{"id":415,"date":"2022-06-23T13:13:35","date_gmt":"2022-06-23T17:13:35","guid":{"rendered":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/chapter\/6-3-development-of-quantum-theory-chemistry-2e\/"},"modified":"2022-07-04T13:23:31","modified_gmt":"2022-07-04T17:23:31","slug":"6-3-development-of-quantum-theory-chemistry-2e","status":"publish","type":"chapter","link":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/chapter\/6-3-development-of-quantum-theory-chemistry-2e\/","title":{"raw":"6.3 Development of Quantum Theory","rendered":"6.3 Development of Quantum Theory"},"content":{"raw":"<div>\r\n\r\n&nbsp;\r\n\r\n<strong><span style=\"font-family: 'Cormorant Garamond', serif;font-size: 1.602em;background-color: #cbd4b6;color: #000000\">Learning Objectives<\/span><\/strong>\r\n<div class=\"textbox textbox--learning-objectives\">\r\n\r\nBy the end of this section, you will be able to:\r\n<ul>\r\n \t<li>Extend the concept of wave\u2013particle duality that was observed in electromagnetic radiation to matter as well<\/li>\r\n \t<li>Understand the general idea of the quantum mechanical description of electrons in an atom, and that it uses the notion of three-dimensional wave functions, or orbitals, that define the distribution of probability to find an electron in a particular part of space<\/li>\r\n<\/ul>\r\n<\/div>\r\n<p id=\"fs-idm176608480\">Bohr\u2019s model explained the experimental data for the hydrogen atom and was widely accepted, but it also raised many questions. Why did electrons orbit at only fixed distances defined by a single quantum number <em>n<\/em> = 1, 2, 3, and so on, but never in between? Why did the model work so well describing hydrogen and one-electron ions, but could not correctly predict the emission spectrum for helium or any larger atoms? To answer these questions, scientists needed to completely revise the way they thought about matter.<\/p>\r\n\r\n<div id=\"fs-idm145314080\" class=\"bc-section section\">\r\n<h3><strong>Behavior in the Microscopic World<\/strong><\/h3>\r\n<p id=\"fs-idm12558432\">We know how matter behaves in the macroscopic world\u2014objects that are large enough to be seen by the naked eye follow the rules of classical physics. A billiard ball moving on a table will behave like a particle: It will continue in a straight line unless it collides with another ball or the table cushion, or is acted on by some other force (such as friction). The ball has a well-defined position and velocity (or a well-defined momentum, <em>p<\/em> = <em>mv,<\/em> defined by mass <em>m<\/em> and velocity <em>v<\/em>) at any given moment. In other words, the ball is moving in a classical trajectory. This is the typical behavior of a classical object.<\/p>\r\n<p id=\"fs-idm159209888\">When waves interact with each other, they show interference patterns that are not displayed by macroscopic particles such as the billiard ball. For example, interacting waves on the surface of water can produce interference patters similar to those shown on <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_waterw\">(Figure)<\/a>. This is a case of wave behavior on the macroscopic scale, and it is clear that particles and waves are very different phenomena in the macroscopic realm.<\/p>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_waterw\" class=\"scaled-down\">\r\n<div class=\"bc-figcaption figcaption\">An interference pattern on the water surface is formed by interacting waves. The waves are caused by reflection of water from the rocks. (credit: modification of work by Sukanto Debnath)<\/div>\r\n<span id=\"fs-idm91841872\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_waterw-1.jpg\" alt=\"A photograph is shown of ripples in water. The ripples display an interference pattern with each other.\" \/><\/span>\r\n\r\n<\/div>\r\n<p id=\"fs-idm161134656\">As technological improvements allowed scientists to probe the microscopic world in greater detail, it became increasingly clear by the 1920s that very small pieces of matter follow a different set of rules from those we observe for large objects. The unquestionable separation of waves and particles was no longer the case for the microscopic world.<\/p>\r\n<p id=\"fs-idm151523216\">One of the first people to pay attention to the special behavior of the microscopic world was Louis <span class=\"no-emphasis\">de Broglie<\/span>. He asked the question: If electromagnetic radiation can have particle-like character, can electrons and other submicroscopic particles exhibit wavelike character? In his 1925 doctoral dissertation, de Broglie extended the wave\u2013particle duality of light to material particles. He predicted that a particle with mass <em>m<\/em> and velocity <em>v<\/em> (that is, with linear momentum <em>p<\/em>) should also exhibit the behavior of a wave with a wavelength value <em>\u03bb<\/em>, given by this expression in which <em>h<\/em> is the familiar Planck\u2019s constant:<\/p>\r\n\r\n<div id=\"fs-idp110855072\"><img class=\"wp-image-1388 aligncenter\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/6.3a.png\" alt=\"\" width=\"119\" height=\"45\" \/><\/div>\r\n<p id=\"fs-idm234395904\">This is called the <em>de Broglie wavelength<\/em>. Unlike the other values of <em>\u03bb<\/em> discussed in this chapter, the de Broglie wavelength is a characteristic of particles and other bodies, not electromagnetic radiation (note that this equation involves velocity [<em>v<\/em>, m\/s], not frequency [<em>\u03bd<\/em>, Hz]. Although these two symbols appear nearly identical, they mean very different things). Where Bohr had postulated the electron as being a particle orbiting the nucleus in quantized orbits, de Broglie argued that Bohr\u2019s assumption of quantization can be explained if the electron is considered not as a particle, but rather as a circular standing wave such that only an integer number of wavelengths could fit exactly within the orbit (<a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_elecw\">(Figure)<\/a>).<\/p>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_elecw\" class=\"scaled-down\">\r\n<div class=\"bc-figcaption figcaption\">If an electron is viewed as a wave circling around the nucleus, an integer number of wavelengths must fit into the orbit for this standing wave behavior to be possible.<\/div>\r\n<span id=\"fs-idm68754864\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_elecw-1.jpg\" alt=\"This figure includes a circle formed from a dashed line. A sinusoidal wave pattern indicated with a solid red line is wrapped around the circle, centered about the edge of the circle. Line segments extend outward from the circle extending through 2 wave crests along the circle. A double ended arrow is drawn between these segments and is labeled, \u201cwavelength, lambda.\u201d A dashed double headed arrow is drawn from the center to the edge of the circle and is labeled, \u201cradius r.