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Structure of Atom Class 11 Notes: Key Concepts, Formulas and Worked Examples

This complete structure of atom class 11 notes page is built for revision speed. It walks through the chapter in the order a teacher builds it: the discovery of electrons, protons and neutrons, the early atomic models, the wave–particle duality of radiation, Bohr’s model, and finally the quantum mechanical model with its four quantum numbers.

Every formula you need — Planck’s \( E = h\nu \), the Bohr energy and radius expressions, the de Broglie relation and Heisenberg’s uncertainty principle — is collected with symbol meanings and SI units.

Three numericals are solved step by step with fresh numbers, a common-mistakes table flags the traps that cost marks, and the quick revision summary gives you a one-page recap for the night before the exam.

Chapter Overview

This is a dense chapter that builds one idea on top of another. The table lists the topics in teaching order with the NCERT page ranges (Class 11 Chemistry Part I) so you know where each idea lives in the book.

# Topic NCERT pages What you will master
1 Discovery of sub-atomic particles 31–33 Charge, mass and discovery of electron, proton, neutron
2 Atomic models 33–37 Thomson plum pudding, Rutherford nuclear model, their drawbacks
3 Electromagnetic radiation + Planck’s quantum theory 38–43 Wave nature of light, \( c = \nu\lambda \), photoelectric effect, dual behaviour
4 Atomic spectra and Bohr’s model 44–50 Line spectra of hydrogen, Bohr’s postulates, energy and radius formulas
5 Towards quantum mechanics 50–54 de Broglie equation, Heisenberg uncertainty principle, Schrödinger equation
6 Quantum numbers and orbital shapes 55–59 \( n, l, m_l, m_s \); s, p, d orbital shapes; nodes

This chapter sits inside the Class 11 Chemistry notes, part of the Class 11 notes hub within the wider CBSE notes library. Before starting, make sure you own the mole and stoichiometry ideas in the Some Basic Concepts of Chemistry notes. The official chapter PDF is available from NCERT if you want the full diagrams alongside these notes.

Sub-Atomic Particles and Atomic Models

How electrons, protons and neutrons were discovered

Dalton’s 1808 atomic theory treated the atom as indivisible, but electrical discharge through gas-filled cathode ray tubes forced a revision (NCERT, p. 31).

  • Cathode rays start at the cathode and travel to the anode; they travel in straight lines and are deflected by electric and magnetic fields exactly like negatively charged particles.
  • Their behaviour is identical whatever the gas or electrode material, so electrons must be present in all atoms.
  • Thomson (1897) measured the charge-to-mass ratio: \( e/m_e = 1.758820 \times 10^{11}\ \text{C kg}^{-1} \).
  • Millikan’s oil drop experiment (1906–14) showed charge is quantised: \( q = ne \), with \( e = -1.602176 \times 10^{-19}\ \text{C} \).
  • Combining the two results gives the electron mass \( m_e = 9.1094 \times 10^{-31}\ \text{kg} \) (NCERT, p. 32).

The positive canal rays gave the proton — the lightest positive ion, obtained from hydrogen and characterised in 1919. Chadwick (1932) discovered the neutron by bombarding a thin sheet of beryllium with \( \alpha \)-particles (NCERT, p. 33).

Properties of the fundamental particles

Table 2.1 of the textbook collects the charge and mass data you must be able to quote.

Particle Symbol Absolute charge (C) Relative charge Mass (kg) Approx. mass (u)
Electron e \( -1.602176 \times 10^{-19} \) \( -1 \) \( 9.109382 \times 10^{-31} \) 0
Proton p \( +1.602176 \times 10^{-19} \) \( +1 \) \( 1.6726216 \times 10^{-27} \) 1
Neutron n 0 0 \( 1.674927 \times 10^{-27} \) 1

The proton and neutron have nearly equal mass, while the electron is far lighter. The neutron is slightly heavier than the proton. Protons and neutrons together are called nucleons (NCERT, p. 36).

Thomson’s plum pudding model

Thomson (1898) pictured the atom as a sphere of uniformly distributed positive charge (radius about \( 10^{-10}\ \text{m} \)) with electrons embedded in it — like plums in a pudding or seeds in a watermelon. The key assumption was that the mass of the atom is spread uniformly.

The model explained why the atom is electrically neutral, but it could not survive later experiments (NCERT, p. 34).

