Orbitals, the Basics: Atomic Orbital Tutorial — probability, shapes, energy |Crash Chemistry Academy

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That's the common way to do it or am I missing something?

👍︎︎ 31 👤︎︎ u/FalconX88 📅︎︎ Jan 13 2018 🗫︎ replies

I like how he shows multiple types of orbitals overlaid in the same space (like the 1s 2s and 2p). A lot of texts and lectures describe them completely separately and fail to connect with students how intertwined they are. It makes it harder for folks to understand hybridized orbitals later on (like sp2 with character from the overlapping s and p orbitals contributing to the whole MO).

👍︎︎ 11 👤︎︎ u/TheWoolyGoat 📅︎︎ Jan 13 2018 🗫︎ replies

Good video, nice explanation for the introductory chemistry student, but I don't like how he says not to worry about why the orbitals have the shapes that they do.

I understand that it's not necessary to know why orbitals are shaped the way they are for the purposes of general chemistry but saying that makes the shapes seem as if they are arbitrary/don't follow a pattern.

Understanding why orbitals have a particular shape and how their shape relates to their energy level helps you understand the wave nature of electrons more deeply, which is a key insight to understanding things like MO theory in my opinion.

👍︎︎ 11 👤︎︎ u/Try_DMT 📅︎︎ Jan 13 2018 🗫︎ replies

One of my biggest pet peeves is that atomic orbitals are often not stated to be an approximation. In reality there is only one wavefunction for the ground state of the entire atom: the lowest energy solution to the Schrodinger equation for the given system. Unfortunately, for all but the lightest atoms, this PDE has too many variables to be tractable, so approximations are used to solve it.

The orbitals are defined under the approximation that the electrons are independent and moving in the same average potential (found using the Hartree-Fock method), so each is a different solution to the Schrodinger equation. The total ground state wavefunction of the atom is approximated as the product of all the orbitals (or, better, an antisymmetrization of them).

It's a good approximation, but IMO it needs to be stated. It seems to cause misconceptions that persist for years. The method also has limitations that should be explained.

👍︎︎ 3 👤︎︎ u/[deleted] 📅︎︎ Jan 14 2018 🗫︎ replies

Does the orbital describe a "planar" boundary where the inside is hollow? Or is the electron just as likely to be found on the inside as on the surface?

👍︎︎ 1 👤︎︎ u/heyandy889 📅︎︎ Jan 13 2018 🗫︎ replies

I wish i had this last semester when I was in gen chem. I didn't understand that they all fit together like this. My mind is a bit blown I must say!

👍︎︎ 1 👤︎︎ u/alyssa1221 📅︎︎ Jan 14 2018 🗫︎ replies

I want to ask you all this one thing, was orbitals, in any way, taught to you in highschool? I live in Turkey and orbitals were first taught at 11th grade, currently studying for the university exam, and I have to study all these and their calculations and I don't really know much about how the rest of the world handles highschool science classes.