\u201d\" \/><\/span>\r\n\r\n<\/div>\r\n<p id=\"fs-idp34135808\">For a circular orbit of radius <em>r<\/em>, the circumference is 2<em>\u03c0r<\/em>, and so de Broglie\u2019s condition is:<\/p>\r\n\r\n<div id=\"fs-idm78157712\" style=\"text-align: center\">2\u03c0<em>r<\/em> = <em>n<\/em>\u03bb , <em>n <\/em>= 1, 2, 3, \u2026<\/div>\r\n<p id=\"fs-idm114335872\">Shortly after de Broglie proposed the wave nature of matter, two scientists at Bell Laboratories, C. J. <span class=\"no-emphasis\">Davisson<\/span> and L. H. <span class=\"no-emphasis\">Germer<\/span>, demonstrated experimentally that electrons can exhibit wavelike behavior by showing an interference pattern for electrons travelling through a regular atomic pattern in a crystal. The regularly spaced atomic layers served as slits, as used in other interference experiments. Since the spacing between the layers serving as slits needs to be similar in size to the wavelength of the tested wave for an interference pattern to form, Davisson and Germer used a crystalline nickel target for their \u201cslits,\u201d since the spacing of the atoms within the lattice was approximately the same as the de Broglie wavelengths of the electrons that they used. <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_Electrnin\">(Figure)<\/a> shows an interference pattern. It is strikingly similar to the interference patterns for light shown in Section 6.1 for light passing through two closely spaced, narrow slits. The wave\u2013particle duality of matter can be seen in <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_Electrnin\">(Figure)<\/a> by observing what happens if electron collisions are recorded over a long period of time. Initially, when only a few electrons have been recorded, they show clear particle-like behavior, having arrived in small localized packets that appear to be random. As more and more electrons arrived and were recorded, a clear interference pattern that is the hallmark of wavelike behavior emerged. Thus, it appears that while electrons are small localized particles, their motion does not follow the equations of motion implied by classical mechanics, but instead it is governed by some type of a wave equation. Thus the wave\u2013particle duality first observed with photons is actually a fundamental behavior intrinsic to all quantum particles.<\/p>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_Electrnin\" class=\"bc-figure figure\">\r\n<div class=\"bc-figcaption figcaption\">(a) The interference pattern for electrons passing through very closely spaced slits demonstrates that quantum particles such as electrons can exhibit wavelike behavior. (b) The experimental results illustrated here demonstrate the wave\u2013particle duality in electrons.<\/div>\r\n<span id=\"fs-idm29319408\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_Electrnin-1.jpg\" alt=\"This figure has two parts. Part a shows a diagram of an electron source emitting waves that pass through two narrow slits in a barrier. A wave interference pattern results on the opposite side of the barrier that result in evenly spaced, relatively wide horizontal grey lines on a black surface. The black surface is placed at a distance beyond the barrier. Part b shows an electron source at the far left. Two gold arrows point toward two narrow horizontal slits in a barrier. Around these arrows are many small golden dots. On the right side of the barrier, the gold dots are more widely dispersed. A black surface a distance beyond the barrier shows evenly, yet widely dispersed gold dots. An arrow is present below this black surface and is labeled, \u201cTime.\u201d A second black surface is shown to the right that has many more golden dots that appear to be organizing into a pattern of evenly spaced horizontal line segments. A third black surface is shown even further to the right in which many more gold dots are shown in a very clearly established, evenly spaced pattern of horizontal line segments.\" \/><\/span>\r\n\r\n<\/div>\r\n<div id=\"fs-idm22236656\" class=\"chemistry link-to-learning\">\r\n\r\n&nbsp;\r\n<p id=\"fs-idp43121536\">View the Dr. Quantum \u2013 Double Slit Experiment <a href=\"http:\/\/openstaxcollege.org\/l\/16duality\">cartoon<\/a> for an easy-to-understand description of wave\u2013particle duality and the associated experiments.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"fs-idm2526400\" class=\"bc-section section\">\r\n<h3><strong>The Quantum\u2013Mechanical Model of an Atom<\/strong><\/h3>\r\n<p id=\"fs-idm146032560\">Shortly after de Broglie published his ideas that the electron in a hydrogen atom could be better thought of as being a circular standing wave instead of a particle moving in quantized circular orbits, Erwin Schr\u00f6dinger extended de Broglie\u2019s work by deriving what is today known as the Schr\u00f6dinger equation. When Schr\u00f6dinger applied his equation to hydrogen-like atoms, he was able to reproduce Bohr\u2019s expression for the energy and, thus, the Rydberg formula governing hydrogen spectra. Schr\u00f6dinger described electrons as three-dimensional stationary waves, or wavefunctions, represented by the Greek letter psi, <em>\u03c8<\/em>. A few years later, Max <span class=\"no-emphasis\">Born<\/span> proposed an interpretation of the wavefunction <em>\u03c8<\/em> that is still accepted today: Electrons are still particles, and so the waves represented by <em>\u03c8<\/em> are not physical waves but, instead, are complex probability amplitudes. The square of the magnitude of a wavefunction, <em>\u03c8<sup>2<\/sup>,<\/em>\u00a0describes the probability of the quantum particle being present near a certain location in space. This means that wavefunctions can be used to determine the distribution of the electron\u2019s density with respect to the nucleus in an atom. In the most general form, the Schr\u00f6dinger equation can be written as:<\/p>\r\n\r\n<div id=\"fs-idm195751440\"><img class=\"wp-image-1390 aligncenter\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/6.3b.png\" alt=\"\" width=\"94\" height=\"35\" \/><\/div>\r\n<p id=\"fs-idm1012848\"><img class=\"alignnone wp-image-1391\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/6.3c.png\" alt=\"\" width=\"24\" height=\"24\" \/> is the Hamiltonian operator, a set of mathematical operations representing the total energy of the quantum particle (such as an electron in an atom), <em>\u03c8<\/em> is the wavefunction of this particle that can be used to find the special distribution of the probability of finding the particle, and <em>E<\/em> is the actual value of the total energy of the particle.<\/p>\r\n<p id=\"fs-idm134389936\">Schr\u00f6dinger\u2019s work, as well as that of many other scientists following in their footsteps, is generally referred to as quantum mechanics.<\/p>\r\n\r\n<div id=\"fs-idm148452752\" class=\"chemistry link-to-learning\">\r\n<p id=\"fs-idp90020512\">You may also have heard of Schr\u00f6dinger because of his famous thought experiment. <a href=\"http:\/\/openstaxcollege.org\/l\/16superpos\">This story<\/a> explains the concepts of superposition and entanglement as related to a cat in a box with poison.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"fs-idp27284864\" class=\"bc-section section\">\r\n<h3><strong>Understanding Quantum Theory of Electrons in Atoms<\/strong><\/h3>\r\nIn our current quantum mechanical model of the atom, we can no longer accept that electrons travel in set orbits around the nucleus.\u00a0 However, we must still accept the idea of quantized energy levels, as they arose from experimental observations of actual line spectra.\r\n\r\nNow, we interpret the energy levels as corresponding to orbitals in the atom.\u00a0 An <strong>atomic orbital<\/strong> is interpreted as a general region in an atom within which an electron is most probable to reside.\u00a0 \u00a0But in truth, they are the wavefunctions that are solutions to the Schrodinger equation.\u00a0 These orbital wavefunctions describe the <strong>probability<\/strong> of finding an electron (<em>\u03c8<sup>2<\/sup><\/em>, as described above).\r\n<p id=\"fs-idm171695728\">As before, the energy levels are labeled with an <em>n<\/em> value, where <em>n<\/em> = 1, 2, 3, \u2026. This number, <strong>n<\/strong>, is referred to as the <strong>principal quantum number<\/strong>. Generally speaking, the energy of an electron in an atom is greater for greater values of <em>n<\/em>. The principal quantum number is\u00a0 also related to the average distance the electron is from the nucleus. The positively charged protons in the nucleus stabilize the electronic orbitals by electrostatic attraction between the positive charges of the protons and the negative charges of the electrons. So the further away the electron is from the nucleus, the greater the energy it has.