views29 pages

Chemistry 11 Atomic Structure Notes

The document provides comprehensive notes on atomic structure, covering early atomic theories, the discovery and properties of electrons, protons, and neutrons, as well as Bohr's atomic theory and formulas for calculating the radius, energy, and frequency of electrons in orbits. It also includes self-assessment questions and tricks for solving related problems efficiently. Additionally, it discusses the limitations of Bohr's model in terms of its applicability and assumptions about electron behavior.

Uploaded by

shyhzadokhan12
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Chemistry 11 atomic structure notes

Summary of Key Points:


. Early Atomic Theory:
4
○ Greek philosophers Leucippus and Democritus (440 B.C) proposed
the concept of atoms as indivisible particles, laying the foundation for
atomic theory.
○ Most philosophers favored Aristotle's theory, which stated that matter
is composed of four elements: earth, water, air, and fire.
○ John Dalton (1803) introduced the modern atomic theory, marking a
significant shift in atomic understanding.
. Electrons:
○ Discovery: J.J. Thomson (1897) discovered the electron during
3
experiments with cathode rays.
○ Properties: Electrons have a negative charge, and their mass is about
1/1836th of a proton or neutron.
○ Location: Electrons revolve in orbits around the nucleus and occupy a
much larger volume than the nucleus but contribute less than 1% of
the atom's mass.
○ Role: Electrons determine atomic stability and chemical bonding, and
their arrangement in shells affects properties like boiling and melting
points.
. Protons:
○ Discovery: Discovered by Goldstein (1886) through experiments with
2
cathode rays.
○ Properties: Protons are positively charged and located in the nucleus.
They have the same magnitude of charge as electrons but a
significantly larger mass.
○ Role: The number of protons defines the atomic number of an
element, and protons and neutrons together make up the atomic
mass.
. Neutrons:
1
○ Discovery: James Chadwick (1932) discovered neutrons in an

experiment involving alpha particles and beryllium.
○ Properties: Neutrons are neutral particles (no charge), slightly heavier
than protons, and are found in the nucleus alongside protons.
○ Role: Neutrons contribute to the atom's mass but do not affect its
charge. They play a role in the stability of the nucleus and isotopes,
which have the same number of protons but different numbers of
neutrons.
. Properties of Subatomic Particles:
○ Electrons: Mass = 0.00055 amu, Charge = -1.602 × 10⁻¹⁹ Coulombs.
○ Protons: Mass = 1.0073 amu, Charge = +1.602 × 10⁻¹⁹ Coulombs.
○ Neutrons: Mass = 1.0086 amu, Charge = 0 (neutral), slightly heavier
than protons.

Self-Assessment Answers:
. Zn (Zinc):
○ Atomic number of Zn = 30 (so, it has 30 protons and 30 electrons).
○ The mass number of Zn is typically 65 (most abundant isotope).
○ Number of neutrons = Mass number - Atomic number = 65 - 30 = 35
neutrons.
. Mass Comparison (Electron vs Proton/Neutron):
○ The mass of an electron is approximately 1/1836th the mass of both a
proton and a neutron. Therefore, the mass of an electron is about
1836 times less than the mass of a proton or neutron.

Summary of Bohr's Atomic Theory:


. Bohr's Postulates:
○ Postulate 1: Electrons revolve in circular orbits at fixed distances from
the nucleus with a definite energy.
○ Postulate 2: An electron does not lose or gain energy as long as it
remains in the same orbit.
○ Postulate 3: When an electron jumps to a higher orbit (excitation), it
absorbs energy, and when it jumps to a lower orbit, it emits energy
(quantized).
○ Postulate 4: The angular momentum of the electron is quantized and
is an integral multiple of h/2pi here h is planks constant
1. Radius of n-th Orbit
Formula:
r = (a₀ × n²) / Z
where a₀ = 0.529 × 10⁻⁸ cm
Questions & Solutions:
. Find the radius of the second orbit (n=2) of a hydrogen atom (Z=1).
Solution:
r = (0.529 × 10⁻⁸ * 2²) / 1
r = (0.529 × 4) × 10⁻⁸
r = 2.116 × 10⁻⁸ cm
. What is the radius of the third orbit of a singly ionized helium atom (He⁺)
(Z=2)?
Solution:
r = (0.529 × 10⁻⁸ * 3²) / 2
r = (0.529 × 9) / 2 × 10⁻⁸
r = 2.38 × 10⁻⁸ cm
. If the radius of the first orbit of a hydrogen-like ion is 0.2645 × 10⁻⁸ cm, what
is its atomic number Z?
Solution:
0.2645 × 10⁻⁸ = (0.529 × 10⁻⁸ * 1²) / Z
Z = 0.529 / 0.2645
Z = 2 (Helium ion He⁺)
. Find the radius of the fourth orbit (n=4) of a Li²⁺ ion (Z=3).
Solution:
r = (0.529 × 10⁻⁸ * 4²) / 3
r = (0.529 × 16) / 3 × 10⁻⁸
r = 2.82 × 10⁻⁸ cm