Rutherford’s nuclear model

Rutherford, with Geiger and Marsden, fired a stream of \( \alpha \)-particles at a thin gold foil about 100 nm thick, surrounded by a zinc sulphide screen (NCERT, p. 35). The three observations map to three conclusions:

Observation Conclusion
Most \( \alpha \)-particles passed straight through Most of the atom is empty space
A small fraction was deflected by small angles A concentrated positive charge repels them
About 1 in 20,000 bounced back (nearly 180°) The positive charge and nearly all mass sit in a tiny, dense nucleus

Rutherford’s model: a small positive nucleus (radius about \( 10^{-15}\ \text{m} \)) surrounded by electrons moving at high speed in circular orbits, held by electrostatic attraction. To grasp the scale: if the nucleus were a cricket ball, the atom’s radius would be about 5 km (NCERT, p. 35).

Atomic number, mass number, isotopes and isobars

  • Atomic number \( Z \) = number of protons in the nucleus = number of electrons in a neutral atom (NCERT, p. 36).
  • Mass number \( A \) = number of protons + number of neutrons.

Isotopes have the same atomic number but different mass numbers because they contain different numbers of neutrons — protium \( ^{1}\text{H} \), deuterium \( ^{2}\text{H} \), tritium \( ^{3}\text{H} \); \( ^{12}\text{C}, ^{13}\text{C}, ^{14}\text{C} \); \( ^{35}\text{Cl} \) and \( ^{37}\text{Cl} \). Isobars share the same mass number but differ in atomic number, for example \( ^{14}_{6}\text{C} \) and \( ^{14}_{7}\text{N} \).

All isotopes of an element show identical chemical behaviour, because chemistry is controlled by the electron count (NCERT, p. 36).

Why Rutherford’s model failed

Classical physics predicts that an accelerated charged particle radiates energy. An electron moving in a circular orbit is accelerating, so it should lose energy continuously and spiral into the nucleus in about \( 10^{-8}\ \text{s} \). Atoms are stable, so this cannot be right.

The model also said nothing about how electrons are distributed around the nucleus or what their energies are (NCERT, p. 37).

Thomson vs Rutherford vs Bohr: a comparison you must know

These three models form one of the most-tested threads of the chapter. Learn the contrast as one unit.

Feature Thomson model Rutherford model Bohr model
Positive charge Uniformly spread sphere Concentrated in a tiny nucleus Concentrated in a tiny nucleus
Electrons Embedded like plums Revolving in circular orbits Fixed circular orbits (stationary states)
Explains Electrical neutrality of the atom Scattering results, nuclear structure Stability and the line spectrum of hydrogen
Limitations Fails against scattering results Cannot explain stability (spiralling electron) No fine structure, fails for multi-electron atoms, no Zeeman/Stark effect

Electromagnetic Radiation and Quantum Theory

Wave nature of light

Maxwell showed that an accelerating charged particle generates alternating electric and magnetic fields that travel as electromagnetic waves. The two fields are perpendicular to each other and to the direction of travel. Electromagnetic waves need no medium and move in vacuum at \( c = 3.0 \times 10^{8}\ \text{m s}^{-1} \) (NCERT, p. 38–39).

\[ c = \nu \lambda \]

Frequency \( \nu \) (hertz, Hz = \( \text{s}^{-1} \)) is the number of waves passing a point in one second. Wavelength \( \lambda \) has units of length, with smaller units in common use: 1 Å = \( 10^{-10}\ \text{m} \), 1 nm = \( 10^{-9}\ \text{m} \). The wavenumber \( \bar{\nu} = 1/\lambda \) counts wavelengths per unit length, usually in \( \text{cm}^{-1} \) (NCERT, p. 39).

The electromagnetic spectrum, by frequency: radio (\( 10^6\) Hz, broadcasting), microwave (\( 10^{10}\) Hz, radar), infrared (\( 10^{13}\) Hz, heating), visible (\( 10^{15}\) Hz), ultraviolet (\( 10^{16}\) Hz). Visible light is only the tiny slice our eyes can detect (NCERT, p. 39).

Planck’s quantum theory — the staircase analogy

Classical physics could not explain black-body radiation, the photoelectric effect, the variation of heat capacity with temperature, or line spectra (NCERT, p. 40). In 1900 Planck proposed that energy is emitted or absorbed in discrete packets called quanta:

\[ E = h\nu \]

with Planck’s constant \( h = 6.626 \times 10^{-34}\ \text{J s} \). The allowed energies are \( E = 0, h\nu, 2h\nu, 3h\nu \dots \) — nothing in between (NCERT, p. 41). The staircase captures the idea: you can stand on any step of a staircase but never between two steps, so an oscillator can hold only whole multiples of \( h\nu \).