👍︎︎ 1 👤︎︎ u/[deleted] 📅︎︎ Jan 14 2018 🗫︎ replies

I could have used this last semester 😥

👍︎︎ 1 👤︎︎ u/Rotoscope8 📅︎︎ Jan 14 2018 🗫︎ replies
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This tutorial is about orbitals. We're going to look at what orbitals are, what they represent, how electrons go in orbitals, the order electrons go in orbitals, and the shapes of orbitals. So we know that atoms are made out of electrons, protons, and neutrons. Electrons are very important. The arrangement of electrons dictates how atoms will interact with each other. But we don't really know where electrons are inside an atom. We can define areas where they are with some high probability, but we can never really know exactly where they are. And so we define these areas as orbitals: It is "high probability" that is the operative idea. We don't know where electrons are going to be all the time, but we know where they are going to be 90% of the time. That's what is meant when we say that the probability of these orbitals are "probability clouds." Let's talk, before we go any further, about the word "orbitals." It's an unfortunate word. It comes from the word "orbit" which came from Bohr's idea that electrons orbit the nucleus like planets orbit the sun. And we know that electrons do not orbit the nucleus. And so the word "orbitals" is sometimes a word that can create a misconception with students. It makes students think that electrons orbit the nucleus, and they do not. We only can know with a certain amount of probability, 90%, where an electron might be, but not the path that it's taking. And that come's from Heisenberg's "uncertainty principle." As I said, this is important, because: Schrödinger, building on Heisenberg's uncertainty principle, as well as De Broglie's idea that electrons can act as waves, Schrödinger created a mathematical model that described these orbitals inside an atom, these shapes, these high probability clouds. But we cannot know precisely where the electrons are inside the orbitals, and again, that comes from Heisenberg's uncertainty principle. So we're going to take a look at that three dimensional space. We're going to define it with the three axises, x,y,z. The intersection of which will be our nucleus. Our first orbital is going to be the "1s" orbital. And what we're going to do now, is take a look at the shapes of orbitals and what they're called. They're always designated with a number and a letter. The letter designates the shape and there number designates the energy level. So the 1s orbital is the lowest energy orbital. And the electrons in the 1s orbital are the lowest energy electrons. The problem is, the orbitals can only hold a maximum of two electrons. So if we were talking about helium with two electrons, that would be fine. Helium would be happy with the 1s orbital. But what if we were talking about Lithium? Lithium has three electrons. Where would the third electron go? Well... It would go in the next higher energy level orbital, which is the "2s" orbital. Notice that we still have an "s" orbital and that we still have a spherical shape. But the electrons in the 2s orbital are higher energy. And so therefore, on average, they're going to be further from the nucleus which describes therefore a larger shape, a larger area that they're going to occupy. But again, this is just a single orbital. It can also hold two electrons. We still have the 1s orbital inside of it holding two electrons. So with the two orbitals we have now, we can have a maximum of four electrons. That brings us to Beryllium [Be]. Beryllium is happy with the 1s and the 2s orbital. But what about Boron [B]? Boron has five electrons! Where is the fifth electron going to go? So as you may have guessed, we're going to go another orbital, a higher energy orbital. [And just to review, we have the 1s orbital which has two electrons, we have the 2s orbital that has two electrons.] [And don't forget, the orbital is the shape of the space where there is a high probability of finding electrons and "s" orbitals are spheres.] And so what about that fifth electron? The fifth electron is going to start filling the "2p" orbitals. So here we have a different shape. We have the "p" shape. There are three 2p orbitals and they are all oriented perpendicular to each other. So we have the pinkish red on the y axis. That's one orbital. Here's the second orbital, along the x axis, that's greenish yellow, I guess. And then the third 2p orbital along the z axis. Each orbital, as you can see, consists of two lobes. So both lobes together constitute just one orbital and can only hold a maximum of two electrons So we designate each individual orbital by the axis it's on. So here the 2p orbital would be called 2p y, 2p x, and 2p z. We cannot forget that the orbital that the orbital is the shape of the space where there is a high probability of finding electrons. And P orbitals could be called a "dumbbell" shape, they have two lobes. So let's say that fifth electron of Boron [B] goes into 2p. But what if we need to accommodate a sixth electron, like with carbon [C]? Carbon has a total of 6 electrons. Well, that electron could go into the 2p z orbital. And then, what about Nitrogen [N]? The seventh electron that Nitrogen has can go into the 2p y orbital. But we said that each orbital can have a maximum of two electrons. So, once each one of these orbitals has one electron, then they can start to pair up and fill each orbital with a total of two electrons. And that would give the three 2p orbitals a total of six electrons. The p orbitals are filling up. We