Intuition Why a whole page of examples?
The parent note gave you two headline formulas and three tidy examples. But an exam does not hand you a tidy case — it hands you a weird one: a heavy ion, an absorption instead of emission, a "find the wavelength" wrapped inside a "find the speed", or the sneaky "n → ∞ " limit. This page walks every kind of question the Bohr model can produce, so no scenario ever surprises you.
We only ever use the four facts the parent built:
r n = 0.529 Z n 2 A ˚ (radius grows with n 2 , shrinks with Z )
E n = − 13.6 n 2 Z 2 eV (energy negative, rises toward 0 )
v n = 2.18 × 1 0 6 n Z m/s (speed grows with Z , shrinks with n )
ν ˉ = λ 1 = R H Z 2 ( n 1 2 1 − n 2 2 1 ) , R H = 1.097 × 1 0 7 m − 1
One conversion we lean on all page: == 1 A ˚ = 1 × 1 0 − 10 m == (an ångström is a ten-billionth of a metre — atomic-orbit sized).
Every Bohr problem is one (or a combination) of the cells below. Each worked example is tagged with the cell it lands in.
#
Case class
The twist it tests
Example
A
Radius, plain
n 2 / Z scaling
Ex 1
B
Energy, plain
negative sign, Z 2 / n 2
Ex 2
C
Emission (jump down )
Δ E > 0 released as light
Ex 3
D
Absorption (jump up )
electron must swallow a photon
Ex 4
E
Ionisation (n 2 = ∞ )
the n → ∞ limit
Ex 5
F
Speed & period
using v n , geometry of the orbit
Ex 6
G
Hydrogen-like scaling trap
"same energy, different atom" coincidence
Ex 7
H
Degenerate / limiting inputs
n = 1 floor, Z = 1 , n → ∞
Ex 8
I
Real-world word problem
series limit / colour of light
Ex 9
J
Exam twist (reverse)
given the answer, find n or Z
Ex 10
The single picture below is the map of the whole matrix : every spectral cell (C, D, E) is one of the coloured arrows on a hydrogen energy staircase. Keep glancing back at it as you read Ex 3, 4 and 5 — the red arrow is Ex 3's kind of jump, the blue arrow is Ex 4's, the yellow arrow is Ex 5's.
Each rung is an allowed energy E n ; the dashed green line at the top (E = 0 ) is the "free electron" ceiling. Down = emit light, up = absorb light, all the way to the top = ionise. That one diagram organises half the examples on this page.
Recall Sign convention we never break
Emitted photon energy ::: Δ E = E high − E low > 0 (a positive amount of light leaves the atom).
Absorbed photon energy ::: same size, but the electron gains it and climbs up.
Worked example 1. Radius of the
n = 4 orbit of He +
Statement: He + has Z = 2 . Find r 4 .
Forecast: Guess before computing — is r 4 bigger or smaller than the Bohr radius 0.529 Å? (Hint: n = 4 pushes it out, Z = 2 pulls it in.)
Write the ratio n 2 / Z = 4 2 /2 = 16/2 = 8 .
Why this step? The whole formula is just 0.529 Å times this dimensionless number — so nail the number first.
Multiply: r 4 = 0.529 × 8 = 4.232 Å.
Why this step? Direct substitution into r n = 0.529 ( n 2 / Z ) .
Verify: 8 > 1 , so the orbit is 8 × the ground-state hydrogen orbit — bigger, as forecast. The n 2 = 16 growth beat the Z = 2 shrink. Look at figure s02: the He + n = 4 ring (blue, outermost) dwarfs the ground-state hydrogen ring (yellow). Units: Å (length) ✓.
Worked example 2. Energy of the
n = 3 orbit of Li 2 +
Statement: Li 2 + has Z = 3 . Find E 3 in eV.
Forecast: Will the answer be positive or negative? (Every bound electron sits below zero.)
Ratio Z 2 / n 2 = 3 2 / 3 2 = 9/9 = 1 .
Why this step? Get the dimensionless multiplier before touching − 13.6 .
E 3 = − 13.6 × 1 = − 13.6 eV.
Why this step? Substitute into E n = − 13.6 ( Z 2 / n 2 ) ; the minus sign is mandatory (bound = negative).
