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Exercises · 12.10

Q.A 12.5 eV12.5\ \text{eV} electron beam is used to bombard gaseous hydrogen at room temperature. What series of wavelengths will be emitted?

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A 12.5 eV electron beam can supply enough energy to excite ground-state hydrogen atoms up to n=3n=3 (which needs 12.09 eV) but not to n=4n=4 (which needs 12.75 eV). The excited atoms then de-excite via three possible downward jumps — 3→23\to2, 3→13\to1, and 2→12\to1 — emitting three distinct wavelengths: two in the Lyman series (102.6 nm102.6\ \text{nm} and 121.5 nm121.5\ \text{nm}) and one in the Balmer series (656.3 nm656.3\ \text{nm}).


Why the Bohr model is the right tool

At room temperature, essentially all hydrogen atoms sit in the ground state (n=1n=1). When the 12.5 eV electron beam collides with these atoms, a beam electron can transfer some of its kinetic energy to the bound atomic electron — but only in the exact discrete amounts that match the gap between two Bohr energy levels. If the beam energy is short of the next gap, no excitation happens (the collision is elastic). So the first job is to find which excited levels are actually reachable.

The hydrogen energy levels are:

En=−13.6 eVn2E_n = -\frac{13.6\ \text{eV}}{n^2}

Step 1 — Which levels can 12.5 eV reach?

Ground state: E1=−13.6 eVE_1 = -13.6\ \text{eV}.

ΔE1→2=E2−E1=(−13.64)−(−13.6)=10.2 eV\Delta E_{1\to2} = E_2 - E_1 = \left(-\frac{13.6}{4}\right) - (-13.6) = 10.2\ \text{eV}

ΔE1→3=E3−E1=(−13.69)−(−13.6)≈12.09 eV\Delta E_{1\to3} = E_3 - E_1 = \left(-\frac{13.6}{9}\right) - (-13.6) \approx 12.09\ \text{eV}

ΔE1→4=E4−E1=(−13.616)−(−13.6)=12.75 eV\Delta E_{1\to4} = E_4 - E_1 = \left(-\frac{13.6}{16}\right) - (-13.6) = 12.75\ \text{eV}

The 12.5 eV beam can supply 10.2 eV10.2\ \text{eV} (reaching n=2n=2) and 12.09 eV12.09\ \text{eV} (reaching n=3n=3), but not 12.75 eV12.75\ \text{eV} (reaching n=4n=4). So the highest level any atom can be excited to is n=3n=3; the beam electron that caused a 1→31\to3 excitation keeps the leftover 12.5−12.09=0.41 eV12.5 - 12.09 = 0.41\ \text{eV} as its own kinetic energy — the atom only ever absorbs a whole discrete quantum, never a fraction.

Step 2 — List every allowed downward transition

Some atoms end up excited to n=2n=2, some to n=3n=3. Each can then fall to any lower level:

  • From n=3n=3: 3→23\to2 and 3→13\to1
  • From n=2n=2: 2→12\to1

That gives three distinct spectral lines in total (an atom excited to n=3n=3 may cascade 3→2→13\to2\to1, emitting two photons, or jump directly 3→13\to1, emitting one — across many atoms, all three lines appear).

Step 3 — Compute each wavelength

Using the Rydberg relation 1λ=R(1nf2−1ni2)\dfrac{1}{\lambda} = R\left(\dfrac{1}{n_f^2} - \dfrac{1}{n_i^2}\right) with R=1.097×107 m−1R = 1.097 \times 10^7\ \text{m}^{-1}:

3→13\to1 (Lyman):

1λ=R(1−19)=8R9  ⇒  λ=98R≈1.026×10−7 m=102.6 nm\frac{1}{\lambda} = R\left(1 - \frac{1}{9}\right) = \frac{8R}{9} \;\Rightarrow\; \lambda = \frac{9}{8R} \approx 1.026\times10^{-7}\ \text{m} = 102.6\ \text{nm}

2→12\to1 (Lyman): …

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