Exams › JEE Main › Chemistry › Structure of Atom
183 questions with worked solutions.
Q1. At what wavenumber does the first line of the hydrogen Balmer series occur in the atomic spectrum?
Answer: 5R / 36 cm⁻¹
Wavenumber = R(1/2^2 - 1/3^2) = R(5/36) = 5R/36. Stored 9R/400 is wrong.
Answer: Paschen series
12186.3 cm^-1 = R/9 (R=109677), so n=3 -> Paschen series. Stored Balmer (R/4 = 27419) is wrong.
Answer: 16: 9
KE ratio EX/EY = (mY lambdaY^2)/(mX lambdaX^2) = (1 x 16)/(9 x 1) = 16:9. Stored 9:1 is wrong.
Answer: 4 × 10¹
The wavelength of light can be calculated using the formula λ = (c)/(f), where c is the speed of light and f is the frequency. Plugging in the values, we find that the wavelength corresponding to a frequency of 8 × 10¹⁵ s⁻¹ is approximately 3.75 × 10⁻⁷ m, which converts to 375 nm, closest to 4 × 10¹ nm.
Answer: 1: 3√(3)
The de Broglie wavelength is inversely proportional to the momentum of a particle, which depends on its mass and velocity. Since the lithium ion has a mass 9 times that of the proton and both are accelerated through the same potential difference, the proton will have a higher velocity and thus a shorter wavelength, leading to the ratio of their wavelengths being 1: 3√3.
Answer: 4.41 × 10⁻¹⁷ J atom⁻¹
E(Li2+, n=1) = E(He+, n=1) x (3/2)^2 = 19.6e-18 x 2.25 = 4.41e-17 J/atom. The stored value 4.41e-16 is ten times too large.
Answer: h² / 32π²mₑa₀²
The kinetic energy of an electron in the Bohr model is derived from its orbital radius and the quantization of angular momentum. In the second orbit, the radius is twice that of the first, leading to the specific factor of 1/32 in the kinetic energy formula.
Answer: 1.214 × 10⁻⁷ m
DeltaE(1->2) = 2.178e-18 x 0.75 = 1.6335e-18 J; lambda = (6.62e-34 x 3e8)/1.6335e-18 = 1.214e-7 m. The stored 2.816e-7 m is wrong.
Answer: Pauli exclusion principle
The Pauli exclusion principle states that no two electrons can occupy the same quantum state within a quantum system simultaneously. In the hypothetical configuration 1s⁷, all seven electrons would be in the same 1s orbital, violating this principle.
Answer: 1.51 eV
Ground n=1, first excited n=2, second excited n=3. E3 = 13.6/9 = 1.51 eV. The stored 3.4 eV is the n=2 (first excited) value.
Answer: 9.84 × 10⁵ J mol⁻¹
Energy to go n=1 to n=2 = 1.312e6 x (1 - 1/4) = 1.312e6 x 0.75 = 9.84e5 J/mol. The stored 6.56e5 is wrong.
Answer: 8.22 × 10¹⁴ s⁻¹
The series limit of the Balmer series is the n=inf -> 2 transition: nu = R(1/2^2) = 3.29e15/4 = 8.22e14 s^-1. The stored 3.29e15 is the full R, not R/4.
Q13. What is the de Broglie wavelength associated with a car of mass 1000 kg moving at 36 km/h?
Answer: 6.626 × 10⁻³⁸ m
The de Broglie wavelength is calculated using the formula λ = (h)/(mv), where h is Planck's constant, m is the mass, and v is the velocity. For a car with a mass of 1000 kg moving at 36 km/h, the resulting wavelength is extremely small, specifically 6.626 × 10⁻³⁸ m, which reflects the negligible wave-like properties of macroscopic objects.
Answer: 6πa₀
The de Broglie wavelength of an electron in a Bohr orbit is determined by the orbit's radius and the quantization condition, which states that the circumference of the orbit must be an integer multiple of the wavelength. For the third orbit, the radius is 3 times the first orbit's radius (3a₀), leading to a wavelength of 6πa₀ when applying the de Broglie relation.
Answer: become half
The de Broglie wavelength is inversely proportional to the square root of the kinetic energy. Therefore, if the kinetic energy is increased four times, the wavelength will decrease by a factor of the square root of four, which is two, resulting in the wavelength becoming half.
Answer: 5, 0, +1/2
The correct option, 5, 0, +1/2, represents the valence electron of rubidium, which is in the fifth energy level (n=5), has an angular momentum quantum number (l) of 0 corresponding to an s orbital, and a spin quantum number of +1/2, indicating the electron's spin direction.
Answer: -e²/2r
The total energy of an electron in a circular orbit around a proton is the sum of its kinetic and potential energy. The kinetic energy is given by (1/2)mv², and the potential energy due to electrostatic attraction is -e²/r. When calculated for a stable orbit, the total energy simplifies to -e²/2r, which accounts for the balance between kinetic and potential energy.