Verify: − 13.6 eV is exactly the ground-state energy of hydrogen — a coincidence from Z 2 = n 2 = 9 . Negative sign present ✓, magnitude reasonable (few eV to few tens of eV) ✓.
Worked example 3. Emission energy for
He + falling n 2 = 3 → n 1 = 2
Statement: An electron in He + (Z = 2 ) drops from n = 3 to n = 2 . How much energy is released, in eV? (This is the red-arrow kind of jump in figure s01.)
Forecast: The electron falls into a deeper well, so it must lose energy — that lost energy leaves as a photon. Answer should be positive.
Start from the raw energies (each carries its own minus sign):
Δ E = E n 2 − E n 1 = ( − 13.6 n 2 2 Z 2 ) − ( − 13.6 n 1 2 Z 2 ) .
Why this step? Emission energy = energy of the higher level minus the lower level. Both are negative, so we must track the signs carefully.
Distribute the outer minus onto the second bracket (a minus times a minus becomes plus):
Δ E = − 13.6 n 2 2 Z 2 + 13.6 n 1 2 Z 2 = 13.6 Z 2 ( n 1 2 1 − n 2 2 1 ) .
Why this step? This is exactly how the two negative signs cancel into the familiar positive form: the second term flips to + , and factoring out 13.6 Z 2 leaves the 1/ n 1 2 − 1/ n 2 2 bracket. Writing small n first keeps the bracket positive for a downward jump.
Bracket: 2 2 1 − 3 2 1 = 4 1 − 9 1 = 36 9 − 4 = 36 5 .
Why this step? Common denominator 36 keeps it exact before we decimalise.
Δ E = 13.6 × 4 × 36 5 = 13.6 × 36 20 = 7.556 eV.
Why this step? Z 2 = 2 2 = 4 ; multiply everything through.
Verify: Positive ✓ (energy released, as forecast). For hydrogen the same jump gives only 13.6 × 5/36 = 1.889 eV; the Z 2 = 4 boost makes He + emit exactly 4 × more — internally consistent ✓.
10.0 eV photon lift ground-state hydrogen to n = 2 ?
Statement: Hydrogen (Z = 1 ) sits in n = 1 . A photon of 10.0 eV arrives. Does the electron reach n = 2 ? (This is the blue-arrow kind of jump in figure s01.)
Forecast: Absorption is emission run backwards — the electron must swallow exactly the gap E 2 − E 1 . Guess: is 10.0 eV enough, too little, or too much?
E 1 = − 13.6 eV, E 2 = − 13.6/4 = − 3.4 eV.
Why this step? We need the two levels' energies to size the gap.
Gap = E 2 − E 1 = − 3.4 − ( − 13.6 ) = 10.2 eV.
Why this step? Absorption needs a photon of exactly this energy — atoms are picky, unlike a ramp.
Compare: 10.0 < 10.2 . The photon is too small ; the electron stays in n = 1 .
Why this step? Bohr allows only exact matches. 10.0 eV lands between steps, which is forbidden — the photon passes straight through.
Verify: Gap 10.2 eV is the famous Lyman-α absorption of hydrogen ✓. The photon must match to ± 0 (no partial climbs), so 10.0 = 10.2 ⇒ no transition ✓.
Worked example 5. Energy to fully ionise
He + from its ground state
Statement: Remove the electron from He + (Z = 2 , starting n = 1 ) all the way to freedom. (This is the yellow-arrow all-the-way-to-the-top jump in figure s01.)
Forecast: "Free" means n → ∞ , where E ∞ = 0 . So ionisation energy = 0 − E 1 = ∣ E 1 ∣ . It should be bigger than hydrogen's 13.6 eV because Z is larger.
E 1 = − 13.6 1 2 Z 2 = − 13.6 × 4 = − 54.4 eV.
Why this step? The starting level sets the depth of the well.
As n → ∞ , n 2 1 → 0 , so E ∞ = − 13.6 Z 2 ⋅ 0 = 0 .
Why this step? This is the limiting case — the "top of the staircase" where the electron is unbound.
Ionisation energy = E ∞ − E 1 = 0 − ( − 54.4 ) = 54.4 eV.
Why this step? Energy needed = final minus initial; a positive input because we fight the attraction.