Photoelectric effect and Einstein’s equation

Hertz (1887) found that light can eject electrons from a metal surface. The key results (NCERT, p. 42):

  • Ejection is instantaneous — no time lag between light striking the metal and electrons leaving it.
  • The number of electrons ejected is proportional to the intensity (brightness) of light.
  • Each metal has a characteristic minimum threshold frequency \( \nu_0 \); below it no electrons come out, no matter how bright the light. Red light on potassium for hours ejects nothing, but weak yellow light works at once (\( \nu_0 \) for K = \( 5.0 \times 10^{14}\) Hz).
  • The kinetic energy of ejected electrons increases with frequency, not with intensity.

Einstein (1905) explained all of this by treating light as particles (photons). A photon of energy \( h\nu \) first supplies the work function \( W_0 = h\nu_0 \) to free the electron; the remainder becomes kinetic energy (NCERT, p. 43):

\[ h\nu = h\nu_0 + \tfrac{1}{2}m_e v^2 \]

Why this matters: intensity decides how many photons arrive, and therefore how many electrons are ejected; frequency decides each photon’s energy, and therefore the speed of each electron. Wave theory alone cannot explain why dim high-frequency light ejects electrons while bright low-frequency light does not.

Dual behaviour of radiation

Radiation shows wave properties (interference, diffraction) as it propagates, and particle properties when it interacts with matter. The two sides cannot be separated — light is both, depending on the experiment (NCERT, p. 43). Accepting this duality was the first step towards Bohr’s model and then quantum mechanics.

Atomic Spectra and Bohr’s Model

Emission, absorption and line spectra

A substance that has absorbed energy emits radiation at specific wavelengths — an emission spectrum. When white light passes through a sample, the wavelengths absorbed appear as dark lines — an absorption spectrum, the photographic negative of the emission spectrum.

Atoms in the gas phase give line spectra (bright lines with dark gaps), and each element’s line spectrum is unique, like a fingerprint used to identify it (NCERT, p. 45).

Hydrogen has the simplest spectrum. Balmer (1885) described its visible lines, and Rydberg generalised the result (NCERT, p. 46):

\[ \bar{\nu} = 109{,}677\left( \frac{1}{n_1^2} – \frac{1}{n_2^2} \right)\ \text{cm}^{-1} \]

The value \( 109{,}677\ \text{cm}^{-1} \) is the Rydberg constant for hydrogen. The series are named after their discoverers:

Series \( n_1 \) \( n_2 \) Spectral region
Lyman 1 2, 3, … Ultraviolet
Balmer 2 3, 4, … Visible
Paschen 3 4, 5, … Infrared
Brackett 4 5, 6, … Infrared
Pfund 5 6, 7, … Infrared

Bohr’s postulates (1913)

  1. The electron moves around the nucleus in fixed circular paths of fixed radius and energy, called orbits or stationary states, arranged concentrically.
  2. Energy in an orbit is constant; it changes only when the electron jumps between states, absorbing energy on the way up and emitting it on the way down.
  3. The frequency of radiation absorbed or emitted is given by Bohr’s frequency rule: \( \nu = \Delta E/h = (E_2 – E_1)/h \).
  4. Angular momentum is quantised: \( mvr = n(h/2\pi) \), where \( n = 1, 2, 3, \dots \) (NCERT, p. 47).

Energy and radius of hydrogen-like atoms

\[ E_n = -2.18 \times 10^{-18}\ \frac{Z^2}{n^2}\ \text{J} \qquad r_n = 52.9\ \frac{n^2}{Z}\ \text{pm} \]

For hydrogen (\( Z = 1 \)), the ground state (\( n = 1 \)) has energy \( E_1 = -2.18 \times 10^{-18}\ \text{J} \) and the first Bohr orbit radius is 52.9 pm (NCERT, p. 48). For a transition between levels (NCERT, p. 49):

\[ \Delta E = 2.18 \times 10^{-18}\left( \frac{1}{n_i^2} – \frac{1}{n_f^2} \right)\ \text{J} \]

Why the energy is negative: the zero of energy is assigned to an electron free from the nucleus — infinitely far away, \( n = \infty \). A bound electron has already released energy to stay near the nucleus, so its energy lies below zero. The most negative value (\( n = 1 \)) is the most stable, the ground state (NCERT, p. 48).