<\/p>\r\n<p id=\"fs-idm166868080\">This quantum mechanical model for where electrons reside in an atom can be used to look at electronic transitions, the events when an electron moves from one energy level to another. If the transition is to a higher energy level, energy is absorbed, and the energy change has a positive value. To obtain the amount of energy necessary for the transition to a higher energy level, a photon is absorbed by the atom. A transition to a lower energy level involves a release of energy, and the energy change is negative. This process is accompanied by emission of a photon by the atom.<\/p>\r\n<p id=\"fs-idm184616288\">There are certain distances from the nucleus at which the probability density of finding an electron located at a particular orbital is zero. In other words, the value of the wavefunction <em>\u03c8<\/em> is zero at this distance for this orbital. Such a value of radius <em>r<\/em> is called a <strong>node<\/strong>.<\/p>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_sOrbit\" class=\"bc-figure figure\">\r\n<div class=\"bc-figcaption figcaption\">The graphs show the probability (<em>y<\/em> axis) of finding an electron for the 1<em>s<\/em>, 2<em>s<\/em>, 3<em>s<\/em> orbitals as a function of distance from the nucleus.<\/div>\r\n<span id=\"fs-idm165672208\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_sorbit-1.jpg\" alt=\"This figure provides images and graphs to illustrate the probability of finding an electron in 1 s, 2 s, and 3 s orbitals as a function of the distance from the nucleus. The 1 s orbital is shown as a sphere with a chunk missing. Below it, a graph is marked on its horizontal axis at 0 and 50 p m. The related curve quickly reaches a maximum height and rapidly declines. The label, \u201c1 s\u201d appears below the graph. The 2 s orbital is shown as a red sphere with a blue middle. A chunk is missing from the sphere. A graph below it is marked on its horizontal axis at 0, 50, and 100 p m. The related curve quickly reaches a relative maximum height, a significantly higher absolute maximum height, and then rapidly declines. The label \u201c2s\u201d appears below it. The 3 s orbital is a blue sphere with a red sphere and another blue sphere at its core. A graph below it is marked on its horizontal axis at 0, 50, 100, and 150 p m. The related curve quickly reaches a relative maximum height, a second relative maximum height, a significantly higher absolute maximum, and then declines more gradually than illustrated in the previous 2 graphs. The label, \u201c3 s,\u201d appears below the graph.\" \/><\/span>\r\n\r\n<\/div>\r\n<p id=\"fs-idm158802176\">The electron density distribution of an <em>s <\/em>orbital is spherical and a <em>p<\/em> orbital has a dumbbell shape. The <em>d<\/em> and <em>f<\/em> orbitals are more complex. These shapes represent the three-dimensional regions within which the electron is likely to be found.<\/p>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_Oshapes\" class=\"bc-figure figure\">\r\n<div class=\"bc-figcaption figcaption\">Shapes of <em>s<\/em>, <em>p<\/em>, <em>d<\/em>, and <em>f<\/em> orbitals.<\/div>\r\n<span id=\"fs-idm313200\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_Oshapes-1.jpg\" alt=\"This diagram illustrates the shapes and quantities of all s, p, d, and f orbitals. The s sublevel is composed of a single spherical orbital. The p sublevel is composed of 3 dumbbell shaped orbitals oriented along the x, y, and z axes. The five d sublevels and seven f sublevels are considerably more complex.\" \/><\/span>\r\n\r\n<\/div>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_subshells\" class=\"bc-figure figure\">\r\n<div><\/div>\r\n<div class=\"bc-figcaption figcaption\">The chart shows the energies of electron orbitals in a multi-electron atom.<\/div>\r\n<span id=\"fs-idm149251120\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_subshells-1.jpg\" alt=\"This diagram shown has an upward pointing arrow at the left which is labeled \u201cE.\u201d To the right of this arrow near the bottom of the image is a single line which is labeled, \u201c1 s.\u201d Above and just to the right is another black line that is labeled, \u201c2 s.\u201d Slightly up and to the right is a grouping of three black lines labeled, \u201c2 p.\u201d Above and to the right is a single black line labeled, \u201c3 s.\u201d Slightly up and to the right is a grouping of three black lines that are labeled, \u201c3 p.\u201d Just above and to the right is a grouping of 5 black lines labeled, \u201c3 d.\u201d Slightly below and to the right is a single black line which is labeled, \u201c4 s.\u201d Just above and to the right, at a level slightly higher than the previous black lines, is a grouping of three black lines all labeled, \u201c4 p.\u201d\" \/><\/span>\r\n\r\n<\/div>\r\n<p id=\"fs-idm83747248\"><a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_subshells\">(Figure)<\/a> illustrates the energy levels for various orbitals. The number before the orbital name (such as 2<em>s<\/em>, 3<em>p<\/em>, and so forth) stands for the principal quantum number, <em>n<\/em>. The letter in the orbital name defines the sublevel: <em>s<\/em> orbitals, <em>p<\/em> orbitals, <em>d<\/em> orbitals, etc. \u00a0In the case of a hydrogen atom or a one-electron ion (such as He<sup>+<\/sup>, Li<sup>2+<\/sup>, and so on), energies of all the orbitals with the same <em>n<\/em> are the same. This is called a degeneracy, and the energy levels for the same principal quantum number, <em>n<\/em>, are called <strong>degenerate<\/strong> orbitals. However, in atoms with more than one electron, this degeneracy is eliminated by the electron\u2013electron interactions, and orbitals that belong to different sublevels have different energies, as shown on <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_subshells\">(Figure)<\/a>. Orbitals within the same sublevel are still degenerate and have the same energy.<\/p>\r\n<p id=\"fs-idm136117120\">So far, we have been considering the orbitals, which we interpret is the regions in space where electrons can be found.\u00a0 Now we will consider the behavior of the electrons themselves. \u00a0 In an atom, each electron acts as a tiny magnet or a tiny rotating object with an angular momentum; we describe this intrinsic electron \u201crotation\u201d in terms of a property called electron spin.<\/p>\r\n<p id=\"fs-idm82083456\">An electron can only \u201cspin\u201d in one of two quantized states. One is termed the \u03b1 state (\"spin up\"). \u00a0The other is called the \u03b2 state (\"spin down\"). Any electron, regardless of the atomic orbital it is located in, can only be spin up or spin down.<\/p>\r\n&nbsp;\r\n<div id=\"CNX_Chem_06_03_spin\" class=\"scaled-down\">\r\n<div class=\"bc-figcaption figcaption\">Electrons in an external magnetic field.<\/div>\r\n<span id=\"fs-idm7831072\"><img src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_spin-1.jpg\" alt=\"This diagram has an upward pointing arrow at the left which is labeled, \u201cB subscript 0.\u201d To the right, two spheres are shown. The first has a gray square at the top labeled, \u201cN,\u201d and a second gray square at the bottom labeled, \u201cS.\u201d A curved arrow is pointing right across the surface of the sphere and a gray arrow points upward through the center of the sphere. This sphere is labeled, \u201cSpin plus one-half, spin-up.\u201d The sphere just to the right has a gray square above it labeled, \u201cS,\u201d and a gray square below it labeled, \u201cN.\u201d This sphere has a curved arrow on its surface that is directed to the left and a gray arrow through the center of the sphere that points downward. This sphere is labeled, \u201cSpin negative one-half spin-down.\u201d\" \/><\/span>\r\n\r\n<\/div>\r\n<p id=\"fs-idm91739088\"><a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_spin\">(Figure)<\/a> illustrates this phenomenon. An electron acts like a tiny magnet. Its moment is directed up (in the positive direction of the <em>z<\/em> axis) and down (in the negative <em>z<\/em> direction). A magnet has a lower energy if its magnetic moment is aligned with the external magnetic field (the left electron on <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_spin\">(Figure)<\/a>) and a higher energy for the magnetic moment being opposite to the applied field. This is true even for an electron occupying the same orbital in an atom.