Light & Electronic Structure

General Chemistry I · Dr. Karmach

build Aug 09 · 11:09 · CC BY-NC-SA 4.0 · OpenStax Chemistry 2e where noted
Dr. Karmach

By the end of this unit, you can…

  • Relate a light wave's wavelength, frequency, and energy using c = λν and E = hν
  • Calculate the energy of a photon from its wavelength or frequency
  • State how many electrons each sublevel (s, p, d, f) holds and why
  • Write the ground-state electron configuration of an atom using the building-up order
  • Predict periodic trends in atomic radius, ionization energy, and electronegativity from an element's position
Dr. Karmach

Today's route 🗺️

  1. Wavelength & Frequency
  2. Photon Energy
  3. The Bohr Model & Line Spectra
  4. Quantum Numbers
  5. Orbital Shapes & Nodes
  6. Sublevels & Orbitals
  7. Electron Configurations
  8. Electron Configurations of Ions
  9. Exceptions — Chromium & Copper
  10. Periodic Trends
  11. Paramagnetism & Diamagnetism
Dr. Karmach

1 · Wavelength & Frequency

Use c = λν to find a wavelength or a frequency for any kind of light, converting nanometers to meters so the units match the speed of light.

Dr. Karmach

Every station, the same kind of wave

Turn the tuner across the dial and the station changes. Every one sends the same kind of radio wave. Only the number is different.

Dr. Karmach

One speed for all light

Light is an electromagnetic wave. In a vacuum, every kind travels at one speed, c = 3.00×10⁸ m/s. Stretch the wave and fewer crests pass each second; squeeze it and more do.

Dr. Karmach

The equation: c = λν

c = λ × ν
c = 3.00×10⁸ m/s · λ in meters (m) · ν in s⁻¹, also called hertz (Hz)

Wavelength λ is the distance from one crest to the next, in meters. Frequency ν is how many crests pass each second, in s⁻¹. Their product is always the fixed speed c.

Dr. Karmach

The electromagnetic spectrum

The same equation covers every kind of light, from radio waves meters long to gamma rays smaller than an atom. Visible light is a thin band: red near 700 nm, violet near 400 nm.

Dr. Karmach

The method

  1. Identify the unknown. λ or ν; the other two are given.
  2. Match units to c. Wavelength in meters, frequency in s⁻¹.
  3. Rearrange for the unknown: ν = c/λ, or λ = c/ν.
  4. Substitute and cancel units.
Dr. Karmach

Worked example 1 — frequency of orange light

c = λν
given: λ = 600 nm (orange) · c = 3.00×10⁸ m/s · wanted: ν

A lamp glows with orange light at 600 nm. Find its frequency. (c = 3.00×10⁸ m/s; 1 m = 10⁹ nm)

Identify the unknown, and match its units to c before dividing.

Dr. Karmach

Worked example 1 — solution

c = λν
given: λ = 600 nm (orange) · c = 3.00×10⁸ m/s · wanted: ν

Step 1 · Identify the unknown

c and λ are given; the frequency ν is the unknown.

Dr. Karmach

Worked example 1 — solution

c = λν
given: λ = 600 nm (orange) · c = 3.00×10⁸ m/s · wanted: ν
Step 1 · Identify the unknown Step 2 · Match units to c

c is meters per second, so put λ in meters: 600 nm × (1 m / 10⁹ nm) = 6.00×10⁻⁷ m.

Dr. Karmach

Worked example 1 — solution

c = λν
given: λ = 600 nm (orange) · c = 3.00×10⁸ m/s · wanted: ν
Step 1 · Identify the unknown Step 2 · Match units to c Step 3 · Rearrange for the unknown

ν = c/λ.

Dr. Karmach

Worked example 1 — solution

c = λν
given: λ = 600 nm (orange) · c = 3.00×10⁸ m/s · wanted: ν
Step 1 · Identify the unknown Step 2 · Match units to c Step 3 · Rearrange for the unknown Step 4 · Substitute and cancel units
ν = 3.00×10⁸ m/s6.00×10⁻⁷ m = 5.00×10¹⁴ s⁻¹
600 nm is orange light, and 5.00×10¹⁴ s⁻¹ lands in the middle of the visible range. ✓
Dr. Karmach

Worked example 2 — wavelength of a radio station

c = λν
given: ν = 100.0 MHz · c = 3.00×10⁸ m/s · wanted: λ

An FM station broadcasts at 100.0 MHz (1 MHz = 10⁶ s⁻¹). Find the wavelength of its radio wave. (c = 3.00×10⁸ m/s)

This time the frequency is given and the wavelength is unknown.

Dr. Karmach

Worked example 2 — solution

c = λν
given: ν = 100.0 MHz · c = 3.00×10⁸ m/s · wanted: λ

Step 1 · Identify the unknown

c and ν are given; the wavelength λ is the unknown.

Dr. Karmach

Worked example 2 — solution

c = λν
given: ν = 100.0 MHz · c = 3.00×10⁸ m/s · wanted: λ
Step 1 · Identify the unknown Step 2 · Match units to c

Put the frequency in s⁻¹: 100.0 MHz = 100.0 × 10⁶ s⁻¹ = 1.00×10⁸ s⁻¹.

Dr. Karmach

Worked example 2 — solution

c = λν
given: ν = 100.0 MHz · c = 3.00×10⁸ m/s · wanted: λ
Step 1 · Identify the unknown Step 2 · Match units to c Step 3 · Rearrange for the unknown

λ = c/ν.

Dr. Karmach

Worked example 2 — solution

c = λν
given: ν = 100.0 MHz · c = 3.00×10⁸ m/s · wanted: λ
Step 1 · Identify the unknown Step 2 · Match units to c Step 3 · Rearrange for the unknown Step 4 · Substitute and cancel units
λ = 3.00×10⁸ m·s⁻¹1.00×10⁸ s⁻¹ = 3.00 m
A 3-meter wave, far longer than any visible light. Long waves and low frequencies travel together, which is why these are called radio waves. ✓
Dr. Karmach

Your turn — frequency of green light

c = λν
given: λ = 500 nm (green) · c = 3.00×10⁸ m/s · wanted: ν

A leaf reflects green light near 500 nm. Convert it to meters, then divide c by it.

ν = cλ = 3.00×10⁸ m/s m = s⁻¹
Dr. Karmach

Your turn — frequency of green light

c = λν
given: λ = 500 nm (green) · c = 3.00×10⁸ m/s · wanted: ν

A leaf reflects green light near 500 nm. Convert it to meters, then divide c by it.

ν = cλ = 3.00×10⁸ m/s m = s⁻¹
ν = 3.00×10⁸ m/s5.00×10⁻⁷ m = 6.00×10¹⁴ s⁻¹
500 nm is green, between red and violet, and 6.00×10¹⁴ s⁻¹ falls right in the visible range. ✓
Dr. Karmach

Where this goes wrong

ν = c/λ
600 nm orange light · c = 3.00×10⁸ m/s · correct ν = 5.00×10¹⁴ s⁻¹
Leaving the wavelength in nanometers. 3.00×10⁸ ÷ 600 = 5.00×10⁵ s⁻¹, a factor of 10⁹ too small. c is meters per second, so λ must be in meters: 600 nm = 6.00×10⁻⁷ m.
Multiplying c by the wavelength. 3.00×10⁸ × 6.00×10⁻⁷ = 180. Its units are m²/s, not a frequency. Rearrange c = λν to ν = c/λ, with λ underneath.
Putting the speed of light on the bottom. λ ÷ c = 6.00×10⁻⁷ ÷ 3.00×10⁸ = 2.00×10⁻¹⁵ s, a time in seconds, not a frequency. Frequency needs c on top.
Dr. Karmach

Practice 1

c = λν
given: λ = 400 nm (violet) · c = 3.00×10⁸ m/s · wanted: ν

Violet light sits at 400 nm. What is its frequency? (c = 3.00×10⁸ m/s; 1 m = 10⁹ nm)

  1. 7.50×10⁵ s⁻¹
  2. 7.50×10¹⁴ s⁻¹
  3. 1.20×10² m²/s
  4. 1.33×10⁻¹⁵ s
Dr. Karmach

Practice 1 — answer: B

ν = c/λ
given: λ = 400 nm = 4.00×10⁻⁷ m · c = 3.00×10⁸ m/s
ν = 3.00×10⁸ m/s4.00×10⁻⁷ m = 7.50×10¹⁴ s⁻¹ — answer B

A left the wavelength in nanometers: 3.00×10⁸ ÷ 400 = 7.50×10⁵ s⁻¹, smaller by 10⁹. C multiplied c by λ: 3.00×10⁸ × 4.00×10⁻⁷ = 1.20×10², with units m²/s. D put c on the bottom: 4.00×10⁻⁷ ÷ 3.00×10⁸ = 1.33×10⁻¹⁵ s, a time.

400 nm is violet, the short-wavelength edge, so its frequency is the highest in the visible range. ✓
Dr. Karmach

Worked example 3 — frequency of ultraviolet light

c = λν
given: λ = 250 nm (ultraviolet) · c = 3.00×10⁸ m/s · wanted: ν

A sterilizing lamp emits ultraviolet light at 250 nm. Find its frequency. (c = 3.00×10⁸ m/s; 1 m = 10⁹ nm)

A common first attempt: divide c by 250 with no unit change. Test the result.

Dr. Karmach

Worked example 3 — solution

c = λν
given: λ = 250 nm (ultraviolet) · c = 3.00×10⁸ m/s · wanted: ν

A common first attempt

ν = 3.00×10⁸ m/s250 m = 1.20×10⁶ s⁻¹ ✗

That frequency belongs to radio waves, not ultraviolet light. The 250 went in as meters.

Dr. Karmach

Worked example 3 — solution

c = λν
given: λ = 250 nm (ultraviolet) · c = 3.00×10⁸ m/s · wanted: ν
A common first attempt
ν = 3.00×10⁸ m/s250 m = 1.20×10⁶ s⁻¹ ✗
Step 1 · Identify the unknown

c and λ are given; the frequency ν is the unknown.

Dr. Karmach

Worked example 3 — solution

c = λν
given: λ = 250 nm (ultraviolet) · c = 3.00×10⁸ m/s · wanted: ν
A common first attempt
ν = 3.00×10⁸ m/s250 m = 1.20×10⁶ s⁻¹ ✗
Step 1 · Identify the unknown Step 2 · Match units to c

c is meters per second, so λ must be in meters: 250 nm × (1 m / 10⁹ nm) = 2.50×10⁻⁷ m.

In meters the wavelength reads 2.50×10⁻⁷, smaller than the bare 250 by 10⁹. That missing factor is the whole error. ✓
Dr. Karmach

Worked example 3 — frequency

ν = c/λ
λ = 2.50×10⁻⁷ m (250 nm) · c = 3.00×10⁸ m/s · wanted: ν

Step 3 · Rearrange for the unknown

Solve for the unknown: ν = c/λ.

Dr. Karmach

Worked example 3 — frequency

ν = c/λ
λ = 2.50×10⁻⁷ m (250 nm) · c = 3.00×10⁸ m/s · wanted: ν
Step 3 · Rearrange for the unknown Step 4 · Substitute and cancel units
ν = 3.00×10⁸ m/s2.50×10⁻⁷ m = 1.20×10¹⁵ s⁻¹
Ultraviolet sits past violet, so its frequency runs higher than visible light. The unconverted route gave 1.20×10⁶ s⁻¹, a radio frequency for a UV lamp. ✗ vs ✓
Dr. Karmach

Take-home: convert to meters first

nm left as meters: ν = c ÷ 250 = 1.20×10⁶ s⁻¹
a radio frequency for UV light, off by 10⁹ ✗
converted: 250 nm = 2.50×10⁻⁷ m, then ν = c/λ = 1.20×10¹⁵ s⁻¹
λ in meters, so the meters in c cancel ✓

c is meters per second, so the wavelength must be in meters before it meets c. Convert nm to meters first. Skip it and the answer is off by a factor of 10⁹.

Dr. Karmach

Practice 2

c = λν
given: λ = 480 nm (blue) · c = 3.00×10⁸ m/s · wanted: ν

Blue light has a wavelength of 480 nm. What is its frequency? (c = 3.00×10⁸ m/s; 1 m = 10⁹ nm)

  1. 6.25×10⁵ s⁻¹
  2. 1.60×10⁻¹⁵ s
  3. 6.25×10¹⁴ s⁻¹
  4. 1.44×10² m²/s
Dr. Karmach

Practice 2 — answer: C

ν = c/λ
given: λ = 480 nm = 4.80×10⁻⁷ m · c = 3.00×10⁸ m/s
ν = 3.00×10⁸ m/s4.80×10⁻⁷ m = 6.25×10¹⁴ s⁻¹ — answer C

A left the wavelength in nanometers: 3.00×10⁸ ÷ 480 = 6.25×10⁵ s⁻¹, smaller by 10⁹. B put c on the bottom: 4.80×10⁻⁷ ÷ 3.00×10⁸ = 1.60×10⁻¹⁵ s, a time. D multiplied c by λ: 3.00×10⁸ × 4.80×10⁻⁷ = 1.44×10², with units m²/s.

