P Chem 2 8A Hydrogenic Atoms

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66 Terms

1

What are spectral lines in a hydrogen atom?

Spectral lines in a hydrogen atom occur when electrons transition between energy levels, releasing or absorbing energy as light of specific wavelengths.

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2

What does the Rydberg constant represent conceptually?

The Rydberg constant is a value that relates to the wavelengths of light emitted or absorbed by an electron transitioning between energy levels in a hydrogen atom.

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3

What is the difference between the Lyman, Balmer, and Paschen series in the hydrogen atom?

The Lyman series involves transitions to the lowest energy level (n=1) and emits ultraviolet light. The Balmer series involves transitions to the second energy level (n=2) and emits visible light. The Paschen series involves transitions to the third energy level (n=3) and emits infrared light.

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4

What is a hydrogenic atom?

A hydrogenic atom is any atom or ion that has only one electron, similar to hydrogen, but it can have more than one proton in its nucleus.

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5

What happens to the potential energy in a hydrogenic atom as the electron moves farther from the nucleus?

As the electron moves farther from the nucleus, its potential energy becomes less negative, meaning the electron feels a weaker attraction to the nucleus.

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6

Why is reduced mass used in hydrogenic atoms?

Reduced mass is used to account for the fact that both the electron and the nucleus move. However, because the nucleus is much more massive than the electron, the reduced mass is almost the same as the mass of the electron.

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7

Why is the potential energy of the electron in a hydrogenic atom independent of angle?

The potential energy depends only on the distance between the electron and the nucleus, not the direction, which makes the problem spherically symmetric.

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8

What does the wavefunction Ψ(r,θ,ϕ) represent in the hydrogen atom?

The wavefunction describes the probability of finding an electron at a specific location, and it depends on the radial distance rrr and the angles θ and ϕ

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9

What is the significance of splitting the wavefunction into a radial and angular part?

Separating the wavefunction into radial and angular parts allows for easier solving of the Schrödinger equation, as it accounts for how the electron behaves with respect to its distance from the nucleus and its angular position.

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10

How does the kinetic energy in a hydrogenic atom change with distance and angular momentum?

The kinetic energy decreases with increasing distance from the nucleus and depends on angular momentum, where higher angular momentum results in a greater centrifugal barrier that resists the electron’s motion toward the nucleus.

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11

What does the radial wave equation describe?

The radial wave equation describes how the electron moves in a hydrogenic atom as a function of its distance from the nucleus, incorporating both kinetic and potential energy.

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12

How does angular momentum ℓ\ellℓ affect the electron’s behavior in the radial direction?

When angular momentum ℓ is zero, the electron has no angular motion, and the potential energy is solely Coulombic. When ℓ>0, the centrifugal term adds a positive contribution to the potential energy, pushing the electron away from the nucleus.

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13

What is the consequence of the centrifugal barrier at high angular momentum?

The centrifugal barrier at high angular momentum adds an effective repulsive force that prevents the electron from getting too close to the nucleus, influencing the overall shape of the wavefunction.

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14

How does the effective potential energy vary with the radial distance for different angular momenta?

For low angular momentum, the potential energy behaves similarly to a Coulombic attraction. For high angular momentum, the effective potential includes a repulsive term, meaning the electron feels both attractive and repulsive forces as it moves farther from the nucleus

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15

What happens to the electron's motion if the angular momentum is zero?

If angular momentum is zero, the electron has no rotational movement, and its motion is governed purely by the attractive force from the nucleus, without any centrifugal force to counterbalance it.

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16

What happens to the effective potential energy at large distances in a hydrogenic atom?

At large distances, the centrifugal contribution to the potential energy tends to zero more quickly than the Coulombic attraction, meaning the electron is more influenced by the Coulombic attraction at far distances.

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17

What are the two key features of the radial wavefunction near and far from the nucleus?

  • Close to the nucleus: The radial wavefunction is proportional to (r/a0)^l, meaning the electron is likely to be found close to the nucleus.

  • Far from the nucleus: The radial wavefunction approaches zero exponentially, meaning the electron has a very low probability of being found far from the nucleus.

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18

How does the radial wavefunction behave near the nucleus for higher angular momentum (l)?

For higher angular momentum, the wavefunction’s behavior near the nucleus becomes less pronounced, meaning the electron is less likely to be found near the nucleus.

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19

What role does the polynomial in r play in the radial wavefunction?

The polynomial in r describes how the radial wavefunction behaves both near and far from the nucleus, with different terms dominating depending on the region.

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20

What is the behavior of the radial wavefunction as r→0 for different values of angular momentum l?

Close to the nucleus (r→0r), the radial wavefunction behaves as r^l, meaning for larger l, the probability of finding the electron near the nucleus decreases.

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21

What happens to the dominant term of the radial wavefunction far from the nucleus?