<\/p>\r\n\r\n<\/div>\r\n<div id=\"fs-idm162650560\" class=\"bc-section section\">\r\n<h3><strong>The Pauli Exclusion Principle<\/strong><\/h3>\r\n<p id=\"fs-idm225354640\">Now that we have looked at the orbitals and the electrons separately, we are ready to consider how electrons are placed in orbitals within an atom.\u00a0 \u00a0The <strong>Pauli exclusion principle, <\/strong>named for an Austrian physicist Wolfgang Pauli, can be formulated as follows: no two electrons in the same orbital can have the same spin.\u00a0 Since there are only two spin states, any atomic orbital can be populated by only zero, one, or two electrons.<\/p>\r\n\r\n<div id=\"fs-idm169030688\" class=\"textbox textbox--examples\">\r\n<p id=\"fs-idm68824256\"><strong>Maximum Number of Electrons:<\/strong><\/p>\r\nCalculate the maximum number of electrons that can occupy an energy level with (a) <em>n<\/em> = 2, (b) <em>n<\/em> = 5, and (c) <em>n<\/em> as a variable. Note you are only looking at the orbitals with the specified <em>n<\/em> value, not those at lower energies.\r\n<p id=\"fs-idm174701168\"><strong>Solution:<\/strong><\/p>\r\n(a) When <em>n<\/em> = 2, there are four orbitals (a single 2<em>s<\/em> orbital, and three orbitals labeled 2<em>p<\/em>). These four orbitals can contain eight electrons.\r\n<p id=\"fs-idm146693328\">(b) When <em>n<\/em> = 5, there are five sublevels of orbitals that we need to sum:<\/p>\r\n\r\n<div id=\"fs-idm204408304\" style=\"text-align: center\">1 orbital labelled 5<em>s<\/em><\/div>\r\n<div style=\"text-align: center\">3 orbitals labelled 5<em>p<\/em><\/div>\r\n<div style=\"text-align: center\">5 orbitals labelled 5<em>d<\/em><\/div>\r\n<div style=\"text-align: center\">7 orbitals labelled 5<em>f<\/em><\/div>\r\n<div style=\"text-align: center\"><span style=\"text-decoration: underline\">9 orbitals labelled 5<em>g<\/em><\/span><\/div>\r\n<div style=\"text-align: center\">25 orbitals total<\/div>\r\n<div><\/div>\r\n<p id=\"fs-idm145553968\">Again, each orbital holds two electrons, so 50 electrons can fit in this energy level.<\/p>\r\n<p id=\"fs-idm106652512\">(c) The number of orbitals in any energy level <em>n<\/em> will equal <em>n<\/em><sup>2<\/sup><sub>.<\/sub> There can be up to two electrons in each orbital, so the maximum number of electrons will be 2<em>n<\/em><sup>2<\/sup>.<\/p>\r\n<p id=\"fs-idm13201440\"><strong>Check Your Learning:<\/strong><\/p>\r\nIf an energy level contains a maximum of 32 electrons, what is the principal quantum number, <em>n<\/em>?\r\n\r\n&nbsp;\r\n<div id=\"fs-idm166820736\">\r\n<div><strong>Answer:<\/strong><\/div>\r\n<p id=\"fs-idm135023952\"><em>n<\/em> = 4<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"fs-idm55472464\" class=\"summary\">\r\n<h3><strong>Key Concepts and Summary<\/strong><\/h3>\r\n<p id=\"fs-idm175984864\">Macroscopic objects act as particles. Microscopic objects (such as electrons) have properties of both a particle and a wave. Their exact trajectories cannot be determined. The quantum mechanical model of atoms describes the three-dimensional position of the electron in a <em>probabilistic<\/em> manner according to a mathematical function called a wavefunction, often denoted as <em>\u03c8<\/em>. Atomic wavefunctions are also called orbitals. The squared magnitude of the wavefunction describes the distribution of the probability of finding the electron in a particular region in space. Therefore, atomic orbitals describe where electrons in an atom are most likely to be found.<\/p>\r\n\r\n<\/div>\r\n<div id=\"fs-idm162744496\" class=\"exercises\">\r\n<div id=\"fs-idm24126560\">\r\n<div id=\"fs-idm29306320\"><\/div>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox shaded\">\r\n<h3><strong>Glossary<\/strong><\/h3>\r\n<dl id=\"fs-idm176142304\">\r\n \t<dt>secondary (angular momentum) quantum number (<em>l<\/em>)<\/dt>\r\n \t<dd id=\"fs-idm128619824\">quantum number distinguishing the different shapes of orbitals; it is also a measure of the orbital angular momentum<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm147438368\">\r\n \t<dt>atomic orbital<\/dt>\r\n \t<dd id=\"fs-idm109054128\">mathematical function that describes the behavior of an electron in an atom (also called the wavefunction)<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idp12032\">\r\n \t<dt><em>d<\/em> orbital<\/dt>\r\n \t<dd id=\"fs-idm164271760\">region of space with high electron density that is either four lobed or contains a dumbbell and torus shape; describes orbitals with <em>l<\/em> = 2.<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm442273488\">\r\n \t<dt>degenerate orbitals<\/dt>\r\n \t<dd id=\"fs-idm476031024\">orbitals that have the same energy<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm56391008\">\r\n \t<dt>electron density<\/dt>\r\n \t<dd id=\"fs-idp58829584\">a measure of the probability of locating an electron in a particular region of space, it is equal to the squared absolute value of the wave function <em>\u03c8<\/em><\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm174396336\">\r\n \t<dt>energy level<\/dt>\r\n \t<dd id=\"fs-idm12350992\">atomic orbitals with the same principal quantum number, <em>n<\/em><\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm166903488\">\r\n \t<dt>magnetic quantum number (<em>m<sub>l<\/sub><\/em>)<\/dt>\r\n \t<dd id=\"fs-idm147105616\">quantum number signifying the orientation of an atomic orbital around the nucleus<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm147658080\">\r\n \t<dt><em>p<\/em> orbital<\/dt>\r\n \t<dd id=\"fs-idm165030336\">dumbbell-shaped region of space with high electron density, describes orbitals with <em>l<\/em> = 1<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm120400016\">\r\n \t<dt>Pauli exclusion principle<\/dt>\r\n \t<dd id=\"fs-idp43763072\">specifies that no two electrons in an atom can have the same value for all four quantum numbers<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm140352128\">\r\n \t<dt>principal quantum number (<em>n<\/em>)<\/dt>\r\n \t<dd id=\"fs-idm13159072\">quantum number specifying the energy level an electron occupies in an atom<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm160875424\">\r\n \t<dt>quantum mechanics<\/dt>\r\n \t<dd id=\"fs-idm48323504\">field of study that includes quantization of energy and wave-particle duality to describe matter<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm144189680\">\r\n \t<dt><em>s<\/em> orbital<\/dt>\r\n \t<dd id=\"fs-idm168786512\">spherical region of space with high electron density, describes orbitals with <em>l<\/em> = 0<\/dd>\r\n<\/dl>\r\n<dl>\r\n \t<dd><\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm137493808\">\r\n \t<dt>spin quantum number (<em>m<sub>s<\/sub><\/em>)<\/dt>\r\n \t<dd id=\"fs-idm165810304\">number specifying the electron spin direction, either \u00bd or -\u00bd<\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm148470816\">\r\n \t<dt>sublevel<\/dt>\r\n \t<dd id=\"fs-idm136103056\">atomic orbitals with the same values of <em>n<\/em> and <em>l<\/em><\/dd>\r\n<\/dl>\r\n<dl id=\"fs-idm163956768\">\r\n \t<dt>wavefunction (<em>\u03c8<\/em>)<\/dt>\r\n \t<dd id=\"fs-idm106660816\">mathematical description of an atomic orbital that describes the shape of the orbital; it can be used to calculate the probability of finding the electron at any given location in the orbital, as well as dynamical variables such as the energy and the angular momentum<\/dd>\r\n<\/dl>\r\n<\/div>\r\n&lt;!-- pb_fixme --&gt;\r\n\r\n<\/div>\r\n<div>&lt;!-- pb_fixme --&gt;&lt;!