2. Energy of Electron in n-th Orbit


Formula:
Eₙ = - K / n²
where K = 2.18 × 10⁻¹⁸ J/atom
Questions & Solutions:
. Calculate the energy of an electron in the first orbit (n=1) of a hydrogen
atom.
Solution:
E₁ = - (2.18 × 10⁻¹⁸) / 1²
E₁ = -2.18 × 10⁻¹⁸ J
. Find the energy of an electron in the third orbit (n=3) of a hydrogen atom.
Solution:
E₃ = - (2.18 × 10⁻¹⁸) / 3²
E₃ = -2.42 × 10⁻¹⁹ J
. An electron in a hydrogen-like ion has an energy of -5.45 × 10⁻¹⁹ J in its
.
second orbit. Identify the atomic number Z.
Solution:
Eₙ = - (K × Z²) / n²
-5.45 × 10⁻¹⁹ = - (2.18 × 10⁻¹⁸ * Z²) / 2²
Z² = (5.45 × 10⁻¹⁹ * 4) / 2.18 × 10⁻¹⁸
Z² = 4
Z = 2 (Helium ion He⁺)
. What is the energy of an electron in the fourth orbit of a hydrogen atom?
Solution:
E₄ = - (2.18 × 10⁻¹⁸) / 4²
E₄ = -1.36 × 10⁻¹⁹ J

3. Energy Difference Between Orbits


Formula:
ΔE = E₁ - E₂
Questions & Solutions:
. Find the energy difference when an electron jumps from n=3 to n=2 in
hydrogen.
Solution:
E₃ = -2.42 × 10⁻¹⁹ J
E₂ = -5.45 × 10⁻¹⁹ J
ΔE = (-5.45 + 2.42) × 10⁻¹⁹
ΔE = 3.03 × 10⁻¹⁹ J
. An electron moves from n=4 to n=2 in a hydrogen atom. Find the energy
difference.
Solution:
E₄ = -1.36 × 10⁻¹⁹ J
E₂ = -5.45 × 10⁻¹⁹ J
ΔE = (-5.45 + 1.36) × 10⁻¹⁹
ΔE = 4.09 × 10⁻¹⁹ J
. If an electron in a He⁺ ion jumps from n=3 to n=2, find the energy difference.
Solution:
For He⁺, Z=2, so K' = 4K.
ΔE = 1.21 × 10⁻¹⁸ J
. Find the energy difference when an electron moves from n=5 to n=3 in
hydrogen.
Solution:
ΔE = 1.55 × 10⁻¹⁹ J

4. Frequency of Photon Emitted


Formula:
ν = ΔE / h
where h = 6.626 × 10⁻³⁴ J·s
Questions & Solutions:
. Find the frequency of a photon emitted when an electron jumps from n=3 to
n=2 in hydrogen.
Solution:
ν = (3.03 × 10⁻¹⁹) / (6.626 × 10⁻³⁴)
ν = 4.57 × 10¹⁴ Hz
. What is the frequency of a photon for a transition from n=4 to n=2 in
hydrogen?
Solution:
ν = 6.17 × 10¹⁴ Hz
. Find the frequency of a photon emitted when an electron in He⁺ jumps from
n=3 to n=2.
Solution:
ν = 1.83 × 10¹⁵ Hz
. Calculate the frequency for a hydrogen electron transitioning from n=5 to
n=3.
Solution:
ν = 2.34 × 10¹⁴ Hz
Now I am solving these questions with tricks here are the tricks

1. Radius of n-th Orbit


Formula Trick:
r ∝ n² / Z
Shortcut: If you know the radius for one orbit, use:
r₂ = r₁ × (n₂² / n₁²) × (Z₁ / Z₂)
Solved Examples:
. Find the radius of the second orbit (n=2) of hydrogen (Z=1).
Trick: Multiply by (2²/1²).
r₂ = 0.529 × 4 = 2.116 × 10⁻⁸ cm
. Find the radius of the third orbit (n=3) of He⁺ (Z=2).
Trick: Use r₃ = r₁ × (3²/1²) × (1/2).
r₃ = (0.529 × 9) / 2 = 2.38 × 10⁻⁸ cm
. If r₁ = 0.2645 × 10⁻⁸ cm, find Z.
0.2645 = (0.529 × 1²) / Z
Z = 2 (Helium ion He⁺)
. Find the radius of the fourth orbit (n=4) of Li²⁺ (Z=3).
r₄ = (0.529 × 16) / 3 = 2.82 × 10⁻⁸ cm