In emission the electron falls (\( n_f \lt n_i \)), so \( \Delta E \) is negative and energy is released; in absorption \( n_f \gt n_i \) and \( \Delta E \) is positive. The sign tells you the process.

Limitations of Bohr’s model

  • It cannot explain the fine structure of the hydrogen spectrum — doublet lines seen with high-resolution spectroscopy.
  • It fails for multi-electron atoms, even helium with only two electrons.
  • It cannot explain the splitting of spectral lines in a magnetic field (Zeeman effect) or an electric field (Stark effect).
  • It gives no picture of how atoms form molecules by chemical bonds (NCERT, p. 50).

At a deeper level, Bohr’s model treats the electron as a particle on a definite path, ignoring wave–particle duality and the uncertainty principle — precisely why it had to be replaced (NCERT, p. 53).

Quantum Mechanical Model and Quantum Numbers

de Broglie’s wave nature of matter

In 1924 de Broglie proposed that matter, like radiation, has wave character: every moving particle carries a wavelength (NCERT, p. 51):

\[ \lambda = \frac{h}{mv} = \frac{h}{p} \]

The prediction was confirmed when an electron beam was found to undergo diffraction. Ordinary objects have masses so large that their wavelengths are too short to measure — a 0.1 kg ball moving at 10 m s⁻¹ has \( \lambda \approx 6.626 \times 10^{-34}\ \text{m} \), far beyond any observable scale.

Practical application — the electron microscope: an ordinary microscope uses the wave nature of light, while an electron microscope uses the wave nature of fast electrons.

Because the electron’s wavelength is far shorter than light’s, the electron microscope reaches magnifications of about 15 million times and can resolve structures a light microscope cannot — a working use of de Broglie’s \( \lambda = h/mv \) (NCERT, p. 51).

Heisenberg’s uncertainty principle

Heisenberg (1927) stated that it is impossible to determine simultaneously the exact position and exact momentum (or velocity) of a particle (NCERT, p. 52):

\[ \Delta x \times \Delta p_x \geq \frac{h}{4\pi} \qquad \text{or} \qquad \Delta x \times m \Delta v \geq \frac{h}{4\pi} \]

The product of the two uncertainties is fixed: if position is known precisely (small \( \Delta x \)), velocity becomes very uncertain, and vice versa. To locate an electron you must illuminate it with photons of wavelength smaller than the electron, and that collision changes its momentum (NCERT, p. 52).

Significance: the principle rules out definite electron trajectories, and it matters only for microscopic objects. For a milligram-sized object \( \Delta v \cdot \Delta x \approx 10^{-28}\ \text{m}^2\ \text{s}^{-1} \), utterly negligible. For an electron \( \Delta v \cdot \Delta x \approx 10^{-4}\ \text{m}^2\ \text{s}^{-1} \): pin the position to \( 10^{-8}\ \text{m} \) and the velocity is uncertain by about \( 10^4\ \text{m s}^{-1} \).

A Bohr orbit cannot exist (NCERT, p. 53).

The quantum mechanical model

The Schrödinger equation \( \hat{H}\Psi = E\Psi \) gives quantised energy levels and the associated wave functions \( \Psi \). The wave function itself has no physical meaning; the probability density \( |\Psi|^2 \) gives the chance of finding the electron at a point.

An atomic orbital is the wave function of an electron in an atom, and no orbital can hold more than two electrons (NCERT, p. 54–55).

The four quantum numbers

Each orbital is labelled by three quantum numbers (\( n, l, m_l \)) that arise naturally from solving the Schrödinger equation; a fourth, \( m_s \), describes electron spin (NCERT, p. 55–56).

Quantum number Symbol Defines Allowed values
Principal \( n \) Size and (largely) energy of the orbital; identifies the shell \( n = 1, 2, 3, \dots \)
Azimuthal (orbital angular momentum) \( l \) Shape of the orbital; identifies the subshell \( l = 0 \) to \( (n-1) \)
Magnetic \( m_l \) Spatial orientation of the orbital \( -l \dots 0 \dots +l \) (\( 2l+1 \) values)
Spin \( m_s \) Orientation of the electron’s spin \( +\tfrac{1}{2} \) or \( -\tfrac{1}{2} \)

Subshell notation: \( l = 0, 1, 2, 3 \) correspond to s, p, d, f. Each subshell has \( 2l+1 \) orbitals: one s, three p, five d, seven f. The total number of orbitals in a shell is \( n^2 \) (NCERT, p. 56).