-- pb_fixme --&gt;<\/div>","rendered":"<div>\n<p>&nbsp;<\/p>\n<p><strong><span style=\"font-family: 'Cormorant Garamond', serif;font-size: 1.602em;background-color: #cbd4b6;color: #000000\">Learning Objectives<\/span><\/strong><\/p>\n<div class=\"textbox textbox--learning-objectives\">\n<p>By the end of this section, you will be able to:<\/p>\n<ul>\n<li>Extend the concept of wave\u2013particle duality that was observed in electromagnetic radiation to matter as well<\/li>\n<li>Understand the general idea of the quantum mechanical description of electrons in an atom, and that it uses the notion of three-dimensional wave functions, or orbitals, that define the distribution of probability to find an electron in a particular part of space<\/li>\n<\/ul>\n<\/div>\n<p id=\"fs-idm176608480\">Bohr\u2019s model explained the experimental data for the hydrogen atom and was widely accepted, but it also raised many questions. Why did electrons orbit at only fixed distances defined by a single quantum number <em>n<\/em> = 1, 2, 3, and so on, but never in between? Why did the model work so well describing hydrogen and one-electron ions, but could not correctly predict the emission spectrum for helium or any larger atoms? To answer these questions, scientists needed to completely revise the way they thought about matter.<\/p>\n<div id=\"fs-idm145314080\" class=\"bc-section section\">\n<h3><strong>Behavior in the Microscopic World<\/strong><\/h3>\n<p id=\"fs-idm12558432\">We know how matter behaves in the macroscopic world\u2014objects that are large enough to be seen by the naked eye follow the rules of classical physics. A billiard ball moving on a table will behave like a particle: It will continue in a straight line unless it collides with another ball or the table cushion, or is acted on by some other force (such as friction). The ball has a well-defined position and velocity (or a well-defined momentum, <em>p<\/em> = <em>mv,<\/em> defined by mass <em>m<\/em> and velocity <em>v<\/em>) at any given moment. In other words, the ball is moving in a classical trajectory. This is the typical behavior of a classical object.<\/p>\n<p id=\"fs-idm159209888\">When waves interact with each other, they show interference patterns that are not displayed by macroscopic particles such as the billiard ball. For example, interacting waves on the surface of water can produce interference patters similar to those shown on <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_waterw\">(Figure)<\/a>. This is a case of wave behavior on the macroscopic scale, and it is clear that particles and waves are very different phenomena in the macroscopic realm.<\/p>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_waterw\" class=\"scaled-down\">\n<div class=\"bc-figcaption figcaption\">An interference pattern on the water surface is formed by interacting waves. The waves are caused by reflection of water from the rocks. (credit: modification of work by Sukanto Debnath)<\/div>\n<p><span id=\"fs-idm91841872\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_waterw-1.jpg\" alt=\"A photograph is shown of ripples in water. The ripples display an interference pattern with each other.\" \/><\/span><\/p>\n<\/div>\n<p id=\"fs-idm161134656\">As technological improvements allowed scientists to probe the microscopic world in greater detail, it became increasingly clear by the 1920s that very small pieces of matter follow a different set of rules from those we observe for large objects. The unquestionable separation of waves and particles was no longer the case for the microscopic world.<\/p>\n<p id=\"fs-idm151523216\">One of the first people to pay attention to the special behavior of the microscopic world was Louis <span class=\"no-emphasis\">de Broglie<\/span>. He asked the question: If electromagnetic radiation can have particle-like character, can electrons and other submicroscopic particles exhibit wavelike character? In his 1925 doctoral dissertation, de Broglie extended the wave\u2013particle duality of light to material particles. He predicted that a particle with mass <em>m<\/em> and velocity <em>v<\/em> (that is, with linear momentum <em>p<\/em>) should also exhibit the behavior of a wave with a wavelength value <em>\u03bb<\/em>, given by this expression in which <em>h<\/em> is the familiar Planck\u2019s constant:<\/p>\n<div id=\"fs-idp110855072\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1388 aligncenter\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/6.3a.png\" alt=\"\" width=\"119\" height=\"45\" \/><\/div>\n<p id=\"fs-idm234395904\">This is called the <em>de Broglie wavelength<\/em>. Unlike the other values of <em>\u03bb<\/em> discussed in this chapter, the de Broglie wavelength is a characteristic of particles and other bodies, not electromagnetic radiation (note that this equation involves velocity [<em>v<\/em>, m\/s], not frequency [<em>\u03bd<\/em>, Hz]. Although these two symbols appear nearly identical, they mean very different things). Where Bohr had postulated the electron as being a particle orbiting the nucleus in quantized orbits, de Broglie argued that Bohr\u2019s assumption of quantization can be explained if the electron is considered not as a particle, but rather as a circular standing wave such that only an integer number of wavelengths could fit exactly within the orbit (<a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_elecw\">(Figure)<\/a>).<\/p>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_elecw\" class=\"scaled-down\">\n<div class=\"bc-figcaption figcaption\">If an electron is viewed as a wave circling around the nucleus, an integer number of wavelengths must fit into the orbit for this standing wave behavior to be possible.<\/div>\n<p><span id=\"fs-idm68754864\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_elecw-1.jpg\" alt=\"This figure includes a circle formed from a dashed line. A sinusoidal wave pattern indicated with a solid red line is wrapped around the circle, centered about the edge of the circle. Line segments extend outward from the circle extending through 2 wave crests along the circle. A double ended arrow is drawn between these segments and is labeled, \u201cwavelength, lambda.\u201d A dashed double headed arrow is drawn from the center to the edge of the circle and is labeled, \u201cradius r.\u201d\" \/><\/span><\/p>\n<\/div>\n<p id=\"fs-idp34135808\">For a circular orbit of radius <em>r<\/em>, the circumference is 2<em>\u03c0r<\/em>, and so de Broglie\u2019s condition is:<\/p>\n<div id=\"fs-idm78157712\" style=\"text-align: center\">2\u03c0<em>r<\/em> = <em>n<\/em>\u03bb , <em>n <\/em>= 1, 2, 3, \u2026<\/div>\n<p id=\"fs-idm114335872\">Shortly after de Broglie proposed the wave nature of matter, two scientists at Bell Laboratories, C. J. <span class=\"no-emphasis\">Davisson<\/span> and L. H. <span class=\"no-emphasis\">Germer<\/span>, demonstrated experimentally that electrons can exhibit wavelike behavior by showing an interference pattern for electrons travelling through a regular atomic pattern in a crystal. The regularly spaced atomic layers served as slits, as used in other interference experiments. Since the spacing between the layers serving as slits needs to be similar in size to the wavelength of the tested wave for an interference pattern to form, Davisson and Germer used a crystalline nickel target for their \u201cslits,\u201d since the spacing of the atoms within the lattice was approximately the same as the de Broglie wavelengths of the electrons that they used. <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_Electrnin\">(Figure)<\/a> shows an interference pattern. It is strikingly similar to the interference patterns for light shown in Section 6.1 for light passing through two closely spaced, narrow slits. The wave\u2013particle duality of matter can be seen in <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_Electrnin\">(Figure)<\/a> by observing what happens if electron collisions are recorded over a long period of time. Initially, when only a few electrons have been recorded, they show clear particle-like behavior, having arrived in small localized packets that appear to be random. As more and more electrons arrived and were recorded, a clear interference pattern that is the hallmark of wavelike behavior emerged. Thus, it appears that while electrons are small localized particles, their motion does not follow the equations of motion implied by classical mechanics, but instead it is governed by some type of a wave equation. Thus the wave\u2013particle duality first observed with photons is actually a fundamental behavior intrinsic to all quantum particles.