480 nm is blue light, so its frequency lands in the visible range, just above green. ✓
Dr. Karmach

Check yourself

  1. Blue light has a wavelength of 450 nm. Solve c = λν for its frequency in symbols. Which unit cancels, and which one survives?
  2. A microwave oven runs at 2.45×10⁹ s⁻¹. Set up c = λν for its wavelength. Is that wave longer or shorter than visible light?

Frequency also fixes a photon's energy through E = h·ν, with h a constant. A higher frequency means more energy per photon, which is why ultraviolet light burns skin and radio waves pass through harmlessly.

Dr. Karmach

2 · Photon Energy

Find the energy of one photon from its frequency with E = hν, or from its wavelength with E = hc/λ, remembering that a shorter wavelength and a higher frequency both mean more energy per photon.

Dr. Karmach

Sunlight and sunscreen

Ultraviolet light burns skin. The visible light beside it does not. The difference is not brightness. Each packet of ultraviolet carries far more energy than a packet of visible light.

Dr. Karmach

Light comes in packets

Light arrives in discrete packets called photons. Each photon carries a fixed energy. A brighter beam sends more photons, not more energetic ones. Frequency sets each photon's energy.

Dr. Karmach

The photon energy formula

One photon's energy equals Planck's constant times the light's frequency. Planck's constant, h, is fixed at 6.626×10⁻³⁴ J·s. A higher frequency means a higher-energy photon.

Dr. Karmach

From wavelength: E = hc/λ

ν = c/λ → E = h · ν = h · c / λ
a wavelength gives a frequency, and a frequency gives an energy · convert nm to meters first

A light wave's frequency and wavelength are tied by ν = c/λ. Substitute that into E = hν to get a photon's energy straight from its wavelength.

Dr. Karmach

Shorter wavelength, more energy

Across the spectrum, wavelength shrinks and frequency climbs together, so the energy per photon climbs too. Radio photons are feeble. Ultraviolet photons carry enough energy to break bonds in skin.

Dr. Karmach

The method

  1. Identify the given and the unknown. Convert a wavelength to meters first.
  2. Choose the formula: E = hν from a frequency, E = hc/λ from a wavelength.
  3. Substitute and cancel units.
  4. Check the size: shorter wavelength, more energy.
Dr. Karmach

Worked example 1 — energy from a frequency

E = h · ν
given: ν = 5.00×10¹⁴ s⁻¹ · h = 6.626×10⁻³⁴ J·s · wanted: E

A photon of orange light has a frequency of 5.00×10¹⁴ s⁻¹. What is its energy? (h = 6.626×10⁻³⁴ J·s)

Identify the given and the unknown, then choose the formula.

Dr. Karmach

Worked example 1 — solution

E = h · ν
given: ν = 5.00×10¹⁴ s⁻¹ · h = 6.626×10⁻³⁴ J·s · wanted: E

Step 1 · Identify the given

ν = 5.00×10¹⁴ s⁻¹ is a frequency, already in s⁻¹. There is no wavelength to convert. The unknown is E.

Dr. Karmach

Worked example 1 — solution

E = h · ν
given: ν = 5.00×10¹⁴ s⁻¹ · h = 6.626×10⁻³⁴ J·s · wanted: E
Step 1 · Identify the given Step 2 · Choose the formula

A frequency is given, so E = hν gives the energy directly.

Dr. Karmach

Worked example 1 — solution

E = h · ν
given: ν = 5.00×10¹⁴ s⁻¹ · h = 6.626×10⁻³⁴ J·s · wanted: E
Step 1 · Identify the given Step 2 · Choose the formula Step 3 · Substitute and cancel units
E = 6.626×10⁻³⁴ J·s × 5.00×10¹⁴ s⁻¹ = 3.31×10⁻¹⁹ J

s and s⁻¹ cancel, leaving joules.

Dr. Karmach

Worked example 1 — solution

E = h · ν
given: ν = 5.00×10¹⁴ s⁻¹ · h = 6.626×10⁻³⁴ J·s · wanted: E
Step 1 · Identify the given Step 2 · Choose the formula Step 3 · Substitute and cancel units
E = 6.626×10⁻³⁴ J·s × 5.00×10¹⁴ s⁻¹ = 3.31×10⁻¹⁹ J
Step 4 · Check the size
One photon of visible light carries about 10⁻¹⁹ J. A single packet of light holds only a tiny amount of energy. ✓
Dr. Karmach

Worked example 2 — energy from a wavelength

E = h · c / λ
given: λ = 400 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E

A photon of violet light has a wavelength of 400 nm. What is its energy? (1 m = 10⁹ nm)

Convert the wavelength to meters, then substitute.

Dr. Karmach

Worked example 2 — solution

E = h · c / λ
given: λ = 400 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E

Step 1 · Identify the given

Convert the wavelength to meters so it matches c: 400 nm × (1 m / 10⁹ nm) = 400×10⁻⁹ m. The unknown is E.

Dr. Karmach

Worked example 2 — solution

E = h · c / λ
given: λ = 400 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E
Step 1 · Identify the given Step 2 · Choose the formula

A wavelength is given. Frequency and wavelength are tied by ν = c/λ, so E = hν becomes E = hc/λ.

Dr. Karmach

Worked example 2 — solution

E = h · c / λ
given: λ = 400 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E
Step 1 · Identify the given Step 2 · Choose the formula Step 3 · Substitute and cancel units
E = 6.626×10⁻³⁴ J·s × 3.00×10⁸ m/s400×10⁻⁹ m = 4.97×10⁻¹⁹ J

J·s × m/s leaves J·m; dividing by m leaves J.

Dr. Karmach

Worked example 2 — solution

E = h · c / λ
given: λ = 400 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E
Step 1 · Identify the given Step 2 · Choose the formula Step 3 · Substitute and cancel units
E = 6.626×10⁻³⁴ J·s × 3.00×10⁸ m/s400×10⁻⁹ m = 4.97×10⁻¹⁹ J
Step 4 · Check the size
Violet light (400 nm) lands near 5×10⁻¹⁹ J per photon. A shorter wavelength carries more energy, and 400 nm is near the short end of visible light. ✓
Dr. Karmach

Your turn — energy of a green photon

E = h · c / λ
given: λ = 500 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E

A photon of green light has a wavelength of 500 nm. (1 m = 10⁹ nm)

E = 6.626×10⁻³⁴ J·s × 3.00×10⁸ m/s m = J

Convert 500 nm to meters, fill the denominator, then compute.

Dr. Karmach

Your turn — energy of a green photon

E = h · c / λ
given: λ = 500 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E

A photon of green light has a wavelength of 500 nm. (1 m = 10⁹ nm)

E = 6.626×10⁻³⁴ J·s × 3.00×10⁸ m/s m = J

Convert 500 nm to meters, fill the denominator, then compute.

E = 6.626×10⁻³⁴ J·s × 3.00×10⁸ m/s500×10⁻⁹ m = 3.98×10⁻¹⁹ J
Green light (500 nm) sits mid-spectrum, and its photon energy lands mid-range too, near 4×10⁻¹⁹ J. ✓
Dr. Karmach

Where this goes wrong

E = h · c / λ
λ = 400 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · correct E = 4.97×10⁻¹⁹ J
Stopping at the frequency. ν = c/λ = 7.50×10¹⁴ s⁻¹ is only the frequency, one step short. Finish with E = hν: multiply by 6.626×10⁻³⁴ J·s so s⁻¹ and s cancel into joules.
Leaving the wavelength in nanometers. Dividing by 400 instead of 400×10⁻⁹ m gives 4.97×10⁻²⁸ J — smaller by a factor of 10⁹. Convert first: 400 nm × (1 m / 10⁹ nm).
Pairing energy with wavelength. E = hλ = 2.65×10⁻⁴⁰ has units of J·s·m, not joules. Energy pairs with frequency: E = hν, or E = hc/λ.
Dr. Karmach

Practice 1

E = h · c / λ
given: λ = 450 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s · wanted: E

A photon of blue light has a wavelength of 450 nm. What is its energy? (1 m = 10⁹ nm)

  1. 6.67 × 10¹⁴ s⁻¹
  2. 4.42 × 10⁻²⁸ J
  3. 4.42 × 10⁻¹⁹ J
  4. 2.98 × 10⁻⁴⁰ J·s·m
Dr. Karmach

Practice 1 — answer: C

E = h · c / λ
given: λ = 450 nm · λ = 450×10⁻⁹ m · wanted: E
E = 6.626×10⁻³⁴ J·s × 3.00×10⁸ m/s450×10⁻⁹ m = 4.42×10⁻¹⁹ J — answer C

A stopped at the frequency: ν = c/λ = 6.67×10¹⁴ s⁻¹, one step short of energy. B left the wavelength in nanometers: dividing by 450 instead of 450×10⁻⁹ m gives 4.42×10⁻²⁸ J, too small by 10⁹. D paired energy with wavelength: E = hλ = 2.98×10⁻⁴⁰ J·s·m, not joules.

Blue light (450 nm) carries about 4×10⁻¹⁹ J per photon. A shorter wavelength carries more energy, and blue sits toward the short end of visible light. ✓
Dr. Karmach

Worked example 3 — comparing two photons

E = h · c / λ
red λ = 650 nm · ultraviolet λ = 325 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s

A red photon has a wavelength of 650 nm; an ultraviolet photon has a wavelength of 325 nm. Which carries more energy, and by how much?

A common first attempt: the 650 nm photon has the larger number, so call it the more energetic one. Test it.

Dr. Karmach

Worked example 3 — solution

E = h · c / λ
red λ = 650 nm · ultraviolet λ = 325 nm · wanted: which E is larger

A common first attempt

650 is a bigger number than 325, so the red photon looks more energetic. But λ sits in the denominator of E = hc/λ, so a bigger λ makes a smaller E.

Dr. Karmach

Worked example 3 — solution

E = h · c / λ
red λ = 650 nm · ultraviolet λ = 325 nm · wanted: which E is larger
A common first attempt Step 1 · Identify the given

Convert each wavelength to meters: 650 nm → 650×10⁻⁹ m, and 325 nm → 325×10⁻⁹ m. The unknown is which energy is larger.

Dr. Karmach

Worked example 3 — solution

E = h · c / λ
red λ = 650 nm · ultraviolet λ = 325 nm · wanted: which E is larger
A common first attempt Step 1 · Identify the given Step 2 · Choose the formula

Both photons use E = hc/λ, with the same h and c. Only λ differs, and 325 nm is exactly half of 650 nm.

λ in the denominator means the shorter 325 nm wavelength gives the larger energy, not the longer 650 nm one. ✓
Dr. Karmach

Worked example 3 — which carries more

E = h · c / λ
red λ = 650×10⁻⁹ m · ultraviolet λ = 325×10⁻⁹ m

Step 3 · Substitute and cancel units

Ered = 6.626×10⁻³⁴ × 3.00×10⁸650×10⁻⁹ = 3.06×10⁻¹⁹ J
EUV = 6.626×10⁻³⁴ × 3.00×10⁸325×10⁻⁹ = 6.12×10⁻¹⁹ J
Dr. Karmach

Worked example 3 — which carries more

E = h · c / λ
red λ = 650×10⁻⁹ m · ultraviolet λ = 325×10⁻⁹ m

Step 3 · Substitute and cancel units

Ered = 6.626×10⁻³⁴ × 3.00×10⁸650×10⁻⁹ = 3.06×10⁻¹⁹ J
EUV = 6.626×10⁻³⁴ × 3.00×10⁸325×10⁻⁹ = 6.12×10⁻¹⁹ J
Same numerator, smaller wavelength — the larger energy goes to the ultraviolet photon. ✓
Dr. Karmach

Worked example 3 — which carries more

E = h · c / λ
red λ = 650×10⁻⁹ m · ultraviolet λ = 325×10⁻⁹ m

Step 4 · Check the size

Half the wavelength, double the energy: 650 / 325 = 2, and 6.12×10⁻¹⁹ J is twice 3.06×10⁻¹⁹ J. The ultraviolet photon carries the larger energy, and that is why ultraviolet burns skin and the red light beside it does not. ✓
Dr. Karmach

Take-home: shorter wavelength, more energy

E = h · c / λ
λ sits in the denominator: as λ falls, E rises
650 nm → 3.06×10⁻¹⁹ J · 325 nm → 6.12×10⁻¹⁹ J
halve the wavelength, double the energy per photon

Wavelength sits in the denominator, so a shorter wavelength means a larger energy. This is why ultraviolet damages skin while the visible light beside it does not.