Answer: 8.76%
The percentage of incident radiant energy transformed into kinetic energy is calculated by comparing the energy of the absorbed photons to the bond dissociation energy. The energy of the photons at the given wavelength is lower than the bond dissociation energy, resulting in a percentage of about 8.76% being converted into kinetic energy.
Answer: the repulsion between added electrons is greater than the gain in stability from attaining a noble gas arrangement
Adding a second electron to the already-negative O- ion is opposed by electron-electron repulsion that outweighs the stability gained from the noble-gas configuration (+780 kJ/mol step). That repulsion, not electronegativity, is why gaseous O2- formation is unfavourable.
Q20. Which one of the following species shows diamagnetic behavior?
Answer: H2
H2 is a diatomic molecule with paired electrons, resulting in no net magnetic moment, which is characteristic of diamagnetic substances. In contrast, the other options either have unpaired electrons or are ions that do not exhibit this behavior.
Q21. In a hydrogen atom, which statement about the relative energies of these orbitals is true?
Answer: The 3s, 3p, and 3d orbitals all possess equal energy.
For the hydrogen atom the 3s, 3p and 3d orbitals are degenerate (energy depends only on n), so option 0 is correct. The stored statement that 3s is lower than 3p holds only for multi-electron atoms.
Q22. According to Bohr's theory, the angular momentum of an electron in 5th orbit is
Answer: 2.5 h/π
Bohr's theory states that the angular momentum of an electron in a given orbit is quantized and can be calculated using the formula L = nħ, where n is the principal quantum number and ħ is the reduced Planck's constant. For the 5th orbit (n=5), the angular momentum is 5ħ, which simplifies to 2.5 h/π when considering the appropriate conversion.
Answer: 1.92 × 10^−2 m
The uncertainty in position can be calculated using the formula for uncertainty in velocity and the Heisenberg uncertainty principle. Given the velocity and its accuracy, the resulting uncertainty in position is derived to be 1.92 × 10^−2 m, making it the correct option.
Q24. Which one of the following sets of ions represents a collection of isoelectronic species?
Answer: K⁺, Cl^−, Ca²+, Sc³+
The ions K⁺, Cl^−, Ca²+, and Sc³+ all have the same number of electrons, specifically 18, making them isoelectronic. This means they share the same electron configuration, which is a key characteristic of isoelectronic species.
Q25. Which of the following sets of quantum numbers represents the highest energy of an atom?
Answer: n = 3, l = 2, m = 1, s = +1/2
By the (n+l) rule: 3s (n+l=3), 3p (4), 3d (5), 4s (4). The 3d set has the highest n+l = 5, so n=3, l=2 represents the highest-energy orbital.
Answer: 9.84 × 10⁵ J mol^−1
Ionization energy corresponds to n=1 to infinity. E(1->2) = IE*(1 - 1/2^2) = 1.312e6*0.75 = 9.84e5 J/mol.
Answer: 0.40 nm
lambda = h/(m*v) = 6.63e-34 / (1.67e-27 * 1.0e3) = 3.97e-10 m = 0.40 nm.
Answer: 1.92 × 10^−3 m
Delta_v = 600 x 0.005/100 = 0.03 m/s, so Delta_p = 9.1e-31 x 0.03 = 2.73e-32. Delta_x >= h/(4*pi*Delta_p) = 6.6e-34/(4*pi*2.73e-32) = 1.92e-3 m.
Answer: 494 nm
Energy per bond = 242000/6.02e23 = 4.02e-19 J. lambda = hc/E = (6.626e-34*3e8)/4.02e-19 = 4.95e-7 m ~ 494 nm.
Answer: −4.41 × 10^−17 J atom^−1
For one-electron ions E(n=1) is proportional to Z^2 and is negative. E(Li2+) = -(19.6e-18)*(3^2/2^2) = -19.6e-18 * 9/4 = -4.41e-17 J/atom.
Answer: n=2 to n=1
Frequency is proportional to Z^2(1/n_f^2 - 1/n_i^2). For He+ (Z=2), 4->2 gives 4*(1/4 - 1/16) = 3/4. For hydrogen, 2->1 gives (1 - 1/4) = 3/4, which is the same. So it matches the n=2 to n=1 transition.
Q32. Which of the following is the energy of a possible excited state of hydrogen?
Answer: −3.4 eV
The energy of an excited state of hydrogen corresponds to a less negative value than the ground state energy of -13.6 eV, and -3.4 eV represents the energy level of the first excited state, indicating that the electron is further from the nucleus.
Answer: 2.12 Å
The radius of the second Bohr orbit for a hydrogen atom is determined by the formula rₙ = n² * (ε₀ * h²) / (π * m * e²), where n is the principal quantum number. For n=2, this calculation results in a radius of approximately 2.12 Å, making option D the correct choice.
Answer: Linear with slope R_H
For n_i = 8 -> n_f = n, nu_bar = R_H(1/n^2 - 1/8^2). Plotting nu_bar against (1/n^2) gives a straight line of slope +R_H and intercept -R_H/64.