<\/p>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_Electrnin\" class=\"bc-figure figure\">\n<div class=\"bc-figcaption figcaption\">(a) The interference pattern for electrons passing through very closely spaced slits demonstrates that quantum particles such as electrons can exhibit wavelike behavior. (b) The experimental results illustrated here demonstrate the wave\u2013particle duality in electrons.<\/div>\n<p><span id=\"fs-idm29319408\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_Electrnin-1.jpg\" alt=\"This figure has two parts. Part a shows a diagram of an electron source emitting waves that pass through two narrow slits in a barrier. A wave interference pattern results on the opposite side of the barrier that result in evenly spaced, relatively wide horizontal grey lines on a black surface. The black surface is placed at a distance beyond the barrier. Part b shows an electron source at the far left. Two gold arrows point toward two narrow horizontal slits in a barrier. Around these arrows are many small golden dots. On the right side of the barrier, the gold dots are more widely dispersed. A black surface a distance beyond the barrier shows evenly, yet widely dispersed gold dots. An arrow is present below this black surface and is labeled, \u201cTime.\u201d A second black surface is shown to the right that has many more golden dots that appear to be organizing into a pattern of evenly spaced horizontal line segments. A third black surface is shown even further to the right in which many more gold dots are shown in a very clearly established, evenly spaced pattern of horizontal line segments.\" \/><\/span><\/p>\n<\/div>\n<div id=\"fs-idm22236656\" class=\"chemistry link-to-learning\">\n<p>&nbsp;<\/p>\n<p id=\"fs-idp43121536\">View the Dr. Quantum \u2013 Double Slit Experiment <a href=\"http:\/\/openstaxcollege.org\/l\/16duality\">cartoon<\/a> for an easy-to-understand description of wave\u2013particle duality and the associated experiments.<\/p>\n<\/div>\n<\/div>\n<div id=\"fs-idm2526400\" class=\"bc-section section\">\n<h3><strong>The Quantum\u2013Mechanical Model of an Atom<\/strong><\/h3>\n<p id=\"fs-idm146032560\">Shortly after de Broglie published his ideas that the electron in a hydrogen atom could be better thought of as being a circular standing wave instead of a particle moving in quantized circular orbits, Erwin Schr\u00f6dinger extended de Broglie\u2019s work by deriving what is today known as the Schr\u00f6dinger equation. When Schr\u00f6dinger applied his equation to hydrogen-like atoms, he was able to reproduce Bohr\u2019s expression for the energy and, thus, the Rydberg formula governing hydrogen spectra. Schr\u00f6dinger described electrons as three-dimensional stationary waves, or wavefunctions, represented by the Greek letter psi, <em>\u03c8<\/em>. A few years later, Max <span class=\"no-emphasis\">Born<\/span> proposed an interpretation of the wavefunction <em>\u03c8<\/em> that is still accepted today: Electrons are still particles, and so the waves represented by <em>\u03c8<\/em> are not physical waves but, instead, are complex probability amplitudes. The square of the magnitude of a wavefunction, <em>\u03c8<sup>2<\/sup>,<\/em>\u00a0describes the probability of the quantum particle being present near a certain location in space. This means that wavefunctions can be used to determine the distribution of the electron\u2019s density with respect to the nucleus in an atom. In the most general form, the Schr\u00f6dinger equation can be written as:<\/p>\n<div id=\"fs-idm195751440\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1390 aligncenter\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/6.3b.png\" alt=\"\" width=\"94\" height=\"35\" \/><\/div>\n<p id=\"fs-idm1012848\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1391\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/6.3c.png\" alt=\"\" width=\"24\" height=\"24\" \/> is the Hamiltonian operator, a set of mathematical operations representing the total energy of the quantum particle (such as an electron in an atom), <em>\u03c8<\/em> is the wavefunction of this particle that can be used to find the special distribution of the probability of finding the particle, and <em>E<\/em> is the actual value of the total energy of the particle.<\/p>\n<p id=\"fs-idm134389936\">Schr\u00f6dinger\u2019s work, as well as that of many other scientists following in their footsteps, is generally referred to as quantum mechanics.<\/p>\n<div id=\"fs-idm148452752\" class=\"chemistry link-to-learning\">\n<p id=\"fs-idp90020512\">You may also have heard of Schr\u00f6dinger because of his famous thought experiment. <a href=\"http:\/\/openstaxcollege.org\/l\/16superpos\">This story<\/a> explains the concepts of superposition and entanglement as related to a cat in a box with poison.<\/p>\n<\/div>\n<\/div>\n<div id=\"fs-idp27284864\" class=\"bc-section section\">\n<h3><strong>Understanding Quantum Theory of Electrons in Atoms<\/strong><\/h3>\n<p>In our current quantum mechanical model of the atom, we can no longer accept that electrons travel in set orbits around the nucleus.\u00a0 However, we must still accept the idea of quantized energy levels, as they arose from experimental observations of actual line spectra.<\/p>\n<p>Now, we interpret the energy levels as corresponding to orbitals in the atom.\u00a0 An <strong>atomic orbital<\/strong> is interpreted as a general region in an atom within which an electron is most probable to reside.\u00a0 \u00a0But in truth, they are the wavefunctions that are solutions to the Schrodinger equation.\u00a0 These orbital wavefunctions describe the <strong>probability<\/strong> of finding an electron (<em>\u03c8<sup>2<\/sup><\/em>, as described above).<\/p>\n<p id=\"fs-idm171695728\">As before, the energy levels are labeled with an <em>n<\/em> value, where <em>n<\/em> = 1, 2, 3, \u2026. This number, <strong>n<\/strong>, is referred to as the <strong>principal quantum number<\/strong>. Generally speaking, the energy of an electron in an atom is greater for greater values of <em>n<\/em>. The principal quantum number is\u00a0 also related to the average distance the electron is from the nucleus. The positively charged protons in the nucleus stabilize the electronic orbitals by electrostatic attraction between the positive charges of the protons and the negative charges of the electrons. So the further away the electron is from the nucleus, the greater the energy it has.<\/p>\n<p id=\"fs-idm166868080\">This quantum mechanical model for where electrons reside in an atom can be used to look at electronic transitions, the events when an electron moves from one energy level to another. If the transition is to a higher energy level, energy is absorbed, and the energy change has a positive value. To obtain the amount of energy necessary for the transition to a higher energy level, a photon is absorbed by the atom. A transition to a lower energy level involves a release of energy, and the energy change is negative. This process is accompanied by emission of a photon by the atom.<\/p>\n<p id=\"fs-idm184616288\">There are certain distances from the nucleus at which the probability density of finding an electron located at a particular orbital is zero. In other words, the value of the wavefunction <em>\u03c8<\/em> is zero at this distance for this orbital. Such a value of radius <em>r<\/em> is called a <strong>node<\/strong>.