Orbit vs orbital — the distinction that marks many answers

An orbit is Bohr’s circular path of fixed radius; it has no real meaning because a definite path would violate the uncertainty principle. An orbital is a quantum mechanical region around the nucleus where the probability of finding the electron is high, described by \( |\Psi|^2 \) (NCERT, p. 57). This contrast is asked repeatedly — see the common mistakes table below.

Shapes of orbitals and nodes

  • s orbitals are spherical and spherically symmetric; size grows with \( n \) (\( 4s \) > \( 3s \) > \( 2s \) > \( 1s \)) (NCERT, p. 58).
  • p orbitals have two lobes (dumbbell shape) on either side of the nucleus; the three p orbitals (\( 2p_x, 2p_y, 2p_z \)) are mutually perpendicular and identical in energy (NCERT, p. 59).
  • d orbitals number five (\( d_{xy}, d_{yz}, d_{xz}, d_{x^2-y^2}, d_{z^2} \)); the first four are cloverleaf-shaped and similar, \( d_{z^2} \) differs, and all five are equal in energy (NCERT, p. 59).

Nodes are regions where the probability density is zero. Total nodes = \( n-1 \), made of \( l \) angular nodes plus \( (n-l-1) \) radial nodes (NCERT, p. 59).

Key Terms and Definitions

Revise these definitions in your own words; exams reward the precise term, not a vague description.

Term Meaning Example / formula
Cathode rays Stream of electrons moving from cathode to anode in a low-pressure discharge tube Deflected by electric and magnetic fields
Electron Negatively charged fundamental particle in all atoms \( e = -1.602176 \times 10^{-19}\ \text{C} \)
Proton Positively charged particle in the nucleus \( p = +1.602176 \times 10^{-19}\ \text{C} \)
Neutron Electrically neutral nuclear particle discovered by Chadwick Mass ≈ 1 u, slightly heavier than proton
Atomic number \( Z \) Number of protons in the nucleus Equals electron count in a neutral atom
Mass number \( A \) Total number of nucleons (protons + neutrons) \( A = Z + n \)
Nucleons Collective name for protons and neutrons Reside in the nucleus
Isotopes Same atomic number, different mass number \( ^{12}\text{C}, ^{13}\text{C}, ^{14}\text{C} \)
Isobars Same mass number, different atomic number \( ^{14}_6\text{C} \) and \( ^{14}_7\text{N} \)
Electromagnetic radiation Oscillating electric and magnetic fields travelling as waves Speed \( c = 3.0 \times 10^8\ \text{m s}^{-1} \) in vacuum
Wavelength \( \lambda \) Distance between successive wave crests SI unit: metre
Frequency \( \nu \) Number of waves passing a point per second Unit: Hz (\( \text{s}^{-1} \))
Wavenumber \( \bar{\nu} \) Number of wavelengths per unit length \( \bar{\nu} = 1/\lambda \) in \( \text{cm}^{-1} \)
Quantum Smallest amount of energy emitted or absorbed as radiation \( E = h\nu \)
Threshold frequency \( \nu_0 \) Minimum frequency that ejects an electron from a metal Below \( \nu_0 \), no photoelectric effect
Work function \( W_0 \) Minimum energy needed to remove an electron \( W_0 = h\nu_0 \)
Emission spectrum Bright lines at wavelengths an excited sample emits Unique for each element
Absorption spectrum Dark lines where a sample has absorbed light Negative of emission spectrum
Orbit Bohr’s fixed circular path of the electron No real physical meaning
Orbital Probability region around the nucleus described by \( |\Psi|^2 \) Holds at most two electrons
Node Region where probability density is zero Total nodes = \( n-1 \)

Formulas You Must Remember

Learn each formula with its symbols and units, then practise substituting values with units — that is what numerical questions actually test.