Dr. Karmach

Practice 2

E = h · c / λ
photon A: λ = 600 nm · photon B: λ = 200 nm · h = 6.626×10⁻³⁴ J·s · c = 3.00×10⁸ m/s

Photon A has a wavelength of 600 nm; photon B has a wavelength of 200 nm. Which carries more energy, and how much more?

  1. Photon A, because its wavelength is larger.
  2. Photon B, and it carries three times the energy.
  3. They carry equal energy; the beams differ only in brightness.
  4. Photon B, and it carries nine times the energy.
Dr. Karmach

Practice 2 — answer: B

E = h · c / λ
photon A: λ = 600×10⁻⁹ m · photon B: λ = 200×10⁻⁹ m
EB = 6.626×10⁻³⁴ × 3.00×10⁸200×10⁻⁹ = 9.94×10⁻¹⁹ J — answer B

A reads λ backwards: the larger 600 nm sits in the denominator, so it gives the smaller energy, 3.31×10⁻¹⁹ J. C counts brightness as energy; brightness is the number of photons, not the energy of each. D squares the ratio: energy scales as 1/λ, so 600 / 200 = 3 times, not nine.

Photon B's 200 nm is one-third of A's 600 nm, so its energy is three times as large: 3 × 3.31×10⁻¹⁹ J = 9.94×10⁻¹⁹ J. ✓
Dr. Karmach

Check yourself

  1. A photon's frequency doubles. What happens to its energy, and which formula tells you in one line?
  2. Two photons: one at 350 nm, one at 700 nm. Without a calculator, which carries more energy, and roughly how many times more?

When an electron drops from a higher energy level to a lower one inside an atom, it emits a photon whose energy is exactly the gap between the levels. E = hc/λ then turns that gap into the color of light you see.

Dr. Karmach

3 · The Bohr Model & Line Spectra

Explain why an excited hydrogen atom emits a line spectrum rather than a continuous one, and calculate the energy of the photon released when an electron falls between principal energy levels.

Dr. Karmach

Two kinds of glow

A lightbulb pours out every color — a smooth rainbow. A tube of hydrogen gas glows too, but a prism splits it into just a few lines. Why skip the rest?

Dr. Karmach

Line vs. continuous spectra

A continuous spectrum holds every wavelength, no gaps — light from a hot solid.
A line spectrum holds only a few wavelengths, bright lines in the dark — light from excited, low-pressure gas atoms.

continuous → every wavelength  ·  line → only a few
the gaps are the clue: an atom can release only certain photon energies
Dr. Karmach

Bohr's idea

Bohr pictured the electron on a ladder of fixed energy levels, never between rungs. Falling to a lower level emits the gap as one photon; only certain gaps exist, so only certain lines appear.

Dr. Karmach

The energy of a level — and of a jump

Each hydrogen level has a fixed energy:

Eₙ = −2.18×10⁻¹⁸ J × (1/n²)
n = 1 is deepest (−2.18×10⁻¹⁸ J); higher levels crowd toward 0

A jump changes the energy by the difference between the levels:

ΔE = −2.18×10⁻¹⁸ J × (1/n_f² − 1/nᵢ²)
emission: n_f < nᵢ → ΔE negative; the photon carries |ΔE|

Bigger drops release more energy and shorter wavelengths.

Dr. Karmach

Which series lands where

The final level fixes the region of the spectrum.

to n = 1 → ultraviolet (Lyman)
to n = 2 → visible (Balmer) · to n = 3 → infrared (Paschen)

Jumps ending on n = 2 give the visible lines your eye can see; those ending on n = 1 are higher-energy ultraviolet.

Dr. Karmach

The method

  1. Identify nᵢ and n_f. Emission means n_f is the lower level.
  2. Compute 1/n_f² and 1/nᵢ². Square, then invert.
  3. Subtract: (1/n_f² − 1/nᵢ²).
  4. Multiply by −2.18×10⁻¹⁸ J. ΔE is negative; the photon carries its magnitude.
Dr. Karmach

Worked example 1 — n = 3 → n = 2

hydrogen: nᵢ = 3 → n_f = 2
given: the two levels · wanted: ΔE and the emitted photon's energy

This is the first line of the Balmer series. Find the energy released, then place it in the spectrum.

Dr. Karmach

Worked example 1 — solution

nᵢ = 3,   n_f = 2
emission — the electron drops to the lower level

Step 1 · Identify nᵢ and n_f

Start at nᵢ = 3, end at n_f = 2. The final level is lower, so a photon leaves.

Dr. Karmach

Worked example 1 — solution

nᵢ = 3,   n_f = 2
emission — the electron drops to the lower level
Step 1 · Identify nᵢ and n_f Step 2 · Compute 1/n_f² and 1/nᵢ²

1/n_f² = 1/2² = 0.2500 and 1/nᵢ² = 1/3² = 0.1111.

Dr. Karmach

Worked example 1 — solution

nᵢ = 3,   n_f = 2
emission — the electron drops to the lower level
Step 1 · Identify nᵢ and n_f Step 2 · Compute 1/n_f² and 1/nᵢ² Step 3 · Subtract
1/2² − 1/3² = 0.2500 − 0.1111 = 0.1389
Dr. Karmach

Worked example 1 — solution

nᵢ = 3,   n_f = 2
emission — the electron drops to the lower level
Step 1 · Identify nᵢ and n_f Step 2 · Compute 1/n_f² and 1/nᵢ² Step 3 · Subtract
1/2² − 1/3² = 0.2500 − 0.1111 = 0.1389
Step 4 · Multiply by −2.18×10⁻¹⁸ J
ΔE = −2.18×10⁻¹⁸ J × 0.1389 = −3.03×10⁻¹⁹ J
negative → the atom loses energy · the photon carries |ΔE| = 3.03×10⁻¹⁹ J
3.03×10⁻¹⁹ J is a visible photon (λ ≈ 656 nm, red) — hydrogen's red Balmer line. A small gap gives low energy and a long wavelength.
Dr. Karmach

Worked example 2 — n = 4 → n = 1

hydrogen: nᵢ = 4 → n_f = 1
given: the two levels · wanted: ΔE and the photon's region

Same equation, a much bigger drop — all the way down to the ground level. Predict where this photon lands.

Dr. Karmach

Worked example 2 — solution

nᵢ = 4,   n_f = 1
a Lyman jump — down to the ground level n = 1

Step 1 · Identify nᵢ and n_f

Start at nᵢ = 4, end at n_f = 1.

Dr. Karmach

Worked example 2 — solution

nᵢ = 4,   n_f = 1
a Lyman jump — down to the ground level n = 1
Step 1 · Identify nᵢ and n_f Step 2 · Compute 1/n_f² and 1/nᵢ²

1/n_f² = 1/1² = 1.0000 and 1/nᵢ² = 1/4² = 0.0625.

Dr. Karmach

Worked example 2 — solution

nᵢ = 4,   n_f = 1
a Lyman jump — down to the ground level n = 1
Step 1 · Identify nᵢ and n_f Step 2 · Compute 1/n_f² and 1/nᵢ² Step 3 · Subtract
1/1² − 1/4² = 1.0000 − 0.0625 = 0.9375
Dr. Karmach

Worked example 2 — solution

nᵢ = 4,   n_f = 1
a Lyman jump — down to the ground level n = 1
Step 1 · Identify nᵢ and n_f Step 2 · Compute 1/n_f² and 1/nᵢ² Step 3 · Subtract
1/1² − 1/4² = 1.0000 − 0.0625 = 0.9375
Step 4 · Multiply by −2.18×10⁻¹⁸ J
ΔE = −2.18×10⁻¹⁸ J × 0.9375 = −2.04×10⁻¹⁸ J
photon = 2.04×10⁻¹⁸ J — far more than any Balmer jump
2.04×10⁻¹⁸ J lands in the ultraviolet (λ ≈ 97 nm), the Lyman series. The bigger the drop, the more energy and the shorter the wavelength.
Dr. Karmach

Your turn — n = 4 → n = 2

Fill each blank, then confirm the photon lands in the visible range.

1/2² − 1/4² = 0.2500 − =
quantity value
1/n_f² = 1/2² 0.2500
1/nᵢ² = 1/4²
difference
ΔE
Dr. Karmach

Your turn — n = 4 → n = 2

Fill each blank, then confirm the photon lands in the visible range.

1/2² − 1/4² = 0.2500 − =
quantity value
1/n_f² = 1/2² 0.2500
1/nᵢ² = 1/4²
difference
ΔE
ΔE = −2.18×10⁻¹⁸ J × (0.2500 − 0.0625) = −2.18×10⁻¹⁸ × 0.1875 = −4.09×10⁻¹⁹ J
photon = 4.09×10⁻¹⁹ J ≈ 486 nm, blue-green — the second Balmer line
Dr. Karmach

Where this goes wrong

Forgetting to square n. Using (1/n_f − 1/nᵢ) instead of (1/n_f² − 1/nᵢ²) changes the answer. For 3 → 2 that gives 0.1667, not 0.1389 — a different, wrong energy. Square each n first.
Subtracting in the wrong order. Writing (1/nᵢ² − 1/n_f²) flips the sign of ΔE. Keep final minus initial: (1/n_f² − 1/nᵢ²).
Reporting ΔE as the photon's energy. ΔE for emission is negative because the atom loses energy. The photon it emits carries the positive magnitude, |ΔE|. A photon never has negative energy.
Expecting a continuous rainbow. A lone excited atom can release only fixed gaps, so it emits lines, not a smear. The rainbow comes from hot solids, not from single atoms.
Dr. Karmach

Practice 1 — shortest wavelength

Each transition emits a photon. Which emitted photon has the shortest wavelength?

  1. n = 2 → n = 1
  2. n = 3 → n = 2
  3. n = 4 → n = 2
  4. n = 5 → n = 2
Dr. Karmach

Practice 1 — answer: A

Shortest wavelength means highest energy, which means the biggest (1/n_f² − 1/nᵢ²).

A: 1/1² − 1/2² = 0.7500 → ΔE = −1.64×10⁻¹⁸ J
a UV photon — larger than every Balmer jump below it

B, C, and D all land on n = 2 (visible): 3→2 = 3.03×10⁻¹⁹ J, 4→2 = 4.09×10⁻¹⁹ J, 5→2 = 4.58×10⁻¹⁹ J — each smaller than A, so each a longer wavelength.

A drops all the way to n = 1, the largest gap in the set, so it carries the most energy and the shortest wavelength.
Dr. Karmach

Practice 2 — which is visible?

Which transition emits a photon of visible light?

  1. n = 2 → n = 1
  2. n = 3 → n = 2
  3. n = 4 → n = 3
  4. n = 5 → n = 4
Dr. Karmach

Practice 2 — answer: B

Only jumps that land on n = 2 (the Balmer series) fall in the visible range.

n = 3 → n = 2 ⇒ visible (656 nm, red)
to n = 2 → visible · to n = 1 → UV · to n = 3 → infrared

A (2 → 1) is a Lyman jump — ultraviolet. C (4 → 3) and D (5 → 4) land on n = 3 or higher — infrared. Only B lands on n = 2.

Where a jump ends sets its region: n = 2 is visible, n = 1 is ultraviolet, n = 3 and up are infrared.
Dr. Karmach

Check yourself

  1. An electron in hydrogen falls from n = 5 to n = 2. Compute ΔE, and state whether the photon is visible or ultraviolet.
  2. In one sentence, explain why hydrogen produces a line spectrum instead of a continuous one.

Every element has its own set of energy-level gaps, so every element has its own line-spectrum fingerprint. Those fixed levels are the seed of the quantum-number rules and orbital shapes that come next.

Dr. Karmach

4 · Quantum Numbers

Assign a valid set of quantum numbers (n, ℓ, mℓ, mₛ) to any electron, and explain what those numbers and the Heisenberg uncertainty principle say about where an electron is.

Dr. Karmach

Every electron has an address

A mailing address narrows a location step by step — state, city, street, house. Four quantum numbers place an electron the same way: shell, subshell, orbital, spin.

Dr. Karmach

Four numbers, four questions

Each quantum number answers one question, and each one narrows the electron's location further than the last.

n · ℓ · mℓ · mₛ
shell → subshell → orbital → spin — the complete address of one electron
  • n — which shell (its size and energy): 1, 2, 3, …
  • — which subshell (its shape): 0 up to n−1, written s, p, d, f
  • mℓ — which orbital (its orientation): −ℓ up to +ℓ
  • mₛ — which spin: +½ or −½
Dr. Karmach

The rules chain together

Each number's allowed range depends on the one before it. ℓ can never reach n, and mℓ can never exceed ℓ. Read the tree left to right: the shell sets what subshells exist, and each subshell sets how many orbitals it has.