2. Energy of Electron in n-th Orbit


Formula Trick:
Eₙ ∝ -Z² / n²
Shortcut: If you know energy for one level:
E₂ = E₁ × (n₁² / n₂²) × (Z₂² / Z₁²)
Solved Examples:
. Find the energy of the third orbit (n=3) of hydrogen.
Trick: E₁ = -13.6 eV.
E₃ = -13.6 / 3² = -1.51 eV
. Find energy of the second orbit (n=2) of He⁺ (Z=2).
Trick: Multiply by Z².
E₂ = -13.6 × 2² / 2² = -13.6 eV
. Energy of an electron in n=2 of a hydrogen-like ion is -5.45 eV. Find Z.
Trick: Use Eₙ = -13.6 × Z² / n²
-5.45 = -13.6 × Z² / 2²
Z² = 4 → Z = 2 (He⁺)
. Find energy in the fourth orbit (n=4) of hydrogen.
E₄ = -13.6 / 4² = -0.85 eV

3. Energy Difference (Photon Emitted)


Formula Trick:
ΔE = E₁ - E₂
Shortcut: Use Rydberg’s Formula:
ΔE = 13.6 × Z² × (1/n₁² - 1/n₂²)
Solved Examples:
. Find energy difference for transition from n=3 to n=2 in hydrogen.
Trick: Use ΔE = 13.6 × (1/2² - 1/3²).
ΔE = 13.6 × (1/4 - 1/9) = 1.89 eV
. Find energy difference for transition from n=4 to n=2 in hydrogen.
ΔE = 13.6 × (1/2² - 1/4²)
ΔE = 13.6 × (3/16) = 2.55 eV
. Find ΔE for an electron jumping from n=3 to n=2 in He⁺.
Trick: Multiply by Z².
ΔE = 13.6 × 4 × (5/36) = 3.78 eV
. Find energy difference for n=5 to n=3 in hydrogen.
ΔE = 13.6 × (1/3² - 1/5²)
ΔE = 1.55 eV

4. Frequency of Photon Emitted


Formula Trick:
ν = ΔE / h
h = 6.626 × 10⁻³⁴ J·s
Shortcut: Use:
ν = (3.29 × 10¹⁵ × Z²) × (1/n₁² - 1/n₂²)
Solved Examples:
. Find the frequency for transition from n=3 to n=2 in hydrogen.
Trick: Use ν = (3.29 × 10¹⁵) × (5/36).
ν = 4.57 × 10¹⁴ Hz
. Find frequency for transition from n=4 to n=2 in hydrogen.
ν = (3.29 × 10¹⁵) × (3/16)
ν = 6.17 × 10¹⁴ Hz
. Find frequency when an electron in He⁺ jumps from n=3 to n=2.
Trick: Multiply by Z².
ν = (3.29 × 10¹⁵ × 4) × (5/36)
ν = 1.83 × 10¹⁵ Hz
. Find frequency for transition from n=5 to n=3 in hydrogen.
ν = (3.29 × 10¹⁵) × (1/3² - 1/5²)
ν = 2.34 × 10¹⁴ Hz

Final Tricks for Quick Solving:


. Radius (r) → r ∝ n² / Z → Use ratios instead of full formula.
. Energy (E) → E ∝ -Z² / n² → Multiply known values by fractions.
. Energy Difference (ΔE) → Use Rydberg formula:
ΔE = 13.6 × Z² × (1/n₁² - 1/n₂²)
. Frequency (ν) → Use shortcut:
ν = (3.29 × 10¹⁵ × Z²) × (1/n₁² - 1/n₂²)

Bohr’s Atomic Model: Defects & Limitations


● Limited Applicability: Works only for hydrogen and single-electron species
(He⁺, Li²⁺, Be³⁺).
● Incorrect Orbital Shape: Assumes circular orbits, whereas electrons move
in 3D space.
● Violation of Uncertainty Principle: States electrons have a definite position
and velocity, contradicting Heisenberg's principle.
● No Wave Nature: Only explains the particle nature of electrons, ignoring
wave-like properties (de Broglie’s hypothesis).