Far from the nucleus, the dominant term in the radial wavefunction decays exponentially, meaning the likelihood of finding the electron far from the nucleus decreases rapidly.

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22

What quantum numbers define the radial and angular behavior of the electron in a hydrogenic atom?

The quantum numbers nnn (principal quantum number), lll (orbital angular momentum), and mlm_lml​ (magnetic quantum number) define the electron's behavior in a hydrogenic atom

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23

What are bound state energies in the context of hydrogenic atoms?

Bound state energies are the allowed energy levels for an electron in a hydrogenic atom, where the electron is confined to specific orbits around the nucleus, and the energy is quantized.

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24

What does it mean that the energy levels of a hydrogenic atom are n²-fold degenerate?

The n² fold degeneracy means that each energy level can accommodate multiple states with the same energy, based on different combinations of quantum numbers.

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25

What is the role of the exponential factor in the radial wavefunction?

The exponential factor in the radial wavefunction ensures that the probability of finding the electron decreases to zero as the distance from the nucleus increases.

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26

How does the factor r^l affect the radial wavefunction?

The factor r^l ensures that the wavefunction vanishes at the nucleus for non-zero angular momentum (l>0), meaning the electron has zero probability of being found exactly at the nucleus.

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27

What is the significance of the associated Laguerre polynomial in the radial wavefunction?

The associated Laguerre polynomial introduces oscillatory behavior in the wavefunction, accounting for the probability nodes (points where the probability is zero) at certain distances from the nucleus.

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28

What are the components of the total wavefunction for an electron in a hydrogenic atom?

he total wavefunction is the product of the radial wavefunction R(r)R(r)R(r) and the angular wavefunction Y(θ,ϕ), describing both the electron's radial distance and its angular position.

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29

Why can’t the radial wavefunction pass through zero at the nucleus for non-zero angular momentum?

For non-zero angular momentum (l>0), the wavefunction must vanish at the nucleus to satisfy the boundary conditions of the Schrödinger equation, meaning the electron has zero probability of being found at the nucleus.

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30

What does the principal quantum number n represent?

The principal quantum number nnn specifies the energy level of the electron, with higher values of nnn corresponding to higher energy and larger orbitals.

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31

What does the orbital angular momentum quantum number l describe?

The orbital angular momentum quantum number lll describes the shape of the electron's orbital and the magnitude of its angular momentum, with values ranging from 0 to n−1n-1n−1.

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32

What does the magnetic quantum number ml specify?

The magnetic quantum number mlm_lml​ specifies the orientation of the orbital's angular momentum along the z-axis, with possible values from −l to +l

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33

How do energy levels in hydrogenic atoms vary with the atomic number Z?

The energy levels are separated by a factor proportional to Z² meaning higher atomic numbers result in more tightly bound electrons and greater energy differences between levels.

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34

What is meant by "bound state energy" in an atom?

Bound state energy refers to the energy associated with an electron that is confined to specific orbitals within the atom, and it is negative because energy is required to remove the electron from the atom.

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35

What happens when an electron reaches unbound (positive) energy levels?

When an electron reaches unbound energy levels, it is no longer confined to the atom and becomes a free electron, meaning the atom has been ionized.

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36

Why are the energies of unbound electrons not quantized?

The energies of unbound electrons are not quantized because the electron is free and not constrained by the potential of the nucleus, allowing it to have any energy value.

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37

What is the significance of the energy equation for bound states in a hydrogenic atom?

The energy equation describes the quantized energy levels of an electron in a hydrogenic atom, where each energy level is inversely proportional to the square of the principal quantum number nnn, with lower levels more tightly bound to the nucleus.

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38

What does the Rydberg constant represent in hydrogenic atoms?

The Rydberg constant is a fundamental constant that determines the wavelengths of light emitted or absorbed by an electron transitioning between energy levels in a hydrogen atom.

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39

What is ionization energy, and what does it signify for an atom?

Ionization energy is the minimum amount of energy required to remove an electron from an atom in its ground state, indicating how tightly the electron is bound to the nucleus.

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40

What is the ionization energy of a hydrogen atom in terms of energy units?

For hydrogen, the ionization energy is approximately 13.6 eV, which corresponds to the energy needed to remove the electron from the ground state.

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41

What is the difference between a shell and a subshell in atomic orbitals?

A shell refers to all orbitals that share the same principal quantum number n, while a subshell refers to orbitals within a shell that have the same angular momentum quantum number l.

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42

How are shells labeled in atomic structure, and what do the labels represent?

Shells are labeled as K,L,M,N,… representing the principal quantum numbers n=1,2,3,4,…, which describe the electron's energy level and distance from the nucleus.

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43

How are subshells labeled in atomic structure?

Subshells are labeled by their angular momentum quantum number lll, using letters s,p,d,f,g,h,i, corresponding to l=0,1,2,3,4,5,6

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44

Why is ionization energy important in understanding atomic behavior?