Dr. Karmach

Why an address, not a path

Δx · Δp ≥ ħ/2
Heisenberg's uncertainty principle — an electron's position and momentum cannot both be pinned down at once

The more precisely we fix where an electron is (Δx small), the less we can know about where it is going (Δp large). So we never draw an electron on a fixed orbit. Instead we give its orbital — a region where it is found about 90% of the time. The quantum numbers name that region; they are the electron's neighborhood, not its moment-by-moment position.

Dr. Karmach

What each number tells you

  • n sets the shell's size and energy — larger n means larger and higher in energy.
  • sets the orbital's shape — s is spherical, p is a dumbbell, d is a cloverleaf.
  • mℓ sets its orientation in space — the three p orbitals point along x, y, z.
  • mₛ sets the electron's spin direction, drawn ↑ or ↓.

Two electrons sharing one orbital match on n, ℓ, and mℓ, so they must differ in mₛ. No two electrons in an atom carry the same four numbers — the Pauli exclusion principle.

Dr. Karmach

The method — assign a valid set

  1. n = the shell number — the digit written in the sublevel (the 3 in 3d).
  2. = the subshell letter as a number: s = 0, p = 1, d = 2, f = 3. Check that ℓ ≤ n−1.
  3. mℓ = any whole number from −ℓ to +ℓ (including 0). Check that |mℓ| ≤ ℓ.
  4. mₛ = +½ or −½.
Dr. Karmach

Worked example 1 — a 3d electron

an electron in a 3d orbital
wanted: one valid set of quantum numbers (n, ℓ, mℓ, mₛ)

Give a complete set of four quantum numbers that could describe this electron. Read the label 3d, then apply each rule in turn.

Dr. Karmach

Worked example 1 — solution

Step 1 · n from the shell number

The digit in 3d is the shell: n = 3.

Dr. Karmach

Worked example 1 — solution

Step 1 · n from the shell number
Step 2 · ℓ from the letter

d is the third subshell type, so ℓ = 2. Check the rule: ℓ ≤ n−1 = 2 ✓.

Dr. Karmach

Worked example 1 — solution

Step 1 · n from the shell number
Step 2 · ℓ from the letter
Step 3 · mℓ from −ℓ to +ℓ Step 4 · mₛ = +½ or −½

mℓ may be any of −2, −1, 0, +1, +2. Choose one — say mℓ = +1 — and a spin, mₛ = +½.

(n, ℓ, mℓ, mₛ) = (3, 2, +1, +½)
a valid set · n and ℓ are fixed by "3d"; mℓ and mₛ pick the seat
Dr. Karmach

Worked example 1 — solution

Step 1 · n from the shell number
Step 2 · ℓ from the letter
Step 3 · mℓ from −ℓ to +ℓ Step 4 · mₛ = +½ or −½

(n, ℓ, mℓ, mₛ) = (3, 2, +1, +½)
a valid set · n and ℓ are fixed by "3d"; mℓ and mₛ pick the seat
The 3d subshell holds (2×2+1) × 2 = 10 electrons — 5 orbitals, 2 spins each — so ten different valid sets share n = 3, ℓ = 2. The label fixes n and ℓ; mℓ and mₛ choose among the openings.
Dr. Karmach

Worked example 2 — is this set allowed?

n = 2, ℓ = 2, mℓ = 0, mₛ = +½
decide: valid or forbidden — and name the rule

A student writes this set for an electron. Check each number against its rule before accepting it.

Dr. Karmach

Worked example 2 — solution

Check ℓ against n

The rule is ℓ ≤ n−1. Here n = 2, so ℓ can only be 0 or 1 — the 2s and 2p subshells. There is no 2d.

ℓ = 2 with n = 2 → n−1 = 1, but 2 > 1 ✗
forbidden — ℓ has reached n, which the rule never allows
Dr. Karmach

Worked example 2 — solution

Check ℓ against n

ℓ = 2 with n = 2 → n−1 = 1, but 2 > 1 ✗
forbidden — ℓ has reached n, which the rule never allows
The fix

To carry ℓ = 2 (a d subshell), an electron needs a shell that actually contains d — the first is n = 3. Change n to 3, or change ℓ to 0 or 1.

mℓ = 0 and mₛ = +½ are both fine on their own. One broken rule — ℓ too large for its shell — is enough to forbid the whole set.
Dr. Karmach

Your turn — a 4p electron

An electron sits in a 4p orbital. Fill each quantum number, checking it against its rule.

quantum number value
n
mℓ (choose one)
mₛ
Dr. Karmach

Your turn — a 4p electron

An electron sits in a 4p orbital. Fill each quantum number, checking it against its rule.

quantum number value
n
mℓ (choose one)
mₛ
n = 4, ℓ = 1, mℓ = −1 (or 0 or +1), mₛ = +½ (or −½)
4 → n = 4 · p → ℓ = 1 (≤ 3 ✓) · mℓ from −1 to +1 · spin ±½
Dr. Karmach

Where this goes wrong

Letting ℓ equal n. For n = 3, writing ℓ = 3 is forbidden — ℓ stops at n−1 = 2. The subshells in n = 3 are only s, p, d (ℓ = 0, 1, 2).
Pushing mℓ past ℓ. A p subshell has ℓ = 1, so mℓ is −1, 0, or +1. Writing mℓ = +2 for a p electron breaks |mℓ| ≤ ℓ; +2 first appears in a d subshell.
Giving mₛ any value but ±½. Spin is only +½ or −½. A "0" or "+1" for mₛ is never allowed — an electron has exactly two spin states.
Reading mℓ's range from n. mℓ runs from −ℓ to +ℓ, not −n to +n. It is ℓ, the shape number, that sets how many orbitals a subshell has (2ℓ+1).
Dr. Karmach

Practice 1

Which set of quantum numbers is not allowed for an electron in an atom?

  1. n = 3, ℓ = 2, mℓ = −2, mₛ = +½
  2. n = 2, ℓ = 1, mℓ = 0, mₛ = −½
  3. n = 1, ℓ = 1, mℓ = 0, mₛ = +½
  4. n = 4, ℓ = 0, mℓ = 0, mₛ = −½
Dr. Karmach

Practice 1 — answer: C

n = 1, ℓ = 1 → n−1 = 0, but ℓ = 1 ✗
answer C — the n = 1 shell holds only ℓ = 0 (the 1s subshell)

C fails ℓ ≤ n−1: with n = 1 the only allowed ℓ is 0, so there is no "1p." A is a legal 3d electron (ℓ = 2 needs n ≥ 3 ✓, mℓ = −2 is within −2…+2). B is a legal 2p electron. D is a legal 4s electron. Each of those obeys every rule.

Scan the set in order: ℓ against n first, then mℓ against ℓ, then mₛ. C breaks at the very first check.
Dr. Karmach

Practice 2

An electron occupies a 4f orbital. Which set of quantum numbers could describe it?

  1. n = 4, ℓ = 3, mℓ = −3, mₛ = +½
  2. n = 4, ℓ = 4, mℓ = 0, mₛ = +½
  3. n = 3, ℓ = 3, mℓ = +1, mₛ = −½
  4. n = 4, ℓ = 3, mℓ = +4, mₛ = +½
Dr. Karmach

Practice 2 — answer: A

4f → n = 4, ℓ = 3, mℓ from −3 to +3, mₛ = ±½
answer A — n = 4, ℓ = 3, mℓ = −3 obeys every rule

An f subshell is ℓ = 3, which first appears at n = 4. A fits: ℓ = 3 ≤ n−1 = 3, and mℓ = −3 lies within −3…+3. B sets ℓ = 4, but ℓ can only reach n−1 = 3. C puts ℓ = 3 in n = 3, where ℓ stops at 2 — there is no 3f. D pushes mℓ = +4 past ℓ = 3.

The 4f subshell holds 2×3+1 = 7 orbitals and 14 electrons, so mℓ ranges across seven values, −3 through +3 — never ±4.
Dr. Karmach

Check yourself

  1. Give one valid set of quantum numbers for an electron in a 2p orbital, and state how many valid sets a full 2p subshell allows.
  2. Why is the set n = 3, ℓ = 0, mℓ = +1, mₛ = +½ forbidden? Name the rule it breaks.

The four quantum numbers label every electron uniquely, and no two in an atom share all four. Filling those addresses from the lowest energy upward — 1s, then 2s, then 2p — builds the atom's electron configuration.

Dr. Karmach

5 · Orbital Shapes & Nodes

Describe the shapes of s, p, and d orbitals and count their nodes, using nodal planes = ℓ and total nodes = n − 1.

Dr. Karmach

The shape of an electron cloud

An electron is not a dot on a fixed path. The best we can do is map the region where it is likely to be. That region has a definite shape, set by the sublevel.

Dr. Karmach

An orbital is a region of probability

An orbital is the region around the nucleus where an electron most likely is — drawn to enclose about 90% of its probability. The sublevel sets the shape: s a sphere, p a dumbbell on an axis, d a cloverleaf.

The p sublevel holds three of these dumbbells, one aimed along each axis.

Dr. Karmach

Nodes: where the probability is zero

A node is a surface where the electron's probability drops to zero. The number of nodal planes through the nucleus equals ℓ. The total number of nodes in an orbital equals n − 1.

nodal planes = ℓ
s → 0 · p → 1 · d → 2 · a flat surface cutting through the nucleus
total nodes = n − 1
= (nodal planes = ℓ) + (radial nodes = n − ℓ − 1) · a 1s orbital has 1 − 1 = 0 nodes
Dr. Karmach

The method

  1. Read n and ℓ. The sublevel gives ℓ: s = 0, p = 1, d = 2.
  2. Nodal planes = ℓ. These flat surfaces pass through the nucleus.
  3. Total nodes = n − 1.
  4. Radial nodes = total − nodal planes = n − ℓ − 1. These are spherical shells.
Dr. Karmach

Worked example 1 — the 3p orbital

Step 1 · Read n and ℓ

3p orbital
n = 3 · p → ℓ = 1 · wanted: nodal planes and total nodes

Find how many nodal planes the 3p orbital has, then how many nodes it has in all.

Dr. Karmach

Worked example 1 — solution

3p orbital
n = 3 · ℓ = 1

Step 2 · Nodal planes = ℓ

ℓ = 1, so the 3p orbital has one nodal plane — the flat surface through the nucleus that splits its two lobes.

nodal planes = ℓ = 1
every p orbital has exactly 1 nodal plane, the same as 2p
Dr. Karmach

Worked example 1 — solution

3p orbital
n = 3 · ℓ = 1

Step 2 · Nodal planes = ℓ

ℓ = 1, so the 3p orbital has one nodal plane — the flat surface through the nucleus that splits its two lobes.

nodal planes = ℓ = 1
every p orbital has exactly 1 nodal plane, the same as 2p
Step 3 · Total nodes = n − 1
total nodes = n − 1 = 3 − 1 = 2
1 nodal plane (ℓ = 1) + 1 radial node (n − ℓ − 1 = 1) = 2 ✓
Dr. Karmach

Where this goes wrong

Confusing nodal planes with total nodes. A 3p orbital has ℓ = 1, so 1 nodal plane — but its total is n − 1 = 2. The extra node is a radial (spherical) node.
Giving a d orbital 0 nodal planes. A cloverleaf needs 2 planes to separate its four lobes: nodal planes = ℓ = 2. For 3d, radial nodes = 3 − 2 − 1 = 0, so both of its nodes are planes.
Reading the 2p total as 2. A 2p orbital has n = 2, so n − 1 = 1 node — its single nodal plane. Radial nodes = 2 − 1 − 1 = 0; there are none.
Thinking px, py, and pz have different shapes. They are one identical dumbbell, differing only in the axis they point along.
Dr. Karmach

6 · Sublevels & Orbitals

Count the orbitals and the maximum electrons in any sublevel or shell, using that every orbital holds two electrons.

Dr. Karmach

Filling a concert hall

A concert hall fills one section at a time. Each section holds a fixed number of seats. Add the seats section by section, and the hall's capacity is known exactly.

Dr. Karmach

One orbital, at most two electrons

An electron shell is divided into sublevels. Each sublevel is built from orbitals, and every orbital holds at most two electrons. That single limit fixes every capacity that follows.

1 orbital → 2 electrons maximum
the two electrons pair with opposite spins — no orbital holds a third
Dr. Karmach

Four sublevels, four orbital counts

The sublevels are named s, p, d, and f. Each is built from a fixed number of orbitals: 1, 3, 5, or 7. Double the count for its electron capacity.

