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What are \(E\) and \(L\) (as a multiple of \(\hbar\) ) of a hydrogen atom in the \(6 f\) state?

Short Answer

Expert verified
The energy level \(E\) of a hydrogen atom in the \(6f\) state is -0.378 eV and the orbital angular momentum \(L\) is \(2 \sqrt{3} \, \hbar\).

Step by step solution

01

Determination of the principal quantum number \(n\) and the azimuthal quantum number \(l\)

From the given \(6f\) state, it can be inferred that \(n = 6\) and \(l = 3\) (since the f orbital corresponds to \(l = 3\)).
02

Calculation of the energy level \(E\)

Substitute \(n = 6\) into the formula \(E_n = - \frac{{13.6 \, \text{eV}}}{n^2}\) to find the energy associated with the electron in the \(6f\) state: \(E_n = - \frac{{13.6 \, \text{eV}}}{6^2} = - \frac{{13.6 \, \text{eV}}}{36} = -0.378 \, \text{eV}\). Thus, the energy level \(E\) for a hydrogen atom in the \(6f\) state is -0.378 eV.
03

Calculation of the orbital angular momentum \(L\)

Substitute \(l = 3\) into the formula \(L = \sqrt{l(l + 1)} \, \hbar\) to find the orbital angular momentum. \[L = \sqrt{3(3 + 1)} \, \hbar = \sqrt{12} \, \hbar = 2 \sqrt{3} \, \hbar\]. Therefore, the orbital angular momentum \(L\) for a hydrogen atom in the \(6f\) state is \(2 \sqrt{3} \, \hbar\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Principal Quantum Number
The principal quantum number, denoted by \( n \), plays a crucial role in quantum mechanics, particularly in defining the discrete energy levels of an atom. It is a positive integer \((n = 1, 2, 3, \ldots)\) that indicates the main energy level occupied by an electron. This number corresponds to the electron shell, which can be thought of as how far the electron is from the nucleus on average. For the hydrogen atom, the principal quantum number determines the energy associated with each state.
This is because the energy of an electron in the hydrogen atom depends on the formula \( E_n = - \frac{{13.6 \, \text{eV}}}{n^2} \).
As \(n\) increases, the electron occupies an orbital that is farther away from the nucleus, leading to higher energy and weaker attraction to the nucleus. This sequential energy increase outlines the hierarchical order of electron states within an atom, moving from low energy close to the nucleus to high energy farther away.
Azimuthal Quantum Number
The azimuthal quantum number is denoted by \( l \) and is integral in describing the shape and type of orbital an electron occupies. Also known as the angular momentum quantum number, \( l \) can have values from \(0\) to \(n-1\).
For every value of \(n\), there are \(n\) types of orbitals, indicated by \( l \):
  • \(l = 0\) corresponds to the "s" orbital.
  • \(l = 1\) to the "p" orbital.
  • \(l = 2\) to the "d" orbital.
  • \(l = 3\) to the "f" orbital, and so forth.
The azimuthal quantum number, therefore, not only defines the shape of an electron's probability cloud but is also linked to the orbital angular momentum of electrons. It stands as a pivotal parameter in quantum chemistry, signifying how the electron cloud is distributed in the space around the nucleus.
In the given exercise, the state \(6f\) associates \( n = 6 \) with \( l = 3 \), implying a more complex "f" orbital.
Orbital Angular Momentum
Orbital angular momentum is a fundamental property in quantum mechanics, providing insights into how an electron moves within its orbit. It is quantified by the azimuthal quantum number \( l \). The formula \( L = \sqrt{l(l + 1)} \, \hbar \) is used to calculate the orbital angular momentum of an electron.
In this equation, \( \hbar \) is the reduced Planck's constant, a key constant in quantum physics. The term \( l(l + 1) \) stems from the quantum mechanical solution of the angular part of the Schrödinger equation in spherical coordinates.
This formula shows that angular momentum, unlike other assigned numerical quantum states, is not just an integer but depends on the square root of a range specified by \( l \).
In the \(6f\) state of a hydrogen atom, where \( l = 3 \), the angular momentum \( L \) is calculated as \(2\sqrt{3} \, \hbar\), demonstrating the electron's motion and distribution within its orbital.
Energy Levels in Hydrogen Atom
The concept of energy levels in the hydrogen atom is foundational in atomic physics. They are quantized, meaning that electrons can only occupy certain allowed energy levels, characterized primarily by the principal quantum number \( n \). This quantization leads to discrete energy states that electrons can transition between, emitting or absorbing photons with energy corresponding to the difference between these levels.
The energy level for any given principal quantum number is calculated using the formula \( E_n = - \frac{13.6 \, \text{eV}}{n^2} \). This equation shows that with the increase in \( n \), the binding energy becomes less negative (closer to zero), implying that higher energy levels are less tightly bound to the nucleus.
In the \(6f\) state, \( n = 6 \) and the associated energy \( E \) is \(-0.378 \, \text{eV}\). This energy value signifies that the electron is relatively far from the nucleus and requires less energy to be ionized,
exemplifying how higher energy levels have weaker attractive forces in the hydrogen atom.

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Most popular questions from this chapter

In general, an atom can have both orbital angular momentum and spin angular momentum. The total angular momentum is defined to be \(\vec{J}=\vec{L}+\vec{S} .\) The total angular momentum is quantized in the same way as \(\vec{L}\) and \(\vec{S}\). That is, \(J=\sqrt{j(j+1)} \hbar\), where \(j\) is the total angular momentum quantum number. The z-component of \(\vec{J}\) is \(J_{z}=L_{z}+S_{z}=m_{j} \hbar,\) where \(m_{j}\) goes in integer steps from \(-j\) to \(+j .\) Consider a hydrogen atom in a \(p\) state, with \(l=1\). a. \(L_{\mathrm{z}}\) has three possible values and \(S_{\mathrm{r}}\) has two. List all possible combinations of \(L_{z}\) and \(S_{z} .\) For each, compute \(J_{z}\) and determine the quantum number \(m_{j} .\) Put your results in a table. b. The number of values of \(J_{\varepsilon}\) that you found in part a is too many to go with a single value of \(j .\) But you should be able to divide the values of \(J_{z}\) into two groups that correspond to two values of \(j .\) What are the allowed values of \(j ?\) Explain. In a classical atom, there would be no restrictions on how the two angular momenta \(\vec{L}\) and \(\vec{S}\) can combine. Quantum mechanics is different. You've now shown that there are only two allowed ways to add these two angular momenta.

What is the angular momentum of a hydrogen atom in (a) a \(4 p\) state and (b) a \(5 f\) state? Give your answers as a multiple of \(\hbar\).

List the quantum numbers, excluding spin, of (a) all possible \(3 p\) states and (b) all possible \(3 d\) states.

\(1.0 \times 10^{6}\) atoms are excited to an upper energy level at \(t=0\) s. At the end of 20 ns, \(90 \%\) of these atoms have undergone a quantum jump to the ground state. a. How many photons have been emitted? b. What is the lifetime of the excited state?

A 1.0 mW helium neon laser emits a visible laser beam with a wavelength of 633 nm. How many photons are emitted per second?

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