Ionization energy reflects how strongly an atom holds onto its electrons, which influences the atom’s reactivity and its ability to form bonds with other atoms.

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45

How many orbitals are in a shell of a given principal quantum number n?

There are n² orbitals in a shell of principal quantum number nnn, meaning each energy level in a hydrogenic atom is n² fold degenerate.

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46

What is unique about the shape and symmetry of the sss-orbital wavefunction?

The s-orbital wavefunction is spherically symmetric, meaning it has the same value at all points equidistant from the nucleus, with no angular dependence

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47

What is the probability density of the electron near the nucleus in an s-orbital?

In an s-orbital, the probability density of the electron is highest at the nucleus, where the radial wavefunction reaches its maximum

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48

How does the compactness of an orbital affect the electron’s potential energy?

The more compact the orbital, the shorter the average distance between the electron and the nucleus, resulting in lower average potential energy due to stronger attraction to the nucleus.

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49

How does the compactness of an orbital affect the electron’s kinetic energy?

The more compact the orbital, the greater the curvature of the wavefunction, which leads to higher kinetic energy for the electron.

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50

What is the relationship between potential energy, kinetic energy, and overall energy for compact and less compact orbitals?

More compact orbitals have lower potential energy, higher kinetic energy, and typically higher overall energy compared to less compact orbitals, which have higher potential energy and lower kinetic energy.

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51

What is a boundary surface in the context of an orbital, and what does it represent?

A boundary surface is a surface that encloses a high proportion (around 90%) of the electron probability, visually representing the shape of the orbital where the electron is most likely to be found.

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52

What is an isosurface in the context of atomic orbitals?

An isosurface is a surface of constant probability density that encloses a large proportion of the electron’s probability, visually representing the characteristic shape of the orbital.

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53

What is common to all s-orbitals in terms of symmetry?

All s-orbitals are spherically symmetric, meaning the probability distribution is the same in all directions from the nucleus, though they differ in the number of radial nodes.

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54

What is a radial distribution function, and why is it important?

The radial distribution function describes the probability of finding the electron at a certain distance from the nucleus, accounting for the volume of space at that distance, and is crucial for understanding how the electron’s likelihood varies with distance from the nucleus.

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55

What does the radial distribution function for a 1s1s1s-orbital look like?

The radial distribution function for a 1s1s1s-orbital shows a peak near the nucleus and then rapidly decreases as the distance from the nucleus increases, meaning the electron is most likely to be found near the nucleus.

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56

What is a nodal plane, and what happens to the wavefunction across it?

A nodal plane is a region where the wavefunction changes sign, meaning the probability of finding the electron is zero along the plane. The wavefunction shifts from positive to negative as it crosses the nodal plane.

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57

What is the general form of the radial distribution function for an electron?

The general radial distribution function is P(r)=r²R(r)², where r² accounts for the increasing volume at greater distances, and R(r) is the radial wavefunction.

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58

What does the magnetic quantum number (ml​) specify in an atomic orbital?

The magnetic quantum number specifies the z-component of the orbital angular momentum of an electron.

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59

How does the centrifugal force affect an electron with non-zero angular momentum in a hydrogenic atom?

The centrifugal force creates an effective repulsive force that pushes the electron farther from the nucleus when its angular momentum is non-zero (l≠0).

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60

What happens to the effective potential energy for an electron in a hydrogenic atom when l=0?

When l=0, the effective potential energy is purely Coulombic and attractive, proportional to 1/r, where r is the distance from the nucleus.

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61

What is the behavior of radial wavefunctions for different l-values near the nucleus?

Radial wavefunctions for orbitals with l>0 are zero at the nucleus, while orbitals with l=0 have a finite, non-zero value at the nucleus.

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62

How does the number of radial nodes change with the principal quantum number and angular momentum quantum number?

The number of radial nodes in a wavefunction is given by n−l, where n is the principal quantum number, and l is the orbital angular momentum quantum number.

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63

What is the radial distribution function (P(r)), and why is it important?

The radial distribution function gives the probability density of finding an electron at a certain distance from the nucleus, crucial for understanding electron distribution within an atom.

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64

What does the most probable radius of an electron in a hydrogenic atom represent?

The most probable radius is the distance from the nucleus where the electron is most likely to be found, corresponding to the maximum of the radial distribution function.

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65

How does the radial distribution function behave as the principal quantum number nnn increases?

As n increases, the size of the orbital increases, and the most probable radius at which the electron is found shifts farther from the nucleus

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66

How do the shapes of p-orbitals differ from s-orbitals?

p-orbitals have an angular node and are not spherically symmetric like s-orbitals. Instead, p-orbitals have a dumbbell shape with two lobes and a nodal plane passing through the nucleus.

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