<\/p>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_sOrbit\" class=\"bc-figure figure\">\n<div class=\"bc-figcaption figcaption\">The graphs show the probability (<em>y<\/em> axis) of finding an electron for the 1<em>s<\/em>, 2<em>s<\/em>, 3<em>s<\/em> orbitals as a function of distance from the nucleus.<\/div>\n<p><span id=\"fs-idm165672208\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_sorbit-1.jpg\" alt=\"This figure provides images and graphs to illustrate the probability of finding an electron in 1 s, 2 s, and 3 s orbitals as a function of the distance from the nucleus. The 1 s orbital is shown as a sphere with a chunk missing. Below it, a graph is marked on its horizontal axis at 0 and 50 p m. The related curve quickly reaches a maximum height and rapidly declines. The label, \u201c1 s\u201d appears below the graph. The 2 s orbital is shown as a red sphere with a blue middle. A chunk is missing from the sphere. A graph below it is marked on its horizontal axis at 0, 50, and 100 p m. The related curve quickly reaches a relative maximum height, a significantly higher absolute maximum height, and then rapidly declines. The label \u201c2s\u201d appears below it. The 3 s orbital is a blue sphere with a red sphere and another blue sphere at its core. A graph below it is marked on its horizontal axis at 0, 50, 100, and 150 p m. The related curve quickly reaches a relative maximum height, a second relative maximum height, a significantly higher absolute maximum, and then declines more gradually than illustrated in the previous 2 graphs. The label, \u201c3 s,\u201d appears below the graph.\" \/><\/span><\/p>\n<\/div>\n<p id=\"fs-idm158802176\">The electron density distribution of an <em>s <\/em>orbital is spherical and a <em>p<\/em> orbital has a dumbbell shape. The <em>d<\/em> and <em>f<\/em> orbitals are more complex. These shapes represent the three-dimensional regions within which the electron is likely to be found.<\/p>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_Oshapes\" class=\"bc-figure figure\">\n<div class=\"bc-figcaption figcaption\">Shapes of <em>s<\/em>, <em>p<\/em>, <em>d<\/em>, and <em>f<\/em> orbitals.<\/div>\n<p><span id=\"fs-idm313200\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_Oshapes-1.jpg\" alt=\"This diagram illustrates the shapes and quantities of all s, p, d, and f orbitals. The s sublevel is composed of a single spherical orbital. The p sublevel is composed of 3 dumbbell shaped orbitals oriented along the x, y, and z axes. The five d sublevels and seven f sublevels are considerably more complex.\" \/><\/span><\/p>\n<\/div>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_subshells\" class=\"bc-figure figure\">\n<div><\/div>\n<div class=\"bc-figcaption figcaption\">The chart shows the energies of electron orbitals in a multi-electron atom.<\/div>\n<p><span id=\"fs-idm149251120\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_subshells-1.jpg\" alt=\"This diagram shown has an upward pointing arrow at the left which is labeled \u201cE.\u201d To the right of this arrow near the bottom of the image is a single line which is labeled, \u201c1 s.\u201d Above and just to the right is another black line that is labeled, \u201c2 s.\u201d Slightly up and to the right is a grouping of three black lines labeled, \u201c2 p.\u201d Above and to the right is a single black line labeled, \u201c3 s.\u201d Slightly up and to the right is a grouping of three black lines that are labeled, \u201c3 p.\u201d Just above and to the right is a grouping of 5 black lines labeled, \u201c3 d.\u201d Slightly below and to the right is a single black line which is labeled, \u201c4 s.\u201d Just above and to the right, at a level slightly higher than the previous black lines, is a grouping of three black lines all labeled, \u201c4 p.\u201d\" \/><\/span><\/p>\n<\/div>\n<p id=\"fs-idm83747248\"><a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_subshells\">(Figure)<\/a> illustrates the energy levels for various orbitals. The number before the orbital name (such as 2<em>s<\/em>, 3<em>p<\/em>, and so forth) stands for the principal quantum number, <em>n<\/em>. The letter in the orbital name defines the sublevel: <em>s<\/em> orbitals, <em>p<\/em> orbitals, <em>d<\/em> orbitals, etc. \u00a0In the case of a hydrogen atom or a one-electron ion (such as He<sup>+<\/sup>, Li<sup>2+<\/sup>, and so on), energies of all the orbitals with the same <em>n<\/em> are the same. This is called a degeneracy, and the energy levels for the same principal quantum number, <em>n<\/em>, are called <strong>degenerate<\/strong> orbitals. However, in atoms with more than one electron, this degeneracy is eliminated by the electron\u2013electron interactions, and orbitals that belong to different sublevels have different energies, as shown on <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_subshells\">(Figure)<\/a>. Orbitals within the same sublevel are still degenerate and have the same energy.<\/p>\n<p id=\"fs-idm136117120\">So far, we have been considering the orbitals, which we interpret is the regions in space where electrons can be found.\u00a0 Now we will consider the behavior of the electrons themselves. \u00a0 In an atom, each electron acts as a tiny magnet or a tiny rotating object with an angular momentum; we describe this intrinsic electron \u201crotation\u201d in terms of a property called electron spin.<\/p>\n<p id=\"fs-idm82083456\">An electron can only \u201cspin\u201d in one of two quantized states. One is termed the \u03b1 state (&#8220;spin up&#8221;). \u00a0The other is called the \u03b2 state (&#8220;spin down&#8221;). Any electron, regardless of the atomic orbital it is located in, can only be spin up or spin down.<\/p>\n<p>&nbsp;<\/p>\n<div id=\"CNX_Chem_06_03_spin\" class=\"scaled-down\">\n<div class=\"bc-figcaption figcaption\">Electrons in an external magnetic field.<\/div>\n<p><span id=\"fs-idm7831072\"><img decoding=\"async\" src=\"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-content\/uploads\/sites\/1718\/2022\/06\/CNX_Chem_06_03_spin-1.jpg\" alt=\"This diagram has an upward pointing arrow at the left which is labeled, \u201cB subscript 0.\u201d To the right, two spheres are shown. The first has a gray square at the top labeled, \u201cN,\u201d and a second gray square at the bottom labeled, \u201cS.\u201d A curved arrow is pointing right across the surface of the sphere and a gray arrow points upward through the center of the sphere. This sphere is labeled, \u201cSpin plus one-half, spin-up.\u201d The sphere just to the right has a gray square above it labeled, \u201cS,\u201d and a gray square below it labeled, \u201cN.\u201d This sphere has a curved arrow on its surface that is directed to the left and a gray arrow through the center of the sphere that points downward. This sphere is labeled, \u201cSpin negative one-half spin-down.\u201d\" \/><\/span><\/p>\n<\/div>\n<p id=\"fs-idm91739088\"><a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_spin\">(Figure)<\/a> illustrates this phenomenon. An electron acts like a tiny magnet. Its moment is directed up (in the positive direction of the <em>z<\/em> axis) and down (in the negative <em>z<\/em> direction). A magnet has a lower energy if its magnetic moment is aligned with the external magnetic field (the left electron on <a class=\"autogenerated-content\" href=\"#CNX_Chem_06_03_spin\">(Figure)<\/a>) and a higher energy for the magnetic moment being opposite to the applied field. This is true even for an electron occupying the same orbital in an atom.<\/p>\n<\/div>\n<div id=\"fs-idm162650560\" class=\"bc-section section\">\n<h3><strong>The Pauli Exclusion Principle<\/strong><\/h3>\n<p id=\"fs-idm225354640\">Now that we have looked at the orbitals and the electrons separately, we are ready to consider how electrons are placed in orbitals within an atom.