Formula Symbols and units Used for
\( c = \nu\lambda \) \( c \) = speed of light (\( 3.0 \times 10^8\ \text{m s}^{-1} \)); \( \nu \) in Hz; \( \lambda \) in m Converting between frequency and wavelength
\( \bar{\nu} = 1/\lambda \) \( \bar{\nu} \) in \( \text{m}^{-1} \) or \( \text{cm}^{-1} \) Spectroscopy, Rydberg formula
\( E = h\nu \) \( h = 6.626 \times 10^{-34}\ \text{J s} \); \( E \) in J Planck’s quantum theory, photon energy
\( h\nu = h\nu_0 + \tfrac{1}{2}m_e v^2 \) \( m_e \) = electron mass (kg); \( v \) = photoelectron speed (m s⁻¹) Photoelectric effect (Einstein)
\( E_n = -2.18 \times 10^{-18}\ (Z^2/n^2)\ \text{J} \) \( Z \) = atomic number; \( n \) = principal quantum number Bohr energy of hydrogen-like atoms
\( r_n = 52.9\ (n^2/Z)\ \text{pm} \) \( r_n \) in pm Bohr orbit radius
\( \Delta E = 2.18 \times 10^{-18}\ (1/n_i^2 – 1/n_f^2)\ \text{J} \) \( n_i \) = initial, \( n_f \) = final level Energy of a spectral transition
\( \nu = \Delta E/h \) \( \nu \) in Hz Bohr’s frequency rule
\( \lambda = h/mv \) \( m \) in kg; \( v \) in \( \text{m s}^{-1} \); \( \lambda \) in m de Broglie wavelength of a particle
\( \Delta x \cdot \Delta p_x \geq h/4\pi \) \( \Delta x \) in m; \( \Delta p_x \) in \( \text{kg m s}^{-1} \) Heisenberg uncertainty principle

Unit conversions to have ready: 1 Å = \( 10^{-10}\) m, 1 nm = \( 10^{-9}\) m, 1 pm = \( 10^{-12}\) m, 1 Hz = 1 s⁻¹. Always convert Å and nm to metres before substituting into formulas with \( h \) in J s.

Worked Examples with Original Numbers

These numericals use fresh numbers so you can practise picking the right formula, substituting with units, and quoting the answer with units — the exact skill exams test.

Example 1: Photon energy, frequency and wavelength for a hydrogen transition (n = 4 → n = 2)

Method: Use the Bohr energy-difference formula, then convert energy to frequency and wavelength.

Step 1: Write the transition with the correct sign.

For emission the electron falls from \( n_i = 4 \) to \( n_f = 2 \).

\[ \Delta E = 2.18 \times 10^{-18}\left( \frac{1}{n_i^2} – \frac{1}{n_f^2} \right)\ \text{J} = 2.18 \times 10^{-18}\left( \frac{1}{4^2} – \frac{1}{2^2} \right)\ \text{J} \]

Step 2: Simplify the bracket.

\[ \frac{1}{16} – \frac{1}{4} = \frac{1-4}{16} = \frac{-3}{16} \]

\[ \Delta E = 2.18 \times 10^{-18} \times \left( -\frac{3}{16} \right) = -4.09 \times 10^{-19}\ \text{J} \]

Step 3: The negative sign confirms emission — energy is released.

Use its magnitude for frequency.

\[ \nu = \frac{|\Delta E|}{h} = \frac{4.09 \times 10^{-19}}{6.626 \times 10^{-34}}\ \text{s}^{-1} = 6.17 \times 10^{14}\ \text{Hz} \]

Step 4: Convert frequency to wavelength using \( c = \nu\lambda \).

\[ \lambda = \frac{c}{\nu} = \frac{3.0 \times 10^8}{6.17 \times 10^{14}}\ \text{m} = 4.86 \times 10^{-7}\ \text{m} = 486\ \text{nm} \]

Final answer: A photon of energy \( 4.09 \times 10^{-19}\ \) J, frequency \( 6.17 \times 10^{14}\) Hz and wavelength 486 nm (blue-green, visible region) is emitted.

Example 2: de Broglie wavelength of an electron moving at 2.5 × 10⁶ m s⁻¹

Method: Apply \( \lambda = h/mv \) directly with mass in kg, velocity in \( \text{m s}^{-1} \), \( h \) in J s.

Step 1: Write the relation in symbols.

\[ \lambda = \frac{h}{mv} = \frac{6.626 \times 10^{-34}}{(9.11 \times 10^{-31})(2.5 \times 10^6)}\ \text{m} \]

Step 2: Multiply the denominator first.

\[ mv = 9.11 \times 10^{-31} \times 2.5 \times 10^6 = 2.28 \times 10^{-24}\ \text{kg m s}^{-1} \]

Step 3: Divide.

\[ \lambda = \frac{6.626 \times 10^{-34}}{2.28 \times 10^{-24}} = 2.91 \times 10^{-10}\ \text{m} = 0.291\ \text{nm} \]

Final answer: The electron has a de Broglie wavelength of \( 2.91 \times 10^{-10}\) m (about 291 pm).