Answer: 9: 4
The ratio Δν̄_Lyman / Δν̄_Balmer is derived from the differences in energy levels involved in the transitions for each series. The Lyman series transitions occur from higher energy levels to n=1, while the Balmer series transitions go to n=2, resulting in a greater frequency range for the Lyman series, specifically leading to a ratio of 9:4 when calculated.
Q36. The number of orbitals associated with quantum numbers n = 5, mₛ = +1/2 is:
Answer: 25
The number of orbitals for a given principal quantum number n is calculated using the formula n². For n = 5, this results in 5² = 25 orbitals.
Q37. Which of the following is the energy of a possible excited state of hydrogen ?
Answer: -3.4 eV
The energy levels of hydrogen are quantized, and the excited states have negative energy values that are less negative than the ground state. In this case, -3.4 eV corresponds to the first excited state, indicating that the electron has absorbed energy and moved to a higher energy level.
Answer: 2.12 Å
The radius of the second Bohr orbit for a hydrogen atom is determined by the formula rₙ = n² * (h² / (4 * π² * m * e²)), where n is the principal quantum number. For n=2, this calculation yields approximately 2.12 Å, making it the correct answer.
Answer: vL/25
The series limit frequency of the Pfund series is derived from the energy levels of the hydrogen atom, specifically the transitions to the n=5 level. Since the Lyman series corresponds to transitions to n=1 and has a series limit frequency of vL, the Pfund series, which transitions to n=5, results in a frequency that is a fraction of vL, specifically vL/25.
Q40. Among the following, the energy of 2s orbital is lowest in:
Answer: K
Orbital energy scales as -13.6*Z_eff^2/n^2, so for a fixed shell (2s) the energy becomes more negative as nuclear charge rises. Among H, Li, Na, K the 2s electrons feel the greatest effective nuclear charge in K (Z=19), so 2s is lowest in energy in K.
Answer: 9: 4
For Lyman (n1=1): nu_max = R, nu_min = R(1-1/4) = 3R/4, so delta = R/4. For Balmer (n1=2): nu_max = R/4, nu_min = R(1/4-1/9) = 5R/36, so delta = R/9. Ratio = (R/4)/(R/9) = 9:4.
Q42. The region in the electromagnetic spectrum where the Balmer series lines appear is-
Answer: Visible
The Balmer series (transitions to n=2) of hydrogen falls in the visible region. (Lyman -> UV, Paschen/Brackett -> infrared.)
Q43. In the sixth period, the orbitals that are filled are
Answer: 6s, 4f, 5d, 6p
By the Aufbau order, period 6 fills the 6s, then 4f, then 5d, and finally 6p subshells. So the orbitals filled in the sixth period are 6s, 4f, 5d, 6p.
Q44. The number of orbitals associated with quantum numbers n = 5, mₛ = +1/2 is:
Answer: 25
The number of orbitals in shell n=5 is n^2 = 25. Each orbital can hold one electron with ms = +1/2, so 25 orbitals are associated with n=5, ms=+1/2.
Answer: (3) (I), (II), (III)
As wavelength decreases the Balmer lines converge to the series limit (I true); n1 = 2 for Balmer (II true); the longest-wavelength line is the 3->2 transition, n2=3 (III true). The ionization energy of hydrogen requires n1=1, so it cannot be obtained from Balmer lines (IV false). Correct set: (I), (II), (III).
Q46. The radius of the second Bohr orbit, in terms of the Bohr radius, a0, in Li2+ is:
Answer: 4a0/3
The Bohr orbit radius is r = (n^2/Z)*a0. For Li2+ (Z=3) and n=2, r = (4/3)*a0 = 4a0/3.
Q47. In which of the following pairs, the outer most electronic configuration will be the same?
Answer: Cr+ and Mn2+
Both Cr+ and Mn2+ have the same outermost electronic configuration of 3d5, as the removal of electrons from Cr and Mn leads to a similar distribution in their d orbitals.
Answer: Both statement I and statement II are true.
Rutherford's gold foil experiment primarily provided insights into the nuclear structure of the atom, but it does not address the quantized energy levels that explain the hydrogen line spectrum. Additionally, Bohr's model, while revolutionary, does not fully align with Heisenberg's uncertainty principle, which highlights the limitations of precisely knowing both position and momentum of particles.
Q49. Which of the following sets of quantum numbers is not allowed?
Answer: n = 3, ℓ = 3, m = −3, s = − 1/2
For a given n, the azimuthal quantum number l ranges 0 to n-1. With n=3, l can be 0,1,2 only, so n=3, l=3, m=-3 is not allowed.
Answer: 8.58 × 10⁻¹⁹ J
The correct option is derived from the equation E = hν, where E is the energy of the photon, h is Planck's constant, and ν is the threshold frequency. By substituting the given values, the energy calculated aligns with the minimum energy required to initiate the photoelectric effect in platinum.