Dr. Karmach

A shell holds 2n² electrons

Shell number n contains exactly n sublevels. Their orbitals total n², and since each orbital holds two electrons, the shell's capacity is 2n². Add the sublevels or use the formula — the count matches.

Dr. Karmach

The method

  1. Name the sublevel. The type sets its orbitals: s = 1, p = 3, d = 5, f = 7.
  2. Double the orbitals. Each orbital holds 2 electrons.
  3. For a whole shell, add its sublevels, or use 2n².
Dr. Karmach

Worked example 1 — the 3p sublevel

3p sublevel
given: a p-type sublevel · wanted: its maximum electrons

Filled completely, how many electrons does the 3p sublevel hold? Name the type, then count.

Dr. Karmach

Worked example 1 — solution

3p sublevel
given: a p-type sublevel · wanted: its maximum electrons

Step 1 · Name the sublevel

A p sublevel always has 3 orbitals. The 3 in front is the shell number and does not change that count.

Dr. Karmach

Worked example 1 — solution

3p sublevel
given: a p-type sublevel · wanted: its maximum electrons
Step 1 · Name the sublevel Step 2 · Double the orbitals
3 orbitals × 2 = 6 electrons
each orbital holds 2 · a full 3p sublevel holds 6
Dr. Karmach

Worked example 1 — solution

3p sublevel
given: a p-type sublevel · wanted: its maximum electrons
Step 1 · Name the sublevel Step 2 · Double the orbitals
3 orbitals × 2 = 6 electrons
each orbital holds 2 · a full 3p sublevel holds 6
Three orbitals, two electrons apiece. Six is the most the 3p sublevel can hold, the same as any p sublevel.
Dr. Karmach

Worked example 2 — the 3d sublevel

3d sublevel
given: a d-type sublevel · wanted: its maximum electrons

A d sublevel has 5 orbitals. A common first attempt: 5 orbitals, so 5 electrons. Name the type, then count carefully.

Dr. Karmach

Worked example 2 — solution

3d sublevel
given: a d-type sublevel · wanted: its maximum electrons

A common first attempt

5 orbitals → 5 electrons?
that counts orbitals, not electrons — each orbital still holds 2 ✗

Five is the orbital count, not the electron count. Every orbital holds two electrons, so the two numbers cannot be equal.

Dr. Karmach

Worked example 2 — solution

3d sublevel
given: a d-type sublevel · wanted: its maximum electrons
A common first attempt
5 orbitals → 5 electrons?
that counts orbitals, not electrons — each orbital still holds 2 ✗
Step 1 · Name the sublevel

A d sublevel has 5 orbitals, two more than a p sublevel.

Dr. Karmach

Worked example 2 — solution

3d sublevel
given: a d-type sublevel · wanted: its maximum electrons
A common first attempt
5 orbitals → 5 electrons?
that counts orbitals, not electrons — each orbital still holds 2 ✗
Step 1 · Name the sublevel Step 2 · Double the orbitals
5 orbitals × 2 = 10 electrons
five orbitals, two electrons each · a full 3d sublevel holds 10
Dr. Karmach

Worked example 2 — solution

3d sublevel
given: a d-type sublevel · wanted: its maximum electrons
A common first attempt
5 orbitals → 5 electrons?
that counts orbitals, not electrons — each orbital still holds 2 ✗
Step 1 · Name the sublevel Step 2 · Double the orbitals
5 orbitals × 2 = 10 electrons
five orbitals, two electrons each · a full 3d sublevel holds 10
Ten, not five. The orbital count and the electron count differ by exactly the factor of two that every orbital carries.
Dr. Karmach

Take-home: orbitals are not electrons

5 orbitals ≠ 5 electrons
the d sublevel: 5 orbitals × 2 = 10 electrons

Orbitals and electrons are not the same count. A sublevel's orbital count answers "how many orbitals"; doubling it answers "how many electrons". Match the number to the question.

Dr. Karmach

Your turn — fill the n = 3 shell

the n = 3 shell: 3s, 3p, 3d
three sublevels — double each orbital count, then add
sublevel orbitals electrons
3s 1
3p 3
3d 5
whole shell 9

Double each orbital count, then total the shell.

Dr. Karmach

Your turn — fill the n = 3 shell

the n = 3 shell: 3s, 3p, 3d
three sublevels — double each orbital count, then add
sublevel orbitals electrons
3s 1
3p 3
3d 5
whole shell 9

Double each orbital count, then total the shell.

3s → 2 · 3p → 6 · 3d → 10 · shell → 2 + 6 + 10 = 18
18 = 2 × 3² — the sublevels add to the shell's 2n² capacity
Dr. Karmach

Where this goes wrong

Reporting orbitals as electrons. A d sublevel has 5 orbitals, so "5 electrons" looks right. Each orbital holds 2, so the count is 5 × 2 = 10 electrons.
Giving the whole shell's capacity for one sublevel. Asked for the 3d electrons, answering 18 reports the entire n = 3 shell. One sublevel is not the shell: 3d holds 10.
Using 2n for a shell instead of 2n². The n = 4 shell is not 2 × 4 = 8. Square n first: 2 × 4² = 32 electrons.
Miscounting d or f orbitals. A d sublevel has 5 orbitals, an f has 7, not the reverse. Calling d seven orbitals gives 7 × 2 = 14, too many.
Dr. Karmach

Practice 1

the 4p sublevel
a p-type sublevel in the n = 4 shell

Filled to capacity, how many electrons does the 4p sublevel hold?

  1. 3 electrons
  2. 6 electrons
  3. 16 electrons
  4. 32 electrons
Dr. Karmach

Practice 1 — answer: B

4p → 3 orbitals × 2 = 6 electrons — answer B
the 4 names the shell · a p sublevel always has 3 orbitals

A counted the 3 orbitals as electrons: a p sublevel has 3 orbitals, holding 3 × 2 = 6. C gave n² = 4² = 16, the orbitals in the whole n = 4 shell. D gave 2n² = 32, the electron capacity of the entire n = 4 shell, not one sublevel.

The 4p sublevel matches every p sublevel: 3 orbitals, 6 electrons. The shell number sets which shell, never the capacity of the sublevel.
Dr. Karmach

Worked example 3 — a full n = 4 shell

the n = 4 shell, completely filled
given: shell number n = 4 · wanted: total electrons

How many electrons fill the entire n = 4 shell? Find it two ways: add the sublevels, and apply the formula.

Dr. Karmach

Worked example 3 — solution

the n = 4 shell, completely filled
given: shell number n = 4 · wanted: total electrons

Step 1 · Name the sublevel

The n = 4 shell holds 4 sublevels: 4s, 4p, 4d, 4f — with 1, 3, 5, and 7 orbitals.

Dr. Karmach

Worked example 3 — solution

the n = 4 shell, completely filled
given: shell number n = 4 · wanted: total electrons
Step 1 · Name the sublevel Step 2 · Double the orbitals

Double each sublevel's orbitals: 4s gives 2, 4p gives 6, 4d gives 10, 4f gives 14.

Dr. Karmach

Worked example 3 — solution

the n = 4 shell, completely filled
given: shell number n = 4 · wanted: total electrons
Step 1 · Name the sublevel Step 2 · Double the orbitals Step 3 · For a whole shell, add its sublevels
2 + 6 + 10 + 14 = 32  ·  2 × 4² = 32
the sum and the formula 2n² agree — 32 electrons
Dr. Karmach

Worked example 3 — solution

the n = 4 shell, completely filled
given: shell number n = 4 · wanted: total electrons
Step 1 · Name the sublevel Step 2 · Double the orbitals Step 3 · For a whole shell, add its sublevels
2 + 6 + 10 + 14 = 32  ·  2 × 4² = 32
the sum and the formula 2n² agree — 32 electrons
Both routes reach 32. Adding the four sublevels and squaring the shell number are the same count, done two ways.
Dr. Karmach

Practice 2

the n = 3 shell, completely filled
given: shell number n = 3 · wanted: total electrons

How many electrons does a full n = 3 shell hold?

  1. 6 electrons
  2. 8 electrons
  3. 9 electrons
  4. 18 electrons
Dr. Karmach

Practice 2 — answer: D

n = 3: 2 + 6 + 10 = 18  ·  2 × 3² = 18 — answer D
3s, 3p, 3d hold 2, 6, 10 · the sum equals 2n²

A used 2n = 2 × 3 = 6, forgetting to square the shell number. B added only 3s and 3p, 2 + 6 = 8, dropping the 3d sublevel. C gave n² = 3² = 9, the orbital count for the shell, not its electrons.

The n = 3 shell adds a d sublevel that n = 2 lacks. Its 10 electrons carry the shell from 8 up to 18.
Dr. Karmach

Check yourself

  1. A full 4d sublevel: how many orbitals, and how many electrons? Name the type, then double.
  2. Which shell first includes an f sublevel, and what is that shell's total capacity, 2n²?

Every sublevel now has a known size. Filling them in order of increasing energy (1s, then 2s, then 2p) builds an atom's electron configuration, the ground-state arrangement of all its electrons.

Dr. Karmach

7 · Electron Configurations

Write the ground-state electron configuration of any atom through the d block, using the building-up order and noble-gas core notation.

Dr. Karmach

Filling from the ground up

A parking structure fills from the ground up. Every space on a lower level is taken before a single car parks on the level above.

Dr. Karmach

Lowest levels fill first

Electrons fill sublevels from the lowest energy up, each one completely before the next. Listing every sublevel with its electron count gives the electron configuration. The superscripts must add up to the atom's total.

neon: 1s²2s²2p⁶
2 + 2 + 6 = 10 electrons · neon's atomic number is 10 — the count matches ✓
Dr. Karmach

The building-up order

Sublevels do not fill in simple numerical order. They fill by increasing energy, which the diagonal arrows trace: 1s, 2s, 2p, 3s, 3p, then 4s before 3d. A few elements are exceptions to this order.

Dr. Karmach

Reading the order from the table

The periodic table follows this same order. Reading left to right across a period gives the sublevels in turn — s block, then d block, then p block.

Dr. Karmach

The method

  1. Count the electrons: a neutral atom's atomic number.
  2. Fill in the building-up order: 1s, 2s, 2p, 3s, 3p, 4s, 3d.
  3. Fill sublevels to capacity: s 2, p 6, d 10.
  4. Check the superscripts sum to the count.
Dr. Karmach

Worked example 1 — oxygen

Step 1 · Count the electrons

O — atomic number 8
a neutral atom has 8 electrons to place

Oxygen sits in the p block of period 2. Build its ground-state configuration from the lowest sublevel up.

Dr. Karmach

Worked example 1 — solution

O — atomic number 8
8 electrons to place

Step 2 · Fill in the building-up order

Start at the lowest sublevel and work up: 1s, then 2s, then 2p.

Dr. Karmach

Worked example 1 — solution

O — atomic number 8
8 electrons to place
Step 2 · Fill in the building-up order Step 3 · Fill sublevels to capacity

1s holds 2 and 2s holds 2. The remaining 4 electrons go into 2p, which holds up to 6.

1s²2s²2p⁴
2 + 2 + 4 = 8 electrons placed
Dr. Karmach

Worked example 1 — solution

O — atomic number 8
8 electrons to place
Step 2 · Fill in the building-up order Step 3 · Fill sublevels to capacity
1s²2s²2p⁴
2 + 2 + 4 = 8 electrons placed
Step 4 · Check the superscripts sum to the count

The superscripts total 8, matching oxygen's 8 electrons.

The final sublevel need not be full: 2p holds 6 but carries only 4 here. Configurations often end on a partly filled sublevel.
Dr. Karmach

Worked example 2 — iron

Step 1 · Count the electrons

Fe — atomic number 26
26 electrons to place

Iron is a d-block metal in period 4. After 3p⁶, 18 electrons are placed and 8 remain. A common first attempt sends all 8 straight into 3d. Build the full configuration.

Dr. Karmach

Worked example 2 — solution

Fe — atomic number 26
26 electrons to place

A common first attempt

Continuing straight from 3p into 3d:

1s²2s²2p⁶3s²3p⁶3d⁸
2 + 2 + 6 + 2 + 6 + 8 = 26 ✓ count · ✗ order — 4s is lower in energy than 3d
Dr. Karmach

Worked example 2 — solution

Fe — atomic number 26
26 electrons to place
A common first attempt
1s²2s²2p⁶3s²3p⁶3d⁸
2 + 2 + 6 + 2 + 6 + 8 = 26 ✓ count · ✗ order — 4s is lower in energy than 3d
Step 2 · Fill in the building-up order

The order places 4s before 3d. After 3p⁶, fill 4s, then 3d.