Spectrum & Hydrogen Spectrum


Spectrum
● Monochromatic Light: Single wavelength (e.g., laser).
● Polychromatic Light: Multiple wavelengths (e.g., sunlight).
Types of Spectra
. Continuous Spectrum: Smooth transition of colors (e.g., rainbow).
. Line Spectrum: Distinct lines with dark spaces (fingerprint of elements).
Types of Line Spectrum
● Absorption Line Spectrum: Dark lines on bright background (light
absorbed).
● Emission Line Spectrum: Bright lines on dark background (light emitted).
Hydrogen Spectrum
● Electron absorbs energy → Moves to a higher energy level → Returns to a
lower level, emitting light.
● Series of Spectral Lines
○ Lyman (UV region): n₂ → n₁ (1st level).
○ Balmer (Visible region): n₂ → n₁ (2nd level).
○ Paschen (Near-IR region): n₂ → n₁ (3rd level).
○ Bracket (Mid-IR region): n₂ → n₁ (4th level).
○ Pfund (Far-IR region): n₂ → n₁ (5th level).

Planck’s Quantum Theory


● Energy is not emitted/absorbed continuously but in small packets called
quanta (photons).
● Higher frequency = Higher energy.

X-Rays
Discovery
● Discovered by W. Roentgen (1895) while working with cathode rays.
● High-energy electromagnetic waves that penetrate matter.
Types of X-Rays
● K-Series: Short wavelength, high energy (produced by heavy elements).
● L-Series: Long wavelength, low energy (produced by lighter elements).
Production
● Fast-moving electrons hit a metal anode → X-ray photons are emitted.
Properties
● Short wavelength (0.1–10 Å).
● Travel at the speed of light.
● High penetration power.
● Ionize gases and damage living cells.
Uses
● Medical imaging (fractures, dental issues).
● Cancer treatment.
● Baggage scanning at airports.
● Crystallography for structure determination.

Moseley’s Law & Atomic Number


● Moseley (1913) found that X-ray frequencies depend on the number of
protons in the nucleus.
● Moseley’s Law:

● Helped redefine the periodic table based on atomic number instead of


atomic mass.

Radioactivity
Discovery
● Henri Becquerel (1896) observed uranium emitting invisible radiation.
● Marie & Pierre Curie isolated radioactive elements Polonium & Radium.
Natural Radioactivity
Unstable nuclei spontaneously emit radiation until a stable element (Lead, Pb-82)
is formed.

Artificial Radioactivity
● Stable elements can be made radioactive by bombarding them with nuclear
particles.
Radiocarbon Dating
● Uses radioactive carbon-14 to determine the age of ancient objects
containing organic material.
Types of Radiation:
Rutherford’s Experiment:
● Alpha (α) rays: Deflected towards the south pole in the magnetic field,
composed of two protons and two neutrons, and have +2 charge. They have
the highest ionization power but the lowest penetration power. Their speed
is 1/10 to 1/20th of the speed of light.
● Beta (β) rays: Deflected towards the north pole in the magnetic field,
composed of electrons, with -1 charge. They have moderate ionization and
penetration power. Their speed is 9/10th of the speed of light.
● Gamma (γ) rays: No deflection in the electric or magnetic field, are
electromagnetic waves, and have the highest penetration power with zero
charge. They travel at the speed of light.
Comparison Table:

Property Alpha Rays Beta Rays Gamma Rays


Mass 4 amu 1/1836 amu Zero
Composition Helium Electron Electromag-
nucleus netic waves
Charge +2 -1 Neutral
Ionization High (100x β, Moderate Low
Power 10,000x γ)
Penetration Low Moderate High
Power
Speed 1/10 to 1/20 of 9/10 of light Speed of light
light speed speed
Uses of Nuclear Radiation:
. Medical Field:
○ Diagnosis, monitoring, and treatment of diseases (e.g., radiotherapy
for cancer).
○ Study of bone formation in mammals and nuclear medicine using
radioisotopes.
. Agriculture:
○ Treating seeds and producing new crop varieties using radioisotopes.
. Energy Production:
○ Nuclear power plants (e.g., Karachi Nuclear Power Plant) generate
electrical energy.
. Industries:
○ Quality control, density measurement of metals, and thickness
measurement of plastics.
. Geology:
○ Studying rocks and geological formations.
. Archaeology:
○ Carbon-14 isotope used for dating fossils and artifacts.