know that the 1s and the 2s must also be filled up. So let's take a look at that. Once the 1s orbital is filled, we can then start to fill the 2s orbital—but again with only two electrons. Once 2s is filled, and remember 1s is still there, it hasn't disappeared. So 2s fills around the 1s. But now, once 2s is filled, we start to fill 2p. Again, the 2s, the 1s, they're still in existence. So therefore the p orbitals actually overlap with the 1s and 2s orbitals. So here's one of the 2p orbitals. Once another electron would come and fill this 2p orbital, another electron would come and fill this 2p orbital. Let's say all these orbitals are completely filled, and therefore we would have the 1s orbital with two electrons. We would have 2s orbital with two electrons, and we would have the 2p orbitals with six electrons. How many electrons total is that? 10 electrons. What element has 10 electrons? Neon [Ne]. If all of these orbitals are filled up, that would be 10 electrons, and that would be Neon. But what about Sodium [Na]? Sodium has 11 electrons. Where would that 11th electron go? As you might have guessed, it would go in the next highest energy level, the next highest orbital. And that would be... "3s"! 3s has electrons that have higher energy than any of those other orbitals we looked at and so therefore its electrons on average are further from the nucleus than the others. And it is larger than 1s, 2s, or 2p orbitals, and surrounds them. So we can see the other orbitals still exist inside the 3s orbital and the 3s orbital with Sodium now is able to start getting electrons. So there's many more elements and there are other orbitals as well. So let's take a look at the other orbitals. First lets review: The s orbital is spherical. There's only a single s orbital at any one energy level. There's the three p orbitals with this shape. There are five d-orbitals. And this is their shape. Each one of these is a single orbital. And each one of these can have at most two electrons. The illustration describes the outer boundary of that 90 percent probability of where the electron is going to be. So that outer boundary, that surface, plus all the space inside of it constitutes the 90 percent area where we are going to find and electron in a d-orbital. And then there is one more, the f-orbitals, and there are seven of them. Again, each one of them is a single orbital and each one of them can have a maximum of two electrons. So the electrons can be anywhere, they're traveling 90 percent of the time, anywhere inside these lobes. And if you track the electron long enough, you will start to see and describe these exact shapes that we're seeing here. One thing I think students can get confused with is these shapes and what they represent, especially when they get as complicated as the d and the f-orbitals, and there is even the g-orbitals that are even more complicated than the f-orbitals. So don't get tripped up by the complicated shapes. All you need to understand is what they represent. And they simply represent space inside of which you are going to find the electron 90 percent of the time. So you don't have to worry about the specific shape so much, just know what these shapes represent: where the electron is going to be. So finally, a nice way to look at that is this schematic. Energy is shown increasing on the y axis, and each orbital is represented as a circle. The circles don't represent the shape of the orbital, they're just representing the existence of the orbital. So at any one energy level, what was always just a single s orbital. And so the s-orbitals, as you go to 1s, 2s, 3s, 4s etc, they keep increasing in energy. As we saw before, 2p orbitals are higher in energy than 2s and there are three of them. So the three circles represent the three 2p orbitals—not the shape, just the fact that there are three orbitals within the 2p energy level. The 3p energy level, again p always just has three orbitals. But what about d? We saw before that there are five d orbitals. So at any energy level which has d-orbitals, there's always going to be five of them at that energy level. And then finally, f-orbitals, there are seven of them. So any energy level that has f-orbitals is going to have seven of them as long as there are electrons to fill those orbitals. The orbital does not exist unless the electron is in the orbital. So "what," might you ask, "does that have to do with anything? Why do we care about how electrons are arranged in an atom?" Well, atoms are constantly interacting around you, on the earth, in the solar system, in the universe. Those interactions depend on how electrons are arranged in each atom. That arrangement, its orbitals, determine how the atoms interact with other atoms. If atoms did not interact with each other, would you be sitting here reading this? Probably not.
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Channel: Crash Chemistry Academy
Views: 1,342,092
Rating: 4.8565083 out of 5
Keywords: d orbitals, orbital filling, find, easy, beginners, calculate, quantum numbers, table, math, energy levels, f orbitals, valence, explained, orbital, tutorial, p orbitals, filling, course, periodic, orbitals, metallic, crash, how to, covalent, practice, volume, electron configuration, experiment, s p d f, organic, nodes, subshells, shells, animation, academy, bonding, step by step, video, s orbitals, problems, orbital shapes, s-orbital, chemistry
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Length: 14min 28sec (868 seconds)
Published: Mon Aug 01 2011
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