Example 3: Minimum uncertainty in velocity of an electron confined to 0.15 nm

Method: Rearrange Heisenberg’s relation to solve for \( \Delta v \).

Step 1: Write the principle and convert \( \Delta x \) to metres.

\[ \Delta x \cdot m \Delta v \geq \frac{h}{4\pi} \quad\Rightarrow\quad \Delta v \geq \frac{h}{4\pi m \Delta x} \]

\[ \Delta x = 0.15\ \text{nm} = 1.5 \times 10^{-10}\ \text{m} \]

Step 2: Substitute values.

\[ \Delta v = \frac{6.626 \times 10^{-34}}{4 \times 3.14 \times (9.11 \times 10^{-31})(1.5 \times 10^{-10})}\ \text{m s}^{-1} \]

Step 3: Work out the denominator first.

\[ 4 \times 3.14 \times 9.11 \times 10^{-31} \times 1.5 \times 10^{-10} = 1.72 \times 10^{-39} \]

Step 4: Divide.

\[ \Delta v = \frac{6.626 \times 10^{-34}}{1.72 \times 10^{-39}} = 3.86 \times 10^5\ \text{m s}^{-1} \]

Final answer: The minimum uncertainty in the electron’s velocity is about \( 3.86 \times 10^5\) m s⁻¹ — so large that a definite trajectory (Bohr orbit) is impossible.

Common Mistakes to Avoid

The errors below are the ones that repeatedly cost students marks in this chapter. Learn each as an error → correction pair.

Mistake Correct rule How to check your answer
Writing “orbit” when the question means “orbital” An orbit is Bohr’s fixed circular path (no real meaning); an orbital is a probability region described by \( |\Psi|^2 \) Ask: does this electron follow a fixed path? If yes, it is an orbit — the modern model has no orbits
Dropping the negative sign in Bohr energy \( E_n \) is negative because a bound electron has lower energy than a free electron at zero; more negative = more stable Substitute \( n = 1 \) and \( n = \infty \); you must get \( -2.18 \times 10^{-18}\) J and 0
Wrong sign of \( \Delta E \) in emission vs absorption Emission (electron falls): \( \Delta E \) negative; absorption (electron rises): \( \Delta E \) positive Write \( n_f \gt n_i \) for absorption and check the bracket sign
Applying de Broglie to a macroscopic ball and expecting a measurable wavelength Large mass → wavelength far too short to detect; the relation holds, the effect is negligible Compare with atomic scale: a 0.1 kg ball gives about \( 10^{-34}\) m
Substituting \( \lambda \) in Å or nm without converting Convert first: 1 Å = \( 10^{-10}\) m, 1 nm = \( 10^{-9}\) m Check units cancel: J s ÷ (kg × m s⁻¹) must give metres
Using energy that depends only on \( n \) for multi-electron atoms For hydrogen and hydrogen-like ions energy depends only on \( n \); for multi-electron atoms it depends on both \( n \) and \( l \) If there is more than one electron, include \( l \) in energy ordering (\( 4s \) fills before \( 3d \))
Treating photoelectron kinetic energy as negative Energy is a scalar; the kinetic term \( \tfrac{1}{2}m_e v^2 \) is always positive, found from \( h\nu – h\nu_0 \) Subtract the work function from the photon energy; the remainder is positive

Exam Notes: Where Marks Are Won

  • Sub-atomic particles: quote charge and mass values to the precision given in Table 2.1, and name the scientist behind each discovery.
  • Rutherford’s experiment: give the three observations and pair each with its conclusion — one mark per correct pairing.
  • Photoelectric effect: define threshold frequency and work function precisely, write Einstein’s equation, and state that ejection is instantaneous.
  • Bohr model: be ready to write the energy and radius formulas, explain the negative sign, and state the angular momentum quantisation \( mvr = nh/2\pi \).
  • de Broglie and Heisenberg: give the formula, then one line on why each matters only for microscopic particles.
  • Quantum numbers: give allowed values for each, name what each defines, and know orbital shapes and nodes.
  • Numerical technique: write the formula first, substitute with units, show every step, and give the final answer with units — the substituted step earns the marks, not just the answer.