Quantum Numbers & Orbitals:


Quantum Numbers: These are integers that describe the energy levels, shapes,
and orientations of orbitals in atoms. There are four quantum numbers:
4:Spin Quantum Number (s):
○ Describes the spin of an electron.
○ Possible values: +1/2 (clockwise spin) or -1/2 (counter-clockwise
spin).
○ In the same orbital, two electrons cannot have the same spin quantum
number.
Summary of Quantum Numbers:

Energy Level Sub-level (l) Orientation Max


(n) (m) Electrons
1 0 1 2
2 0 1 2
2 1 -1, 0, +1 6
3 0 1 2
3 1 -1, 0, +1 6
3 2 -2, -1, 0, +1, 10
+2
4 0, 1, 2, 3 Various 14
Shapes of Orbitals:
. s-orbital:
○ Spherical shape, uniform probability of finding the electron.
○ One possible orientation in space.
○ No nodal planes.
○ Size increases with the increase in n.
. p-orbital:
○ Dumb-bell shape, oriented along the three axes (x, y, z).
○ Three degenerate p-orbitals (px, py, pz).
○ Each orbital has a nodal plane where the probability of finding the
electron is zero.
. d-orbital:
○ Five possible orientations in space (dxy, dyz, dxz, dx^2-y^2, dz²).
○ Complex

Electronic Configurations
The distribution of electrons in the available sub-shells (s, p, d, f) is called
electronic configuration.
● Superscripts: Indicate the number of electrons in the sub-shell.
● Coefficients: Indicate the shell number to which the sub-shell belongs.
Example: O = 1s² 2s² 2p⁴
● Electron Spin: Represented by an arrow.
○ Upward arrow (↑): Clockwise spin.
○ Downward arrow (↓): Anti-clockwise spin.

Rules for Electronic Configuration


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

numbers.
● The four quantum numbers are:
○ Principal quantum number (n)
○ Azimuthal quantum number (l)
○ Magnetic quantum number (m)
○ Spin quantum number (s)
● In a given orbital, two electrons must have opposite spins.
Example: In He (1s²), the first electron has clockwise spin (↑), the second
has anti-clockwise spin (↓).
2. Aufbau Principle
● Electrons fill orbitals in order of increasing energy, starting with the lowest
energy orbital (1s).
● Aufbau means "building-up," referring to how electrons progressively fill
sub-shells.
● Order of sub-shells in increasing energy:
1s < 2s < 2p < 3s < 3p < 4s < 3d < 4p < 5s < 4d < 5p < 6s < 4f
3. (n + l) Rule (Wiswesser Rule)
● Electrons fill orbitals in order of increasing (n + l) value.
○ If two orbitals have the same (n + l) value, the orbital with the lower n
is filled first.
● Example: 3d (n=3, l=2, n+l=5) vs. 4s (n=4, l=0, n+l=4) → 4s fills first
because it has a lower (n + l) value.

Isoelectronic Species
● Atoms or ions with the same number of electrons and the same electronic
configuration.
Example:
○ Ne (Z=10), Na⁺ (Z=10), and F⁻ (Z=10) all have the configuration 1s²
2s² 2p⁶.

Electronic Configurations of Elements


Example Configurations:
. S (Z = 16)
○ 1s² 2s² 2p⁶ 3s² 3p⁴
. Na⁺ (Z = 11)
○ 1s² 2s² 2p⁶
○ Note: Na⁺ has lost one electron, so it is isoelectronic with Ne.
. Cl (Z = 17)
○ 1s² 2s² 2p⁶ 3s² 3p⁶
○ Note: Cl has gained one electron, so it is isoelectronic with Ar.

Hund's Rule of Maximum Multiplicity


● In degenerate orbitals (orbitals with the same energy), electrons will be
placed in separate orbitals to maximize the number of unpaired electrons.
● Example: In filling p orbitals, 2px¹ 2py¹ 2pz¹ is preferred over 2px² 2py¹ 2pz⁰.
● More unpaired electrons = More stability.

Key Points for Filling Orbitals


. Energy Order:
○ Orbitals fill in the order of increasing energy: 1s < 2s < 2p < 3s < 3p <
4s < 3d < 4p
○ The (n + l) rule helps determine this filling order.
. Electron Spin:
○ Electrons in the same orbital must have opposite spins, as per Pauli's
Exclusion Principle.
. Orbital Energy:
○ For same (n + l) value, lower n fills first.

Self-Assessment: Identify Higher Energy Orbitals


Identify which orbital has higher energy in each pair:
. 4s vs. 3d → 3d
. 4f vs. 6p → 6p
. 5p vs. 6s → 5p
. 4s vs. 3d → 3d
Summary of Quantum Numbers:
● n (Principal Quantum Number): Defines the energy level.
● l (Azimuthal Quantum Number): Defines the sub-shell (s, p, d, f).
● m (Magnetic Quantum Number): Defines the orbital orientation.
● s (Spin Quantum Number): Defines the spin direction (↑ or ↓).

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