\u00a0 \u00a0The <strong>Pauli exclusion principle, <\/strong>named for an Austrian physicist Wolfgang Pauli, can be formulated as follows: no two electrons in the same orbital can have the same spin.\u00a0 Since there are only two spin states, any atomic orbital can be populated by only zero, one, or two electrons.<\/p>\n<div id=\"fs-idm169030688\" class=\"textbox textbox--examples\">\n<p id=\"fs-idm68824256\"><strong>Maximum Number of Electrons:<\/strong><\/p>\n<p>Calculate the maximum number of electrons that can occupy an energy level with (a) <em>n<\/em> = 2, (b) <em>n<\/em> = 5, and (c) <em>n<\/em> as a variable. Note you are only looking at the orbitals with the specified <em>n<\/em> value, not those at lower energies.<\/p>\n<p id=\"fs-idm174701168\"><strong>Solution:<\/strong><\/p>\n<p>(a) When <em>n<\/em> = 2, there are four orbitals (a single 2<em>s<\/em> orbital, and three orbitals labeled 2<em>p<\/em>). These four orbitals can contain eight electrons.<\/p>\n<p id=\"fs-idm146693328\">(b) When <em>n<\/em> = 5, there are five sublevels of orbitals that we need to sum:<\/p>\n<div id=\"fs-idm204408304\" style=\"text-align: center\">1 orbital labelled 5<em>s<\/em><\/div>\n<div style=\"text-align: center\">3 orbitals labelled 5<em>p<\/em><\/div>\n<div style=\"text-align: center\">5 orbitals labelled 5<em>d<\/em><\/div>\n<div style=\"text-align: center\">7 orbitals labelled 5<em>f<\/em><\/div>\n<div style=\"text-align: center\"><span style=\"text-decoration: underline\">9 orbitals labelled 5<em>g<\/em><\/span><\/div>\n<div style=\"text-align: center\">25 orbitals total<\/div>\n<div><\/div>\n<p id=\"fs-idm145553968\">Again, each orbital holds two electrons, so 50 electrons can fit in this energy level.<\/p>\n<p id=\"fs-idm106652512\">(c) The number of orbitals in any energy level <em>n<\/em> will equal <em>n<\/em><sup>2<\/sup><sub>.<\/sub> There can be up to two electrons in each orbital, so the maximum number of electrons will be 2<em>n<\/em><sup>2<\/sup>.<\/p>\n<p id=\"fs-idm13201440\"><strong>Check Your Learning:<\/strong><\/p>\n<p>If an energy level contains a maximum of 32 electrons, what is the principal quantum number, <em>n<\/em>?<\/p>\n<p>&nbsp;<\/p>\n<div id=\"fs-idm166820736\">\n<div><strong>Answer:<\/strong><\/div>\n<p id=\"fs-idm135023952\"><em>n<\/em> = 4<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"fs-idm55472464\" class=\"summary\">\n<h3><strong>Key Concepts and Summary<\/strong><\/h3>\n<p id=\"fs-idm175984864\">Macroscopic objects act as particles. Microscopic objects (such as electrons) have properties of both a particle and a wave. Their exact trajectories cannot be determined. The quantum mechanical model of atoms describes the three-dimensional position of the electron in a <em>probabilistic<\/em> manner according to a mathematical function called a wavefunction, often denoted as <em>\u03c8<\/em>. Atomic wavefunctions are also called orbitals. The squared magnitude of the wavefunction describes the distribution of the probability of finding the electron in a particular region in space. Therefore, atomic orbitals describe where electrons in an atom are most likely to be found.<\/p>\n<\/div>\n<div id=\"fs-idm162744496\" class=\"exercises\">\n<div id=\"fs-idm24126560\">\n<div id=\"fs-idm29306320\"><\/div>\n<\/div>\n<\/div>\n<div class=\"textbox shaded\">\n<h3><strong>Glossary<\/strong><\/h3>\n<dl id=\"fs-idm176142304\">\n<dt>secondary (angular momentum) quantum number (<em>l<\/em>)<\/dt>\n<dd id=\"fs-idm128619824\">quantum number distinguishing the different shapes of orbitals; it is also a measure of the orbital angular momentum<\/dd>\n<\/dl>\n<dl id=\"fs-idm147438368\">\n<dt>atomic orbital<\/dt>\n<dd id=\"fs-idm109054128\">mathematical function that describes the behavior of an electron in an atom (also called the wavefunction)<\/dd>\n<\/dl>\n<dl id=\"fs-idp12032\">\n<dt><em>d<\/em> orbital<\/dt>\n<dd id=\"fs-idm164271760\">region of space with high electron density that is either four lobed or contains a dumbbell and torus shape; describes orbitals with <em>l<\/em> = 2.<\/dd>\n<\/dl>\n<dl id=\"fs-idm442273488\">\n<dt>degenerate orbitals<\/dt>\n<dd id=\"fs-idm476031024\">orbitals that have the same energy<\/dd>\n<\/dl>\n<dl id=\"fs-idm56391008\">\n<dt>electron density<\/dt>\n<dd id=\"fs-idp58829584\">a measure of the probability of locating an electron in a particular region of space, it is equal to the squared absolute value of the wave function <em>\u03c8<\/em><\/dd>\n<\/dl>\n<dl id=\"fs-idm174396336\">\n<dt>energy level<\/dt>\n<dd id=\"fs-idm12350992\">atomic orbitals with the same principal quantum number, <em>n<\/em><\/dd>\n<\/dl>\n<dl id=\"fs-idm166903488\">\n<dt>magnetic quantum number (<em>m<sub>l<\/sub><\/em>)<\/dt>\n<dd id=\"fs-idm147105616\">quantum number signifying the orientation of an atomic orbital around the nucleus<\/dd>\n<\/dl>\n<dl id=\"fs-idm147658080\">\n<dt><em>p<\/em> orbital<\/dt>\n<dd id=\"fs-idm165030336\">dumbbell-shaped region of space with high electron density, describes orbitals with <em>l<\/em> = 1<\/dd>\n<\/dl>\n<dl id=\"fs-idm120400016\">\n<dt>Pauli exclusion principle<\/dt>\n<dd id=\"fs-idp43763072\">specifies that no two electrons in an atom can have the same value for all four quantum numbers<\/dd>\n<\/dl>\n<dl id=\"fs-idm140352128\">\n<dt>principal quantum number (<em>n<\/em>)<\/dt>\n<dd id=\"fs-idm13159072\">quantum number specifying the energy level an electron occupies in an atom<\/dd>\n<\/dl>\n<dl id=\"fs-idm160875424\">\n<dt>quantum mechanics<\/dt>\n<dd id=\"fs-idm48323504\">field of study that includes quantization of energy and wave-particle duality to describe matter<\/dd>\n<\/dl>\n<dl id=\"fs-idm144189680\">\n<dt><em>s<\/em> orbital<\/dt>\n<dd id=\"fs-idm168786512\">spherical region of space with high electron density, describes orbitals with <em>l<\/em> = 0<\/dd>\n<\/dl>\n<dl>\n<dd><\/dd>\n<\/dl>\n<dl id=\"fs-idm137493808\">\n<dt>spin quantum number (<em>m<sub>s<\/sub><\/em>)<\/dt>\n<dd id=\"fs-idm165810304\">number specifying the electron spin direction, either \u00bd or -\u00bd<\/dd>\n<\/dl>\n<dl id=\"fs-idm148470816\">\n<dt>sublevel<\/dt>\n<dd id=\"fs-idm136103056\">atomic orbitals with the same values of <em>n<\/em> and <em>l<\/em><\/dd>\n<\/dl>\n<dl id=\"fs-idm163956768\">\n<dt>wavefunction (<em>\u03c8<\/em>)<\/dt>\n<dd id=\"fs-idm106660816\">mathematical description of an atomic orbital that describes the shape of the orbital; it can be used to calculate the probability of finding the electron at any given location in the orbital, as well as dynamical variables such as the energy and the angular momentum<\/dd>\n<\/dl>\n<\/div>\n<p>&lt;!&#8211; pb_fixme &#8211;&gt;<\/p>\n<\/div>\n<div>&lt;!&#8211; pb_fixme &#8211;&gt;&lt;!&#8211; pb_fixme &#8211;&gt;<\/div>\n","protected":false},"author":1392,"menu_order":39,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[49],"contributor":[],"license":[],"class_list":["post-415","chapter","type-chapter","status-publish","hentry","chapter-type-numberless"],"part":1393,"_links":{"self":[{"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/chapters\/415","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/wp\/v2\/users\/1392"}],"version-history":[{"count":3,"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/chapters\/415\/revisions"}],"predecessor-version":[{"id":1548,"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/chapters\/415\/revisions\/1548"}],"part":[{"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/parts\/1393"}],"metadata":[{"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/chapters\/415\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/wp\/v2\/media?parent=415"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/pressbooks\/v2\/chapter-type?post=415"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/wp\/v2\/contributor?post=415"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/chemistry2eengineering\/wp-json\/wp\/v2\/license?post=415"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}