Dr. Karmach

Worked example 2 — solution

Fe — atomic number 26
26 electrons to place
A common first attempt
1s²2s²2p⁶3s²3p⁶3d⁸
2 + 2 + 6 + 2 + 6 + 8 = 26 ✓ count · ✗ order — 4s is lower in energy than 3d
Step 2 · Fill in the building-up order Step 3 · Fill sublevels to capacity Step 4 · Check the superscripts sum to the count

4s takes 2; the last 6 go into 3d, which holds up to 10. The superscripts total 26.

1s²2s²2p⁶3s²3p⁶4s²3d⁶
2 + 2 + 6 + 2 + 6 + 2 + 6 = 26 ✓ · matches iron's 26 electrons
Dr. Karmach

Worked example 2 — solution

Fe — atomic number 26
26 electrons to place
A common first attempt
1s²2s²2p⁶3s²3p⁶3d⁸
2 + 2 + 6 + 2 + 6 + 8 = 26 ✓ count · ✗ order — 4s is lower in energy than 3d
Step 2 · Fill in the building-up order Step 3 · Fill sublevels to capacity Step 4 · Check the superscripts sum to the count
1s²2s²2p⁶3s²3p⁶4s²3d⁶
2 + 2 + 6 + 2 + 6 + 2 + 6 = 26 ✓ · matches iron's 26 electrons
Both forms sum to 26, so the count alone cannot flag the error. The fixed order does: 4s fills before 3d.
Dr. Karmach

Take-home: 4s fills before 3d

Both forms here have the right electron count, yet only one follows the building-up order. Fill 4s before 3d.

✓ 1s²2s²2p⁶3s²3p⁶4s²3d⁶
2 + 2 + 6 + 2 + 6 + 2 + 6 = 26 · 4s before 3d — the building-up order
✗ 1s²2s²2p⁶3s²3p⁶3d⁸
2 + 2 + 6 + 2 + 6 + 8 = 26 · right count, wrong order
Dr. Karmach

Your turn — nickel

Nickel has atomic number 28. Fill the blanks, then confirm the superscripts sum to 28.

1s²2s²2p⁶3s²3p⁶4s3d
sublevel electrons
through 3p⁶ 18
4s
3d
Dr. Karmach

Your turn — nickel

Nickel has atomic number 28. Fill the blanks, then confirm the superscripts sum to 28.

1s²2s²2p⁶3s²3p⁶4s3d
sublevel electrons
through 3p⁶ 18
4s
3d
1s²2s²2p⁶3s²3p⁶4s²3d⁸
2 + 2 + 6 + 2 + 6 + 2 + 8 = 28 ✓ · 4s takes 2, then 3d takes 28 − 18 − 2 = 8
Dr. Karmach

Where this goes wrong

Filling 3d before 4s. For potassium, 19 electrons, writing 1s²2s²2p⁶3s²3p⁶3d¹ sums to 19, but 4s is lower in energy than 3d. The ground state is 1s²2s²2p⁶3s²3p⁶4s¹. The count passes; only the order catches this.
Superscripts that miss the count. Stopping calcium at 1s²2s²2p⁶3s²3p⁶ gives 2 + 2 + 6 + 2 + 6 = 18. That is argon, not calcium. Calcium, 20 electrons, needs 4s²: two more.
Overfilling a sublevel. Writing 2p⁸ to reach the count faster claims p holds 8. Each s holds 2, p holds 6, d holds 10. Move to the next sublevel when the current one is full.
Reading only the valence electrons. A configuration ending 3s²3p² has 4 valence electrons, but the atom is not element 4. Every superscript counts toward the atomic number, not just the last sublevel.
Dr. Karmach

Practice 1

1s²2s²2p⁶3s²3p²
a ground-state configuration

This configuration describes the ground state of which element?

  1. Silicon
  2. Aluminum
  3. Carbon
  4. Beryllium
Dr. Karmach

Practice 1 — answer: A

1s²2s²2p⁶3s²3p²
2 + 2 + 6 + 2 + 2 = 14 electrons — answer A, silicon (Z 14)

The superscripts add to 14, so the atomic number is 14: silicon. B, aluminum, has 13, one electron short: 2 + 2 + 6 + 2 + 1 = 13. C, carbon, shares the p² ending but sits a period higher, at 6: 2 + 2 + 2 = 6. D, beryllium, matches only the 4 valence electrons, not all 14.

The superscripts count every electron, not just the outer ones. Their sum, 14, is the atomic number.
Dr. Karmach

Noble-gas core notation

A configuration that begins with a noble gas can be abbreviated by that gas's symbol in brackets. [Ne] stands for 1s²2s²2p⁶; [Ar] for 1s²2s²2p⁶3s²3p⁶. Write the core, then the sublevels beyond it.

Na: 1s²2s²2p⁶3s¹ = [Ne]3s¹
[Ne] = 10 electrons · + 3s¹ = 11 total, sodium's count ✓
Dr. Karmach

Worked example 3 — titanium

Step 1 · Count the electrons

Ti — atomic number 22
22 electrons to place

Titanium is a d-block metal in period 4. Write its full ground-state configuration, then abbreviate it with a noble-gas core.

Dr. Karmach

Worked example 3 — solution

Ti — atomic number 22
22 electrons to place

Step 2 · Fill in the building-up order

Fill through 3p⁶, reaching 18 electrons, then 4s before 3d.

Dr. Karmach

Worked example 3 — solution

Ti — atomic number 22
22 electrons to place
Step 2 · Fill in the building-up order Step 3 · Fill sublevels to capacity

4s takes 2; the last 2 go into 3d.

1s²2s²2p⁶3s²3p⁶4s²3d²
2 + 2 + 6 + 2 + 6 + 2 + 2 = 22 electrons placed
Dr. Karmach

Worked example 3 — solution

Ti — atomic number 22
22 electrons to place
Step 2 · Fill in the building-up order Step 3 · Fill sublevels to capacity
1s²2s²2p⁶3s²3p⁶4s²3d²
2 + 2 + 6 + 2 + 6 + 2 + 2 = 22 electrons placed
Collapse to the noble-gas core Step 4 · Check the superscripts sum to the count

1s²2s²2p⁶3s²3p⁶ is argon, so it becomes [Ar]. The electrons still total 22.

[Ar]4s²3d²
[Ar] = 18 · 18 + 2 + 2 = 22 ✓ · titanium's 22 electrons
[Ar] hides 18 electrons but keeps them: 18 + 2 + 2 = 22, titanium's atomic number.
Dr. Karmach

Practice 2

V — atomic number 23
a d-block metal in period 4

Which is the correct ground-state configuration of vanadium?

  1. [Ar] 4s² 3d³
  2. [Ar] 3d⁵
  3. [Ar] 4s² 3d²
  4. [Ar] 4s² 4p³
Dr. Karmach

Practice 2 — answer: A

[Ar]4s²3d³
18 + 2 + 3 = 23 ✓ — answer A, vanadium's 23 electrons

After [Ar], 4s fills before 3d: 4s² then 3d³. B fills 3d before 4s; it sums to 23 (18 + 5) but breaks the order. C stops one electron short: 18 + 2 + 2 = 22, which is titanium. D skips 3d and fills 4p; it also sums to 23, but 3d is lower in energy than 4p.

The count alone passes B and D. The building-up order decides: 4s, then 3d, then 4p.
Dr. Karmach

Check yourself

  1. Write the ground-state configuration of sulfur (Z 16), and confirm the superscripts sum to 16.
  2. In period 4, which fills first, 4s or 3d? Give the noble-gas-core configuration of calcium (Z 20).

An element's configuration fixes its place in the periodic table. Its outermost electrons — the valence electrons — set atomic radius, ionization energy, and electronegativity, and these trend across periods and down groups.

Dr. Karmach

8 · Electron Configurations of Ions

Write the ground-state electron configuration of an ion — including transition-metal cations — by removing electrons from the highest principal level first, so that ns empties before (n−1)d.

Dr. Karmach

Emptying from the top

When cars leave a parking structure, the top floor empties first. Atoms lose electrons the same way — the highest-energy shell goes first, not the last one filled.

Dr. Karmach

A cation is a neutral atom, minus electrons

To write an ion's configuration, start from the neutral atom and remove one electron per unit of positive charge. Take them from the highest principal level n first — the outermost shell — then work inward.

Na: 1s²2s²2p⁶3s¹ → Na⁺: 1s²2s²2p⁶
remove the single n = 3 electron (the 3s) · 11 − 1 = 10 electrons, matching the 1+ charge

For main-group atoms the outermost electrons are also the last ones added, so nothing feels surprising — yet.

Dr. Karmach

The transition-metal twist: lose ns before (n−1)d

The building-up order fills 4s before 3d. Yet once 3d is occupied it sinks below 4s, leaving 4s as the outermost shell — the highest n, and so the first to leave.

remove the highest n first: n = 4 (the 4s) beats n = 3 (the 3d)
4s fills first, and 4s empties first — strip ns before touching (n−1)d

For any transition metal, take the ns electrons out before the (n−1)d.

Dr. Karmach

The method

  1. Write the neutral atom's configuration in noble-gas-core form.
  2. Count the charge: a 2+ ion has lost 2 electrons, a 3+ has lost 3.
  3. Remove from the highest n first — for a transition metal, empty ns before (n−1)d.
  4. Check: protons − electrons = the charge.
Dr. Karmach

Worked example — iron's cations

Fe — atomic number 26 → [Ar]4s²3d⁶
18 (argon core) + 2 + 6 = 26 electrons ✓

Iron gives up electrons to form Fe²⁺ and Fe³⁺. A common first attempt pulls them out of 3d, since 3d was filled last. Build both ions correctly.

Dr. Karmach

Worked example — solution

Fe²⁺ · remove 2 electrons, highest n first

The highest level is n = 4, holding 4s². Empty it — both electrons — before any 3d leaves.

Fe²⁺: [Ar]3d⁶
4s emptied, 3d untouched · 18 + 6 = 24 electrons · 26 − 24 = 2 → 2+ ✓
Dr. Karmach

Worked example — solution

Fe²⁺ · remove 2 electrons, highest n first

Fe²⁺: [Ar]3d⁶
4s emptied, 3d untouched · 18 + 6 = 24 electrons · 26 − 24 = 2 → 2+ ✓
Fe³⁺ · remove one more, now from 3d

With 4s already empty, the next-highest occupied level is 3d. Take one electron from it.

Fe³⁺: [Ar]3d⁵
18 + 5 = 23 electrons · 26 − 23 = 3 → 3+ ✓
Dr. Karmach

Worked example — solution

Fe²⁺ · remove 2 electrons, highest n first

Fe²⁺: [Ar]3d⁶
4s emptied, 3d untouched · 18 + 6 = 24 electrons · 26 − 24 = 2 → 2+ ✓
Fe³⁺ · remove one more, now from 3d
Fe³⁺: [Ar]3d⁵
18 + 5 = 23 electrons · 26 − 23 = 3 → 3+ ✓
Dr. Karmach

Where this goes wrong

Removing 3d before 4s. [Ar]4s²3d⁴ treats "last filled" as "first removed." Highest n leaves first: 4s before 3d. Fe²⁺ is [Ar]3d⁶.
Forgetting to start neutral. You can't remove from a shell never filled — write the full neutral configuration first, then subtract.
Miscounting the charge. A 3+ ion lost three electrons, not protons. Fe is always 26 p⁺; 26 − 23 e⁻ = 3+ ✓.
Dr. Karmach

9 · Exceptions — Chromium & Copper

Explain and apply the two building-up exceptions, Cr and Cu, where one 4s electron shifts into 3d to reach an extra-stable half-filled or filled d subshell.

Dr. Karmach

When the order bends

The building-up order predicts chromium and copper — but each atom moves one 4s electron into 3d, reaching an extra-stable half-filled or filled d subshell.

Dr. Karmach

A half-filled or filled d is extra stable

The building-up order is a reliable guide, but a few atoms do better by rearranging. Two matter for us: chromium and copper. In both, an electron leaves 4s for 3d, because a d subshell that is exactly half-filled (d⁵) or completely filled (d¹⁰) carries a small extra stability.

predicted Cr: [Ar]4s²3d⁴  →  actual: [Ar]4s¹3d⁵
one 4s electron moves to 3d · both add to 24, but only 4s¹3d⁵ is observed
Dr. Karmach

Worked example — chromium

Step 1 · Count the electrons

Cr — atomic number 24
24 electrons to place · a d-block metal in period 4

Write what the building-up order predicts, then apply the exception. After [Ar], 6 electrons remain.

