(A) Both Statement I and Statement II are true
(B) Statement I is true but Statement II is false
(C) Statement I is false but Statement II is true
(D) Both Statement I and Statement II are false
Statement I describes the fundamental process of atomic emission. When high-voltage electric discharge passes through \(H_2\) gas, the molecules absorb energy and dissociate into atoms. These atoms are excited to higher energy levels. When they return to lower states, they emit radiation at specific, discrete frequencies corresponding to the energy difference between quantized orbits, forming the line spectrum.
For Statement II, we use the Rydberg formula for frequency \(\nu\): $$\nu = Rc Z^2 \left( \frac{1}{n_1^2} - \frac{1}{n_2^2} \right)$$
Case 1: Second line of Balmer series for \(\text{He}^+\)
For Balmer series, \(n_1 = 2\). The second line corresponds to the transition from \(n_2 = 4\) to \(n_1 = 2\).
For \(\text{He}^+\), \(Z = 2\).
$$\nu_{He^+} = Rc (2)^2 \left( \frac{1}{2^2} - \frac{1}{4^2} \right)$$
$$\nu_{He^+} = 4Rc \left( \frac{1}{4} - \frac{1}{16} \right) = 4Rc \left( \frac{4-1}{16} \right) = 4Rc \left( \frac{3}{16} \right) = \frac{3}{4}Rc$$
Case 2: First line of Lyman series for Hydrogen
For Lyman series, \(n_1 = 1\). The first line corresponds to the transition from \(n_2 = 2\) to \(n_1 = 1\).
For \(H\), \(Z = 1\).
$$\nu_{H} = Rc (1)^2 \left( \frac{1}{1^2} - \frac{1}{2^2} \right)$$
$$\nu_{H} = Rc \left( 1 - \frac{1}{4} \right) = \frac{3}{4}Rc$$
Since \(\nu_{He^+} = \nu_{H}\), Statement II is True.
The study of atomic spectra provided the first evidence that energy in atoms is quantized. When an element in the gaseous state is heated or subjected to an electric discharge, it emits light. If this light is passed through a prism, it does not produce a continuous rainbow (like white light) but rather a series of sharp, isolated lines. This is known as a line emission spectrum. Each element has a unique "fingerprint" spectrum.
In the case of Hydrogen, the simplest atom, the spectrum consists of several series of lines named after their discoverers: Lyman, Balmer, Paschen, Brackett, and Pfund. The discrete nature of these lines was inexplicable by classical physics, which predicted that an electron orbiting a nucleus should lose energy continuously and eventually spiral into the nucleus.
Niels Bohr solved this by postulating that electrons revolve in stationary orbits of fixed energy. Energy is only emitted or absorbed when an electron "jumps" from one orbit to another. The energy of an electron in the \(n^{th}\) orbit is given by: $$E_n = -2.18 \times 10^{-18} \left( \frac{Z^2}{n^2} \right) \text{ Joules}$$ This equation shows that as \(n\) increases, the energy becomes less negative (higher energy). The negative sign indicates that the electron is bound to the nucleus.
Johannes Rydberg generalized the observations of Balmer into a mathematical formula that predicts the wavelength (\(\lambda\)) or wave number (\(\bar{\nu}\)) of any line in the hydrogen spectrum: $$\bar{\nu} = \frac{1}{\lambda} = R_H Z^2 \left( \frac{1}{n_1^2} - \frac{1}{n_2^2} \right)$$ Where \(R_H\) is the Rydberg constant (\(\approx 1.09677 \times 10^7 \text{ m}^{-1}\)). To find frequency (\(\nu\)), we use \(\nu = c / \lambda\).
| Series | \(n_1\) (Lower) | \(n_2\) (Higher) | Spectral Region |
|---|---|---|---|
| Lyman | 1 | 2, 3, 4... | Ultraviolet |
| Balmer | 2 | 3, 4, 5... | Visible |
| Paschen | 3 | 4, 5, 6... | Infrared |
| Brackett | 4 | 5, 6, 7... | Infrared |
Bohr's theory applies to "Hydrogen-like" species—ions containing only one electron, such as \(\text{He}^+, \text{Li}^{2+}, \text{Be}^{3+}\). The key difference is the atomic number \(Z\). Since the frequency is proportional to \(Z^2\), an ion with \(Z=2\) will have frequencies four times higher than hydrogen for the same transition transitions.
To find if two transitions in different species have the same frequency, check if the value of \(Z^2 \left( \frac{1}{n_1^2} - \frac{1}{n_2^2} \right)\) is identical. For example, a transition from \(n=4 \to n=2\) in \(\text{He}^+\) (\(Z=2\)) yields: $$2^2 \left( \frac{1}{2^2} - \frac{1}{4^2} \right) = 4 \left( \frac{1}{4} - \frac{1}{16} \right) = 1 - \frac{1}{4} = \frac{3}{4}$$ This matches the \(n=2 \to n=1\) transition in Hydrogen (\(Z=1\)): $$1^2 \left( \frac{1}{1^2} - \frac{1}{2^2} \right) = \frac{3}{4}$$
While Bohr's model explains the line spectrum, it fails to explain the relative intensities of the lines or the "fine structure" (splitting of lines). This required the development of wave mechanics (Schrödinger equation), which replaces fixed orbits with "orbitals"—regions of probability. However, for calculating frequencies of 1-electron systems, Bohr's results remain perfectly accurate.
The "limiting line" or "series limit" of any series occurs when the electron transitions from \(n_2 = \infty\) to the base orbit \(n_1\). This radiation represents the ionization energy if starting from the ground state. For the Lyman series limit: $$\bar{\nu}_{limit} = R_H \left( \frac{1}{1^2} - \frac{1}{\infty} \right) = R_H$$
This topic is a cornerstone of Physics and Chemistry in JEE and NEET. Questions often involve: 1. Calculating the number of spectral lines emitted when an electron drops from a high orbit to ground state: \(\text{Lines} = \frac{n(n-1)}{2}\). 2. Comparing wavelengths and frequencies across different H-like ions. 3. Identifying the region of the electromagnetic spectrum (UV, Visible, IR).
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