For hydrogen like species, which of the following graphs provides the most appropriate representation of E vs Z plot for a constant n? [E: Energy of the stationary state, Z: atomic number, n: principal quantum number]

For a constant principal quantum number n, the energy E is directly proportional to -Z2. This represents a quadratic relation where the curve is a downward-opening parabola starting from the origin in the negative energy region. Since energy values are inherently negative for bound states, as Z increases, E becomes rapidly more negative following a parabolic curve. Class 11 Chemistry: Structure of Atom

For hydrogen like species, which of the following graphs provides the most appropriate representation of E vs Z plot for a constant n? [E: Energy of the stationary state, Z: atomic number, n: principa

For a constant principal quantum number n, the energy E is directly proportional to -Z2. This represents a quadratic relation where the curve is a downward-opening parabola starting from the origin in the negative energy region. Since energy values are inherently negative for bound states, as Z increases, E becomes rapidly more negative following a parabolic curve. Class 11 Chemistry: Structure of Atom

For hydrogen like species, which of the following graphs provides the most appropriate representation of E vs Z plot for a constant n? [E: Energy of the stationary state, Z: atomic number, n: principal quantum number]

For a constant principal quantum number n, the energy E is directly proportional to -Z2. This represents a quadratic relation where the curve is a downward-opening parabola starting from the origin in the negative energy region. Since energy values are inherently negative for bound states, as Z increases, E becomes rapidly more negative following a parabolic curve. Class 11 Chemistry: Structure of Atom

For hydrogen like species, which of the following graphs provides the most appropriate representation of E vs Z plot for a constant n? [E: Energy of the stationary state, Z: atomic number, n: principa

For a constant principal quantum number n, the energy E is directly proportional to -Z2. This represents a quadratic relation where the curve is a downward-opening parabola starting from the origin in the negative energy region. Since energy values are inherently negative for bound states, as Z increases, E becomes rapidly more negative following a parabolic curve. Class 11 Chemistry: Structure of Atom

For hydrogen like species, which of the following graphs provides the most appropriate representation of E vs Z plot…

Year	2026	2025	2024	Total
Questions	14	15	9	38

Q70 jee_main_2026_21_jan_morning Hydrogen Spectrum

Given below are two statements: Statement I: When an electric discharge is passed through gaseous hydrogen, the hydrogen molecules dissociate and the energetically excited hydrogen atoms produce electromagnetic radiation of discrete frequencies. Statement II: The frequency of second line of Balmer series obtained from

He⁺

is equal to that of first line of Lyman series obtained from hydrogen atom. In the light of the above statements, choose the correct answer from the options given below:

A. $Both Statement I and Statement II are true$
B. $Both Statement I and Statement II are false$
C. $Statement I is false but Statement II is true$
D. $Statement I is true but Statement II is false$

Solution

Related Formula

(1)/(λ) = RZ²((1)/(n₁²) - (1)/(n₂²))

Core Logic

Statement I is a factual description of how the hydrogen emission spectrum is obtained. Dissociation yields excited atoms that emit light at discrete frequencies. So Statement I is true.

For Statement II: First line of Lyman series for H atom ( $Z=1, n₁=1, n₂=2$ $Z=1, n_1=1, n_2=2$):

(1)/(λ₁) = R(1)²((1)/(1²) - (1)/(2²)) = R(1 - (1)/(4)) = (3R)/(4)

Second line of Balmer series for $He^+$ $He^+$ ( $Z=2, n₁=2, n₂=4$ $Z=2, n_1=2, n_2=4$):

(1)/(λ₂) = R(2)²((1)/(2²) - (1)/(4²)) = 4R((1)/(4) - (1)/(16)) = 4R((3)/(16)) = (3R)/(4)

Since $(1)/(λ₁) = (1)/(λ₂)$ , their wavelengths (and therefore frequencies) are exactly the same. Statement II is true.

Step 1: Final Conclusion

Both statements are correct.