Dr. Karmach

Worked example — chromium solution

Step 2 · What the order predicts

After [Ar] (18 electrons), fill 4s before 3d: 4s² then the last 4 into 3d.

predicted: [Ar]4s²3d⁴
18 + 2 + 4 = 24 · correct count, but not the ground state
Dr. Karmach

Worked example — chromium solution

Step 2 · What the order predicts

predicted: [Ar]4s²3d⁴
18 + 2 + 4 = 24 · correct count, but not the ground state
Step 3 · Apply the exception

Shift one 4s electron into 3d. Now 3d holds 5 — one electron in every d orbital, a half-filled subshell — and 4s holds 1.

actual: [Ar]4s¹3d⁵
18 + 1 + 5 = 24 ✓ · six unpaired electrons: 1 in 4s, 5 in 3d
Dr. Karmach

Worked example — chromium solution

Step 2 · What the order predicts

predicted: [Ar]4s²3d⁴
18 + 2 + 4 = 24 · correct count, but not the ground state
Step 3 · Apply the exception
actual: [Ar]4s¹3d⁵
18 + 1 + 5 = 24 ✓ · six unpaired electrons: 1 in 4s, 5 in 3d
Both forms total 24, so the count cannot flag the swap. The rule does: a half-filled 3d⁵ beats a partly filled 3d⁴.
Dr. Karmach

Copper — the same move, one shell fuller

Copper does exactly what chromium does, one step further along. The order predicts [Ar]4s²3d⁹; moving one 4s electron into 3d gives a completely filled 3d¹⁰.

predicted Cu: [Ar]4s²3d⁹  →  actual: [Ar]4s¹3d¹⁰
18 + 2 + 9 = 29 · 18 + 1 + 10 = 29 ✓ · a full d subshell, 5 × 2 = 10

The electron always comes out of 4s, not out of the core: 4s drops to 4s¹, never to 4s⁰.

Dr. Karmach

Where this goes wrong

Adding an electron instead of moving one. [Ar]4s²3d⁵ keeps 4s full — that is 25 electrons, one too many. Empty 4s to 4s¹; the electron relocates, it is not created.
Deleting the 4s electron. [Ar]3d⁵ drops 4s entirely (23, one short). It moves into 3d, it does not vanish.
Trusting the predicted form. [Ar]4s²3d⁴ has the right count, but Cr's measured ground state is [Ar]4s¹3d⁵.
Over-applying the rule. Only a nearly-half or nearly-full d borrows from 4s — V and Ni keep 4s².
Dr. Karmach

Practice — copper

Cu — atomic number 29
a d-block metal in period 4

Which is the correct ground-state configuration of copper?

  1. [Ar] 4s¹ 3d¹⁰
  2. [Ar] 4s² 3d⁹
  3. [Ar] 4s² 3d¹⁰
  4. [Ar] 4s¹ 3d⁹
Dr. Karmach

Practice — answer: A

[Ar]4s¹3d¹⁰
18 + 1 + 10 = 29 ✓ — a completely filled 3d subshell

One 4s electron shifts into 3d, filling it to 10. B is the order's prediction (18 + 2 + 9 = 29) but not the observed ground state. C keeps 4s full and fills 3d — 18 + 2 + 10 = 30, one electron too many. D leaves 3d at 9 — 18 + 1 + 9 = 28, one short.

The electron leaves 4s (down to 4s¹) and lands in 3d (up to 3d¹⁰). The total stays 29 — a move, not a change in count.
Dr. Karmach

Check yourself

  1. Write chromium's ground-state configuration, and confirm the superscripts sum to 24.
  2. Copper's [Ar]4s¹3d¹⁰ — how many unpaired electrons does it have, and why is that fewer than chromium's?

These two exceptions, Cr and Cu, are the ones to memorize for this course. Their half-filled and filled d subshells also survive into their ions, which lose the 4s electron first.

Dr. Karmach

10 · Periodic Trends

Predict which of two elements has the larger atomic radius, the higher ionization energy, or the greater electronegativity from where each sits on the periodic table.

Dr. Karmach

An atom's place predicts its size

Atoms are not all one size. Low and to the left, an atom is large; high and to the right, it is small. Position tells you which.

Dr. Karmach

Two forces set every trend

Two pulls decide every trend. Across a period, each added proton draws the same shell inward. Down a group, each new shell holds the outer electrons farther out.

Dr. Karmach

Atomic radius

Atomic radius is how far the outer electrons sit from the nucleus. It shrinks left to right as the nuclear charge climbs, and grows down a group as each new shell is added.

Dr. Karmach

Ionization energy

Ionization energy is the energy to pull one electron off a gaseous atom. A tighter grip costs more. It rises across a period and falls down a group, mirroring atomic radius.

across period 2: Li 520 → C 1086 → F 1681 kJ/mol
nuclear charge climbs, the same shell grips harder — ionization energy increases
down group 1: Li 520 → Na 496 → K 419 kJ/mol
each new shell sits farther out, easier to strip — ionization energy decreases
Dr. Karmach

Electronegativity

Electronegativity is how strongly a bonded atom pulls shared electrons toward itself. It increases across a period and up a group, peaking at fluorine. Radius runs the opposite way; ionization energy runs with it.

Dr. Karmach

The method

  1. Place the two elements. Same period, or same group?
  2. Name the trend for that direction: radius, ionization energy, or electronegativity.
  3. Apply it. State which element wins, and give the reason from nuclear charge or shells.
Dr. Karmach

Worked example 1 — sodium and sulfur

sodium (Na) and sulfur (S) — same period 3
Na: +11 nucleus · S: +16 nucleus · both fill through the n = 3 shell

Sodium sits at the left of period 3, sulfur well to its right.

Which atom has the larger atomic radius?

Dr. Karmach

Worked example 1 — solution

sodium (Na) and sulfur (S) — same period 3
Na: +11 nucleus · S: +16 nucleus · both fill through the n = 3 shell

Step 1 · Place the two elements

Sodium and sulfur share period 3, so their outer electrons occupy the same n = 3 shell. One trend decides it.

Dr. Karmach

Worked example 1 — solution

sodium (Na) and sulfur (S) — same period 3
Na: +11 nucleus · S: +16 nucleus · both fill through the n = 3 shell
Step 1 · Place the two elements Step 2 · Name the trend

Across a period, atomic radius decreases: the nuclear charge grows while the shell stays the same.

Dr. Karmach

Worked example 1 — solution

sodium (Na) and sulfur (S) — same period 3
Na: +11 nucleus · S: +16 nucleus · both fill through the n = 3 shell
Step 1 · Place the two elements Step 2 · Name the trend Step 3 · Apply it
Na vs S → sodium is larger (≈ 186 pm vs ≈ 104 pm)
same n = 3 shell · Na's +11 nucleus grips it more loosely than S's +16
Dr. Karmach

Worked example 1 — solution

sodium (Na) and sulfur (S) — same period 3
Na: +11 nucleus · S: +16 nucleus · both fill through the n = 3 shell
Step 1 · Place the two elements Step 2 · Name the trend Step 3 · Apply it
Na vs S → sodium is larger (≈ 186 pm vs ≈ 104 pm)
same n = 3 shell · Na's +11 nucleus grips it more loosely than S's +16
Sodium's shell feels the weaker pull, so it holds the same electrons farther out. Across a period, the growing nuclear charge wins.
Dr. Karmach

Worked example 2 — lithium and potassium

lithium (Li) and potassium (K) — same group 1
Li: outer electron in n = 2 · K: outer electron in n = 4

Lithium and potassium are both alkali metals, potassium two rows below.

A common first attempt: potassium holds far more protons, so its outer electron should be the hardest to remove. Which atom has the higher ionization energy?

Dr. Karmach

Worked example 2 — solution

lithium (Li) and potassium (K) — same group 1
Li: outer electron in n = 2 · K: outer electron in n = 4

A common first attempt

Potassium holds 19 protons to lithium's 3, so its grip looks stronger. But those extra protons sit buried under two extra shells. Distance and shielding, not raw charge, set the pull on the outer electron.

Dr. Karmach

Worked example 2 — solution

lithium (Li) and potassium (K) — same group 1
Li: outer electron in n = 2 · K: outer electron in n = 4
A common first attempt Step 1 · Place the two elements

Lithium and potassium share group 1. Their outer electrons sit in different shells: n = 2 for lithium, n = 4 for potassium.

Dr. Karmach

Worked example 2 — solution

lithium (Li) and potassium (K) — same group 1
Li: outer electron in n = 2 · K: outer electron in n = 4
A common first attempt Step 1 · Place the two elements Step 2 · Name the trend Step 3 · Apply it

Down a group, ionization energy decreases: each new shell holds the outer electron farther out, better shielded.

Li vs K → lithium is higher (520 vs 419 kJ/mol)
Li's n = 2 electron sits close and poorly shielded, costing the most to remove
Dr. Karmach

Worked example 2 — solution

lithium (Li) and potassium (K) — same group 1
Li: outer electron in n = 2 · K: outer electron in n = 4
A common first attempt Step 1 · Place the two elements Step 2 · Name the trend Step 3 · Apply it
Li vs K → lithium is higher (520 vs 419 kJ/mol)
Li's n = 2 electron sits close and poorly shielded, costing the most to remove
Potassium is the bigger atom, yet its electron leaves more easily. Down a group, distance beats a larger nuclear charge.
Dr. Karmach

Take-home: radius and ionization energy run opposite

down group 1: Li → Na → K, the atoms grow larger
atomic radius: 152 → 186 → 227 pm — each new shell adds size
down group 1: Li → Na → K, the electron leaves more easily
ionization energy: 520 → 496 → 419 kJ/mol — the outer electron sits farther out

The larger atom holds its outer electron more loosely. A big radius and a high ionization energy never belong to the same atom.

Dr. Karmach

Your turn — aluminum and sulfur

aluminum (Al) and sulfur (S) — same period 3
Al: +13 nucleus · S: +16 nucleus · both fill through the n = 3 shell
step question answer
1 · place them same period, or same group? same
2 · name the trend which way does radius run? radius across a period
3 · apply it which atom is larger?

Complete the three steps.

Dr. Karmach

Your turn — aluminum and sulfur

aluminum (Al) and sulfur (S) — same period 3
Al: +13 nucleus · S: +16 nucleus · both fill through the n = 3 shell
step question answer
1 · place them same period, or same group? same
2 · name the trend which way does radius run? radius across a period
3 · apply it which atom is larger?

Complete the three steps.

Al vs S → aluminum is larger
same n = 3 shell · radius decreases left to right · Al's +13 grips it less tightly than S's +16
Dr. Karmach

Where this goes wrong

Reading the trend backwards. Radius does not grow across a period. Left to right the nuclear charge climbs while the shell stays the same, so the atoms shrink. Sodium (+11) is larger than chlorine (+17), not smaller.
Mixing up across and down. Across a period, a new proton pulls the same shell tighter. Down a group, a whole new shell is added. Same period → weigh nuclear charge; same group → count the shells.
Letting more protons mean a bigger atom. Extra protons pull electrons in, never push them out. Down a group an atom grows in spite of its larger charge, because each row opens a new, higher shell.
Treating radius and ionization energy as one trend. They run opposite. The bigger atom holds its outer electron more loosely, so a large radius comes with a low ionization energy.
Dr. Karmach

Practice 1

boron (B) and oxygen (O) — same period 2
B: +5 nucleus · O: +8 nucleus · both bond through the n = 2 shell

Boron and oxygen lie in the same period. Which atom is more electronegative, and why?

  1. Boron — electronegativity falls off across a period, so the element on the left attracts shared electrons more strongly.
  2. Boron — it is the larger atom, and a larger atom pulls a bonding pair in harder.
  3. Oxygen — electronegativity increases across a period, and oxygen sits farther right, closer to fluorine.
  4. Oxygen — it has more occupied shells than boron, so it reaches shared electrons better.
Dr. Karmach

Practice 1 — answer: C

B vs O across period 2 → oxygen — answer C
B 2.0 · O 3.5 (Pauling) · both bond through n = 2, O's +8 nucleus outpulls B's +5

A ran the trend backwards: electronegativity increases, not decreases, across a period, so the right-hand atom wins. B confused the size trend: boron is the larger atom, but a larger atom pulls a shared pair less, not more. D reached for extra shells that are not there: both atoms bond through the n = 2 shell, and oxygen wins by nuclear charge, not shell count.

Across a period, electronegativity climbs toward fluorine. Oxygen, one step from it, outpulls boron. ✓
Dr. Karmach

Worked example 3 — ranking three atoms

calcium (Ca), magnesium (Mg), chlorine (Cl)
Mg & Cl: period 3 · Mg & Ca: group 2 · magnesium is the shared corner

No single row or column holds all three. Rank them by atomic radius, largest first.

Dr. Karmach

Worked example 3 — two comparisons

calcium (Ca), magnesium (Mg), chlorine (Cl)
Mg & Cl: period 3 · Mg & Ca: group 2 · magnesium is the shared corner

Step 1 · Place the two elements

Magnesium is the corner. It shares period 3 with chlorine and group 2 with calcium, so two single comparisons cover all three.