Verify: 54.4 = 4 × 13.6 ✓ — the Z 2 = 4 scaling. Positive (we supply energy) ✓. This is why He + is much harder to ionise than H (Ionisation energy ).
Worked example 6. Speed and time-per-revolution of the electron in
n = 1 hydrogen
Statement: For H (Z = 1 , n = 1 ) find the orbital speed v 1 and the period T (time for one full loop). Use the Bohr radius r 1 = 0.529 Å.
Forecast: The circumference is tiny and the speed is huge (∼ 1 0 6 m/s), so the period should be extremely short — femtoseconds?
v 1 = 2.18 × 1 0 6 n Z = 2.18 × 1 0 6 1 1 = 2.18 × 1 0 6 m/s.
Why this step? Straight from the speed formula the parent gave.
Convert the radius to metres first: since 1 A ˚ = 1 × 1 0 − 10 m, r 1 = 0.529 A ˚ = 0.529 × 1 0 − 10 m.
Why this step? Speed is in metres per second, so the length must be in metres too — otherwise the units won't cancel. This is the ångström conversion stated at the top of the page.
Circumference C = 2 π r 1 = 2 π ( 0.529 × 1 0 − 10 ) = 3.324 × 1 0 − 10 m.
Why this step? Period is "distance around one loop ÷ speed", and the loop's length is its circumference (see figure s03, where the arrow traces one full lap).
T = v 1 C = 2.18 × 1 0 6 3.324 × 1 0 − 10 = 1.525 × 1 0 − 16 s.
Why this step? Uniform circular motion: time = distance ÷ speed.
Verify: T ≈ 1.5 × 1 0 − 16 s = 0.15 fs — femtosecond scale, matching the forecast that the electron laps the nucleus millions of billions of times per second ✓. Units: m ÷ (m/s) = s ✓.
Worked example 7. Which orbit of
Be 3 + has the same energy as ground-state hydrogen?
Statement: Hydrogen's ground state is − 13.6 eV. Be 3 + has Z = 4 . Find the n for which Be 3 + matches − 13.6 eV.
Forecast: Energy ∝ Z 2 / n 2 . To keep Z 2 / n 2 = 1 we need n = Z . So guess n = 4 .
Set E n ( Be 3 + ) = − 13.6 : − 13.6 n 2 Z 2 = − 13.6 .
Why this step? Equate the target energy to the formula and solve for n .
Divide out − 13.6 : n 2 Z 2 = 1 ⇒ n = Z = 4 .
Why this step? Only the ratio matters; n must equal Z for the constant to be 1 .
Verify: E 4 ( Be 3 + ) = − 13.6 × 16/16 = − 13.6 eV ✓. This is the general rule: the n = Z orbit of any hydrogen-like ion always sits at − 13.6 eV — the trap that fools students into thinking heavy ions have "hydrogen-like" energies everywhere (Quantum mechanical model of atom explains why this exactness breaks for real multi-electron atoms).
Worked example 8. The three edge cases:
n = 1 floor, Z = 1 baseline, n → ∞ ceiling (hydrogen)
Statement: For hydrogen (Z = 1 ), state r 1 , E 1 , and both limits as n → ∞ : r ∞ and E ∞ .
Forecast: The staircase has a lowest step (n = 1 , cannot go lower) and an infinitely high top (n → ∞ ) where the electron floats free. Radius should blow up; energy should climb to 0 .
Floor: r 1 = 0.529 1 1 = 0.529 Å, E 1 = − 13.6 1 1 = − 13.6 eV.
Why this step? n = 1 is the smallest allowed integer — there is no n = 0 (that would put the electron on the nucleus, forbidden).
Radius ceiling: as n → ∞ , r n = 0.529 n 2 → ∞ .
Why this step? The n 2 growth is unbounded — the electron drifts arbitrarily far out.
Energy ceiling: as n → ∞ , E n = − 13.6/ n 2 → 0 − .
Why this step? 1/ n 2 → 0 , so the energy approaches zero from below — the electron becomes just barely free.
Verify: r ∞ = ∞ and E ∞ = 0 are consistent: infinitely far apart means no attraction energy left ✓. There is no allowed state below n = 1 , which is exactly why hydrogen is stable and doesn't collapse — the point of Bohr's whole model (Rutherford model lacked this floor).