Chapter Mix

Class 11 Chemistry: Structure of Atom

Q51 jee_main_2026_21_jan_evening Hydrogen Spectrum and Energy Levels

Consider the following spectral lines for atomic hydrogen: A. First line of Paschen series B. Second line of Balmer series C. Third line of Paschen series D. Fourth line of Bracket series The correct arrangement of the above lines in ascending order of energy is:

A. $(1) D < C < A < B$ $(1) \ D < C < A < B$
B. $(2) A < B < C < D$ $(2) \ A < B < C < D$
C. $(3) C < D < B < A$ $(3) \ C < D < B < A$
D. $(4) D < A < C < B$ $(4) \ D < A < C < B$

Solution

Related Formula

Δ E = 13.6 Z² ((1)/(n₁²) - (1)/(n₂²)) eV

Core Logic

Let's find the values of $n₁$ $n_1$ and $n₂$ $n_2$ for each transition:

(A) Paschen ( $1st$ $1^{st}$ line): $n₁ = 3, n₂ = 4$ $n_1 = 3, n_2 = 4$
(B) Balmer ( $2nd$ $2^{nd}$ line): $n₁ = 2, n₂ = 4$ $n_1 = 2, n_2 = 4$
(C) Paschen ( $3rd$ $3^{rd}$ line): $n₁ = 3, n₂ = 6$ $n_1 = 3, n_2 = 6$
(D) Bracket ( $4th$ $4^{th}$ line): $n₁ = 4, n₂ = 8$ $n_1 = 4, n_2 = 8$

Calculating or comparing the energy values corresponding to these transitions yields the ascending order of energy.

Step 1: Final Conclusion

The correct ascending order of energy of the given lines is $D < A < C < B$ $D < A < C < B$, corresponding to option (4).

Pattern Recognition

Sees: hydrogen spectral lines energy comparison. Trap: Confusing series limits with specific line numbers. Shortcut: Evaluate transition frequencies or wavelength gaps using Rydberg formula equivalents.

Chapter Mix

Class 11 Chemistry: Structure of Atom

Q54 jee_main_2026_22_january_morning Bohr Model Energy Calculations

The energy required by electrons, present in the first Bohr orbit of hydrogen atom to be excited to second Bohr orbit is ____

J mol⁻¹

. Given:

RH = 2.18 \times 10⁻¹¹ ergs

.

A. $1.635 \times 10⁻¹⁸$ $1.635 \times 10^{-18}$
B. $9.835 \times 10⁵$ $9.835 \times 10^{5}$
C. $9.835 \times 10¹²$ $9.835 \times 10^{12}$
D. $1.635 \times 10⁻¹¹$ $1.635 \times 10^{-11}$

Solution

Related Formula

Eₙ = -RH \times Z²n²

Δ E = RH Z² ( (1)/(n₁²) - (1)/(n₂²) )

Core Logic

Given $RH = 2.18 \times 10⁻¹¹ ergs$ . Convert this to Joules: $1 Joule = 10⁷ ergs RH = 2.18 \times 10⁻¹⁸ J$ .

Calculate energy difference per atom:

Δ E = 2.18 \times 10⁻¹⁸ \times 1² [ 11² - 12² ]

Δ E = 2.18 \times 10⁻¹⁸ \times ( 1 - (1)/(4) ) = 2.18 \times 10⁻¹⁸ \times (3)/(4)

Δ E = 1.635 \times 10⁻¹⁸ Joule/atom

Step 1: Conversion to per mole

To find the energy per mole, multiply by Avogadro's number ( $NA = 6.02 \times 10²³$ $N_A = 6.02 \times 10^{23}$):

Δ Emole = 1.635 \times 10⁻¹⁸ \times 6.02 \times 10²³ Joule/mole

Δ Emole = 9.84 \times 10⁵ Joule/mole \approx 9.835 \times 10⁵ J mol⁻¹

Pattern Recognition

Energy gaps in Hydrogen: $1 arrow 2$ $1 \rightarrow 2$ transition is exactly $(3)/(4)$ $\frac{3}{4}$ of the ionization energy. Watch out for per atom vs per mole unit traps.