Vague definitions lose marks. For example, saying “the minimum light needed to eject electrons” without the words threshold frequency misses the mark — the exact term is part of the required answer.

Structure of Atom Class 11 Notes: Quick Revision Summary

Everything above, compressed to the ideas you must recall fast.

  • Particles: electron (negative, \( 9.1094 \times 10^{-31}\) kg), proton (positive, ≈ 1 u), neutron (neutral, ≈ 1 u).
  • Atomic models: Thomson (plum pudding) → Rutherford (nuclear, solar-system) → Bohr (quantised orbits) → quantum mechanical (orbitals, probability).
  • Radiation: \( c = \nu\lambda \), wavenumber \( 1/\lambda \); wave–particle duality.
  • Planck: energy in quanta, \( E = h\nu \), staircase analogy.
  • Photoelectric: \( h\nu = h\nu_0 + \tfrac{1}{2}m_e v^2 \); threshold frequency, work function.
  • Bohr: \( E_n = -2.18 \times 10^{-18}(Z^2/n^2)\) J, \( r_n = 52.9(n^2/Z)\) pm, \( \Delta E = 2.18 \times 10^{-18}(1/n_i^2 – 1/n_f^2)\) J.
  • de Broglie: \( \lambda = h/mv \) — basis of the electron microscope.
  • Heisenberg: \( \Delta x \cdot \Delta p_x \geq h/4\pi \) — rules out orbits for electrons.
  • Quantum numbers: \( n \) (size, shell), \( l \) (shape, subshell), \( m_l \) (orientation), \( m_s \) (spin).
  • Orbitals: s spherical, p dumbbell, d cloverleaf (and \( d_{z^2} \)); nodes = \( n-1 \).

Quantum numbers at a glance

Quantum number Defines Allowed values Orbitals contributed
\( n \) (principal) Size and energy, shell \( 1, 2, 3, \dots \) \( n^2 \) per shell
\( l \) (azimuthal) Shape, subshell \( 0 \) to \( (n-1) \) \( 2l+1 \) per subshell
\( m_l \) (magnetic) Orientation \( -l \dots 0 \dots +l \) one per value
\( m_s \) (spin) Spin direction \( +\tfrac{1}{2} \) or \( -\tfrac{1}{2} \) two electrons per orbital

Memory device: “Never Let Many Students Spin” — n gives Size, l gives Shape, m gives Orientation, s gives Spin.

Frequently Asked Questions

What is the difference between an orbit and an orbital?

An orbit is Bohr’s fixed circular path of the electron — a definite trajectory that the Heisenberg uncertainty principle makes impossible. An orbital is a quantum mechanical region around the nucleus where the probability of finding the electron is high, given by \( |\Psi|^2 \). An orbit has no real meaning; the orbital is the modern picture (NCERT, p. 57).

Why is the energy of an electron in a hydrogen atom negative?

Zero energy is assigned to an electron infinitely far from the nucleus (\( n = \infty \)). A bound electron has already released energy to stay near the nucleus, so its energy lies below zero. The most negative value (\( n = 1 \)) is the most stable — the ground state (NCERT, p. 48).

How does the photoelectric effect demonstrate the particle nature of light?

Light transfers energy instantly, in discrete packets (\( h\nu \)), when photons strike electrons — there is no time lag. The kinetic energy of ejected electrons depends on frequency, not intensity: dim high-frequency light ejects electrons while bright low-frequency light does not (below \( \nu_0 \)). Wave theory alone cannot explain either result (NCERT, p. 42–43).

Can the Heisenberg uncertainty principle be applied to a macroscopic object like a cricket ball?

The principle holds for everything, but for macroscopic masses the uncertainty product is negligible. For a milligram-sized object \( \Delta v \cdot \Delta x \approx 10^{-28}\ \text{m}^2\ \text{s}^{-1} \) — far too small to matter. It becomes significant only for microscopic particles like electrons (NCERT, p. 53).

What information does each quantum number give about an electron?

The principal quantum number \( n \) gives the size and largely the energy of the orbital and identifies the shell. The azimuthal quantum number \( l \) gives the shape and identifies the subshell.

The magnetic quantum number \( m_l \) gives the spatial orientation of the orbital, and the spin quantum number \( m_s \) gives the direction of electron spin (\( +\tfrac{1}{2} \) or \( -\tfrac{1}{2} \)) (NCERT, p. 55–57).

Reference: NCERT Class 11 Chemistry textbook, chapter 2 — Structure of Atom.

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