Dr. Karmach

Worked example 3 — two comparisons

calcium (Ca), magnesium (Mg), chlorine (Cl)
Mg & Cl: period 3 · Mg & Ca: group 2 · magnesium is the shared corner
Step 1 · Place the two elements Step 2 · Name the trend
Mg vs Cl (period 3): radius decreases to the right → Mg is larger
≈ 160 pm vs ≈ 99 pm · same n = 3 shell, Cl's +17 pulls harder
Across period 3, magnesium sits far to the left of chlorine, so it is the larger of the two.
Dr. Karmach

Worked example 3 — the ranking

calcium (Ca), magnesium (Mg), chlorine (Cl)
from Step 2: magnesium is larger than chlorine

Step 3 · Apply it

Mg vs Ca (group 2): radius increases downward → Ca is larger
≈ 197 pm vs ≈ 160 pm · calcium adds a shell (n = 4 vs n = 3)
Dr. Karmach

Worked example 3 — the ranking

calcium (Ca), magnesium (Mg), chlorine (Cl)
from Step 2: magnesium is larger than chlorine
Step 3 · Apply it
Mg vs Ca (group 2): radius increases downward → Ca is larger
≈ 197 pm vs ≈ 160 pm · calcium adds a shell (n = 4 vs n = 3)
largest to smallest: calcium, magnesium, chlorine
≈ 197 pm, 160 pm, 99 pm — calcium the largest, chlorine the smallest
Two clean comparisons through the shared corner rank all three, with no diagonal guesswork.
Dr. Karmach

Practice 2

fluorine (F) and iodine (I) — same group 17
F: outer electrons in n = 2 · I: outer electrons in n = 5

Fluorine and iodine are both halogens, iodine three rows lower. Which atom has the larger atomic radius, and why?

  1. Iodine — atomic radius increases down a group, and iodine's outer electrons lie in a much higher shell than fluorine's.
  2. Fluorine — atomic radius increases up a group, so the halogen nearer the top is the larger one.
  3. Iodine — iodine carries more protons, and more protons push the electron cloud outward.
  4. Fluorine — it is the more electronegative atom, and the atom that grips electrons hardest is the larger one.
Dr. Karmach

Practice 2 — answer: A

F vs I down group 17 → iodine — answer A
F ≈ 72 pm · I ≈ 133 pm · iodine's outer electrons fill through n = 5 vs fluorine's n = 2

B ran the trend backwards: radius increases down a group, not up, so the lower halogen is larger. C picked iodine for the wrong reason: extra protons pull electrons in, never out — iodine is larger because it adds whole shells. D swapped in electronegativity: fluorine does grip electrons hardest, but that tight grip marks the smaller atom, not the larger.

Down a group, each row adds a shell. Iodine, three rows below fluorine, is far the larger atom. ✓
Dr. Karmach

Check yourself

  1. Chlorine and iodine sit in the same group. Which holds its electrons more tightly, and does that make it the larger or the smaller atom?
  2. Across period 3, phosphorus lies left of chlorine. Rank their atomic radius and their ionization energy. Do the two rankings point the same way?

Electronegativity, the pull an atom keeps on shared electrons, is the trend that carries into bonding. When two bonded atoms differ in it, the shared pair sits closer to one, and the bond turns polar.

Dr. Karmach

11 · Paramagnetism & Diamagnetism

Decide whether an atom or ion is paramagnetic or diamagnetic by writing its electron configuration, filling the orbital boxes, and counting unpaired electrons.

Dr. Karmach

A magnet can sort atoms

Bring a magnet near a sample and some atoms are pulled toward it while others ignore it. The whole difference comes down to one question about the electrons — is any of them left unpaired?

Dr. Karmach

An unpaired electron is a tiny magnet

Every electron spins, and a spinning charge is a small magnet. When two electrons share an orbital, their opposite spins point the tiny magnets in opposite directions and the effect cancels. An electron with no partner has nothing to cancel it, so the whole atom keeps a net magnetic pull.

≥ 1 unpaired electron → paramagnetic — attracted to a magnet
all electrons paired → diamagnetic — weakly repelled
Dr. Karmach

Diamagnetism is the strict case

A paramagnetic species needs only a single unpaired electron. A diamagnetic one needs every electron paired — no exceptions. So the real work is counting: fill the orbital boxes and look for any lone arrow.

any lone arrow → paramagnetic
not one lone arrow anywhere → diamagnetic
Dr. Karmach

The method — count the unpaired electrons

  1. Write the configuration — for an ion, build the neutral atom, then remove the highest-n electrons.
  2. Draw the highest partly-filled sublevel as orbital boxes.
  3. Fill one per box before pairing (Hund's rule).
  4. Count the unpaired arrows — one or more → paramagnetic; none → diamagnetic.
Dr. Karmach

Worked example 1 — oxygen

Step 1 · Write the configuration

O — atomic number 8
1s²2s²2p⁴ = [He]2s²2p⁴ · 2 + 2 + 4 = 8 electrons

Oxygen is a neutral atom, so no electrons are removed. Find the highest partly-filled sublevel, fill it by Hund's rule, and count the unpaired electrons.

Dr. Karmach

Worked example 1 — solution

O — [He]2s²2p⁴
the 2p sublevel holds 4 electrons in its 3 boxes

Step 2 · Draw the partly-filled sublevel

1s and 2s are full, their electrons quietly paired. The action is all in 2p: three boxes, four electrons.

Dr. Karmach

Worked example 1 — solution

O — [He]2s²2p⁴
the 2p sublevel holds 4 electrons in its 3 boxes
Step 2 · Draw the partly-filled sublevel Step 3 · Fill by Hund's rule

One electron goes into each of the three boxes first; the fourth has no empty box left and must pair up.

2p:  ↑↓   ↑   ↑
two boxes still carry a single, unpaired electron
Dr. Karmach

Worked example 1 — solution

O — [He]2s²2p⁴
the 2p sublevel holds 4 electrons in its 3 boxes
Step 2 · Draw the partly-filled sublevel Step 3 · Fill by Hund's rule
2p:  ↑↓   ↑   ↑
two boxes still carry a single, unpaired electron
Step 4 · Count the unpaired electrons
2 unpaired → paramagnetic
a p sublevel with 4 electrons: 6 − 4 = 2 unpaired
Oxygen gas is genuinely paramagnetic. Poured between the poles of a strong magnet, pale-blue liquid O₂ hangs in the gap instead of falling through.
Dr. Karmach

Worked example 2 — the iron(III) ion

Step 1 · Write the configuration

Fe — [Ar]4s²3d⁶  →  Fe³⁺
remove 3 electrons to reach the +3 ion

A common first attempt pulls all three electrons straight out of 3d. Build Fe³⁺ the right way, then count its unpaired electrons.

Dr. Karmach

Worked example 2 — solution

A common first attempt

Stripping three electrons from 3d and leaving 4s alone:

✗ [Ar]4s²3d³
wrong order — the 4s electrons must leave before any 3d electron
Dr. Karmach

Worked example 2 — solution

A common first attempt

✗ [Ar]4s²3d³
wrong order — the 4s electrons must leave before any 3d electron
Step 1 · Remove the highest-n electrons first

Take both 4s electrons, then one 3d electron: 2 + 1 = 3 removed.

Fe³⁺: [Ar]3d⁵
26 − 3 = 23 electrons remain
Dr. Karmach

Worked example 2 — solution

A common first attempt

✗ [Ar]4s²3d³
wrong order — the 4s electrons must leave before any 3d electron
Step 1 · Remove the highest-n electrons first
Fe³⁺: [Ar]3d⁵
26 − 3 = 23 electrons remain
Steps 2–4 · Fill the boxes and count

Five electrons spread across the five 3d boxes, one apiece — not one is forced to pair.

3d:  ↑   ↑   ↑   ↑   ↑  →  5 unpaired → paramagnetic
a half-filled d sublevel carries the maximum 5 unpaired electrons
Dr. Karmach

Worked example 2 — solution

A common first attempt

✗ [Ar]4s²3d³
wrong order — the 4s electrons must leave before any 3d electron
Step 1 · Remove the highest-n electrons first
Fe³⁺: [Ar]3d⁵
26 − 3 = 23 electrons remain
Steps 2–4 · Fill the boxes and count
3d:  ↑   ↑   ↑   ↑   ↑  →  5 unpaired → paramagnetic
a half-filled d sublevel carries the maximum 5 unpaired electrons
Strip 4s before 3d. Fe²⁺ keeps that extra electron — [Ar]3d⁶, so 10 − 6 = 4 unpaired — still paramagnetic, just one fewer.
Dr. Karmach

Ions shift the count — rarely the verdict

Pulling electrons off empties the highest-n sublevel first: for a transition metal, 4s leaves before 3d. The unpaired count changes as electrons go, but as long as one stays unpaired the ion is still paramagnetic.

Fe [Ar]4s²3d⁶ · Fe²⁺ [Ar]3d⁶ · Fe³⁺ [Ar]3d⁵
4 · 4 · 5 unpaired electrons — every one paramagnetic

The verdict flips to diamagnetic only when the removal happens to leave every electron paired.

Zn [Ar]4s²3d¹⁰ → Zn²⁺ [Ar]3d¹⁰
10 − 10 = 0 unpaired either way — diamagnetic
Dr. Karmach

Where this goes wrong

Counting orbitals or total electrons instead of unpaired ones. A full 3d sublevel has 5 orbitals and 10 electrons, yet 0 are unpaired. Only the lone, unpartnered arrows decide magnetism.
Pairing electrons too early. Writing 2p⁴ as ↑↓ ↑↓ (two pairs, one empty box) gives 0 unpaired and the wrong verdict. Hund's rule fills each box singly first, so the true count is 2.
Removing (n−1)d before ns in an ion. Fe³⁺ is [Ar]3d⁵, not [Ar]4s²3d³. The 4s electrons leave first; only then does 3d give one up.
Assuming every ion is diamagnetic. Many transition-metal ions keep unpaired d electrons — Fe³⁺ has 5, Cr³⁺ has 3, both paramagnetic. Diamagnetic requires all electrons paired.
Dr. Karmach

Practice 1

Which one of these species is diamagnetic?

  1. O (oxygen atom)
  2. Fe³⁺
  3. Zn²⁺
  4. Na (sodium atom)
Dr. Karmach

Practice 1 — answer: C

Zn²⁺ = [Ar]3d¹⁰
every 3d box paired · 10 − 10 = 0 unpaired → diamagnetic

Zn²⁺ has a completely filled 3d sublevel, so no electron is left unpaired. A, oxygen, has 2 unpaired 2p electrons. B, Fe³⁺ (3d⁵), has 5 unpaired electrons. D, sodium, has a lone 3s¹ electron. All three of those are paramagnetic.

Diamagnetic is the strict verdict: not a single electron may be left unpaired.
Dr. Karmach

Practice 2

Fe²⁺: [Ar]3d⁶
the iron(II) ion — six electrons in the 3d sublevel

How many unpaired electrons does Fe²⁺ have?

  1. 6 unpaired electrons
  2. 5 unpaired electrons
  3. 4 unpaired electrons
  4. 0 unpaired electrons
Dr. Karmach

Practice 2 — answer: C

3d:  ↑↓   ↑   ↑   ↑   ↑  →  4 unpaired — answer C
6 electrons in 5 boxes: 5 go in singly, the 6th pairs · 10 − 6 = 4

A counts all six 3d electrons as if each were unpaired, ignoring the pair forced into the first box. B gives 5, the count for Fe³⁺ (3d⁵) — one electron fewer. D assumes the ion is fully paired, but six electrons cannot fill five boxes two at a time, so four stay single.

Only when a sublevel is exactly full or exactly half-empty do the arrows line up simply. Six in five boxes always leaves four unpaired.
Dr. Karmach

Check yourself

  1. Manganese is [Ar]4s²3d⁵. How many unpaired electrons does it have, and is it paramagnetic or diamagnetic?
  2. Write the configuration of Ca²⁺ and decide its magnetism.

An atom's magnetism is a direct read-out of its orbital boxes: fill them, count the lone arrows, and the verdict follows. The same unpaired-electron bookkeeping, carried into molecules and their bonding orbitals, is what explains why O₂ is magnetic while N₂ is not.

Dr. Karmach

Can you…?

  • ☐ relate a light wave's wavelength, frequency, and energy using c = λν and E = hν?
  • ☐ calculate the energy of a photon from its wavelength or frequency?
  • ☐ state how many electrons each sublevel (s, p, d, f) holds and why?
  • ☐ write the ground-state electron configuration of an atom using the building-up order?
  • ☐ predict periodic trends in atomic radius, ionization energy, and electronegativity from an element's position?

If any box stays empty, the practice site has a drill for it. 🧪

Dr. Karmach