Chapter Mix

Class 11 Chemistry: Structure of Atom

Q64 jee_main_2026_22_january_evening Balmer Series Energy Transitions

The energy of first (lowest) Balmer line of H atom is x J. The energy (in J) of second Balmer line of H atom is:

A. $x²$ $x^2$
B. $(x)/(1.35)$ $\frac{x}{1.35}$
C. $2x$ $2x$
D. $1.35x$ $1.35x$

Solution

Related Formula

Δ E = 13.6 Z² ((1)/(n₁²) - (1)/(n₂²)) eV

Core Logic

Step 1: First Balmer line ( $n₁ = 2, n₂ = 3$ $n_1 = 2, n_2 = 3$):

Δ E₁ = x = 13.6 ((1)/(2²) - (1)/(3²)) = 13.6 ((1)/(4) - (1)/(9)) = 13.6 ((5)/(36))

Step 2: Second Balmer line ( $n₁ = 2, n₂ = 4$ $n_1 = 2, n_2 = 4$):

Δ E₂ = 13.6 ((1)/(2²) - (1)/(4²)) = 13.6 ((1)/(4) - (1)/(16)) = 13.6 ((3)/(16))

Step 3: Ratio of energies:

(Δ E₂)/(x) = ((3)/(16))/((5)/(36)) = (3 \times 36)/(16 \times 5) = (27)/(20) = 1.35

Δ E₂ = 1.35 x

Pattern Recognition

Sees: Ratio of hydrogen spectrum spectral line energies. Shortcut: $(3/16) / (5/36) = 27/20 = 1.35$ $(3/16) / (5/36) = 27/20 = 1.35$.

Chapter Mix

Class 11 Chemistry: Structure of Atom Class 12 Physics: Atoms

Q51 jee_main_2026_23_january_morning Bohr Model for Hydrogen Like Species

Which of the following statements regarding the energy of the stationary state is true in the following one-electron system?

A. $-1.09 \times 10⁻¹⁸ J for second orbit of H atom.$
B. $+2.18 \times 10⁻¹⁸ J for second orbit of He⁺ ion$
C. $+8.72 \times 10⁻¹⁸ J for first orbit of He⁺ ion$
D. $-2.18 \times 10⁻¹⁸ J for third orbit of Li²⁺ ion$

Solution

Related Formula

Eₙ = -2.18 \times 10⁻¹⁸ (Z²)/(n²) J/atom

Core Logic

Evaluate the energy of the stationary state for the given species by substituting the atomic number $Z$ $Z$ and the orbit number $n$ $n$ into the energy formula for hydrogen-like species.

Step 1: Calculation for Li2+ Ion

For the $3rd$ $3^{\text{rd}}$ orbit of the $Li²⁺$ $Li^{2+}$ ion, we have $Z = 3$ $Z = 3$ (since lithium has 3 protons) and $n = 3$ $n = 3$.

E₃ = -2.18 \times 10⁻¹⁸ \times (3²)/(3²)

E₃ = -2.18 \times 10⁻¹⁸ J

Pattern Recognition

When $Z = n$ $Z = n$, the $Z²/n²$ $Z^2/n^2$ ratio becomes $1$ $1$, immediately resulting in the ground state energy of a hydrogen atom ( $-2.18 \times 10⁻¹⁸$ $-2.18 \times 10^{-18}$ J). This is a common shortcut for identifying correct energy states.

Chapter Mix

Class 11 Chemistry: Structure of Atom

For hydrogen like species, which of the following graphs provides the most appropriate representation of E vs Z plot for a constant n? [E: Energy of the stationary state, Z: atomic number, n: principal quantum number]

Solution & Explanation

Related Formula

Core Logic

Pattern Recognition

Chapter Mix

Reference Study Guides

More Structure of Atom Previous-Year Questions

Solution

Related Formula

Core Logic

Step 1: Final Conclusion

Chapter Mix

Solution

Related Formula

Core Logic

Step 1: Final Conclusion

Pattern Recognition

Chapter Mix

Solution

Related Formula

Core Logic

Step 1: Conversion to per mole

Pattern Recognition

Chapter Mix

Solution

Related Formula

Core Logic

Pattern Recognition

Chapter Mix

Solution

Related Formula

Core Logic

Step 1: Calculation for Li2+ Ion

Pattern Recognition

Chapter Mix

More Structure of Atom Questions — jee_main_2025_29_jan_evening

Select Your Target Exam

Full Mock Test Hub

Topic-wise Practice Hub

Exam Analysis Tools

Chapter Weightage & Trends

Topic-wise Practice Hub

JEE Main Exam Papers

Chapter Weightage Board

Formula Recognition

Exam Questions

Select an Exam

Welcome back