Worked example 9. What colour is the shortest-wavelength line of the hydrogen Lyman series?
Statement: The Lyman series is every jump down to n 1 = 1 . Its series limit (shortest wavelength) comes from n 2 → ∞ . Find that wavelength (H, Z = 1 ) and say which part of the spectrum it lies in.
Forecast: The biggest possible drop into n = 1 gives the most energetic photon ⇒ the shortest wavelength. To n = 1 the gaps are large (10–13.6 eV), so this is well beyond visible — ultraviolet.
ν ˉ = R H Z 2 ( 1 2 1 − ∞ 2 1 ) = R H ( 1 − 0 ) = R H = 1.097 × 1 0 7 m⁻¹.
Why this step? n 2 → ∞ kills the second term — the limiting (maximum) wavenumber.
λ = ν ˉ 1 = 1.097 × 1 0 7 1 = 9.116 × 1 0 − 8 m = 91.2 nm.
Why this step? Wavelength is the reciprocal of wavenumber.
91.2 nm is far below the 400 –700 nm visible band ⇒ ultraviolet .
Why this step? Compare to the human-visible window to name the region.
Verify: 91.2 nm is the accepted Lyman limit of hydrogen ✓. It is shorter than the Balmer-α red line (656 nm from the parent note), as forecast — deeper falls make bluer/UV light (Hydrogen spectrum & Rydberg formula ).
Worked example 10. A hydrogen electron emits a
12.09 eV photon landing in n = 1 . Where did it start?
Statement: Emission photon = 12.09 eV, final level n 1 = 1 , hydrogen (Z = 1 ). Find the initial level n 2 .
Forecast: 12.09 eV is close to the 13.6 eV ionisation energy, so the electron fell from high up — probably n 2 = 3 .
Δ E = 13.6 ( 1 2 1 − n 2 2 1 ) = 12.09 .
Why this step? Reverse the emission formula: we know the energy, we solve for the unknown level.
1 − n 2 2 1 = 13.6 12.09 = 0.889 ⇒ n 2 2 1 = 0.111 = 9 1 .
Why this step? Isolate 1/ n 2 2 ; recognising 0.111 = 1/9 gives a clean integer.
n 2 2 = 9 ⇒ n 2 = 3 .
Why this step? Take the positive root (n is a positive integer).
Verify: Check forward: 13.6 ( 1 − 1/9 ) = 13.6 × 8/9 = 12.09 eV ✓. Matches the forecast n 2 = 3 ; this is the Lyman-β line ✓.
Common mistake "For absorption I subtract the small
n from the big n to get a negative photon energy."
Why it feels right: absorption is "going up", so it feels like the energy should be signed differently. Fix: a photon's energy is always a positive number. For absorption the electron gains the gap E high − E low > 0 ; for emission it loses the same positive amount. The direction (up/down) is a property of the electron, not a minus sign on the photon (see Ex 3 vs Ex 4).
Common mistake "Ionisation energy of
He + is 13.6 eV like hydrogen."
Why it feels right: we memorise 13.6 eV as "the ionisation energy." Fix: that 13.6 eV is only for Z = 1 , n = 1 . Ionisation energy scales as Z 2 : He + needs 54.4 eV (Ex 5), Li 2 + needs 122.4 eV.
Recall One-line summary of the matrix
Radius/energy questions ::: plug the dimensionless ratio n 2 / Z (into 0.529 Å) or Z 2 / n 2 (into − 13.6 eV) — cells A, B.
Spectral questions ::: emission = drop released as light, absorption = exact gap swallowed, ionisation = jump to n = ∞ — cells C, D, E.
Reverse questions ::: set the formula equal to the given number and solve for n or Z — cells G, J.
Hinglish version of the parent
Hydrogen spectrum & Rydberg formula — cells C, D, E, I feed directly into this.
Ionisation energy — cell E is literally its definition for hydrogen-like ions.
Quantum mechanical model of atom — explains why cell G's exactness fails for real atoms.
Rutherford model — cell H's stable floor is the fix Bohr added.
plug n2 over Z or Z2 over n2
set formula equal find n or Z