INSTRUCTOR: Heisenberg's uncertainty principle is one of the most important and fundamental principles in our understanding of atomic theory. However, Heisenberg uncertainty principle is also very difficult to get a conceptual understanding or a physical feel for how to use it and how it gets expressed in real chemical systems. So Heisenberg uncertainty principle is often expressed mathematically in terms of this equation, where delta x represents the uncertainty and position, delta p represents the uncertainty of momentum, and the product of those two always has to be greater than or equal to Planck's constant h divided by 4 pi. So in this case, if you know the position well, then you can't know the momentum very well or the velocity. And vise versa. If you know the momentum or the velocity well for a particle, you're not going to know the position very well. But again, how does that get expressed in real physical systems? So in this case, we're going to demonstrate this using another virtual experiment in virtual chem lab, where we're going to perform the two-slit diffraction experiment. In the two-slit diffraction experiment, we have a laser. And this laser we're able to tune or adjust the wavelength to anything that we want. In this case, we've adjusted it to 500 nanometers. And we can also control the power or the intensity of the light coming out of the laser. We have here a two-slit device. Now this is virtual. It's actually difficult to do this in a real experiment. But in this case, we have two infinitely long splits spaced, in this case, 3 microns apart or 3 times 10 to the minus 6 meters or 3 times 10 to the minus 3 millimeters. And we're going to detect the light using this video camera. So in this case, this video camera, the output of this video camera is going to be shown here in this screen as well. So in this case, we have 500 nanometer light, the intensity is 1 nano Watt or considerably pretty high going through two slits that are spaced at 3 microns, and we're going to see what happens here. In this case, you notice that there are these light spots and dark spots. This is caused by constructive and destructive interference. What is the cause of this dark spot region right here? We can understand constructive and destructive interference in terms of light waves. So if we assume the light is coming out as a wave, you can think of constructive interference or these light regions as where the light adds together and gives us an enhanced brighter signal. And the dark region is where the light comes together and subtracts, or one wave subtracts from another and gives us a dark region. So you can see that this is pretty clearly we can treat light as a wave. It behaves like a wave. It gives us diffraction patterns. It gives us constructive and destructive interference. But now the question becomes, what's going to happen if we change the intensity of the light? What if we turn it down and we only have a single photon at a time going through the two slits? So you remember when we had a lot of light, we had lots of photons. And we can imagine those interacting with each other. But what's going to happen if I turn down this laser and I only get one photon at a time in the slits? What's going to change, if anything? So let's go do this experiment and see what the answer is. So we're going to turn down the intensity of our laser, and turn it down to 100 photons per second. So imagine that we have a single photon in the slits at a time. So imagine that we have 100 photons in a line coming through the slit at any one time. But only one photon is in the slit. So there's nothing for it to interact. We see something quite different. We don't see a diffraction pattern. And we see these individual photon hits on our detector screen here. So notice that you can't predict where any one photon is going to hit. It could be here, it could be over there. You can kind of see that they're congregated in the middle, but there's no really way to predict where each photon is going to hit when we have individuals. So perhaps the answer is that we have a very different experiment now because we only have single photons in the slits. Let's go do something virtual. And let's save where all these photons hit the screen. So we'll click on that persist button, and save where it hits. And you notice that over time, you start building up and you start seeing a diffraction pattern again. So that's really interesting. We only have a single photon in those slits at a time, but how do we get diffraction if it has no other photons for it to interact with? Well, this is another expression or a better expression of Heisenberg's uncertainty principle. Notice that we had single photons, we couldn't predict where it was going to go. Our uncertainty was very high in the position because we knew the wavelength. So therefore, we knew its momentum well. So we knew the momentum, but we didn't know its position. So we couldn't predict where that photon was going to hit. But if I save over time, and get good statistics. So I have lots of photons saved over time, then I can start seeing what that pattern is going to be. And I'm going to get that diffraction pattern. In the first experiment where I had high intensity, I had lots of photons. Lots of statistics. My statistics were high, my probability was high. So I could see a diffraction pattern. So both experiments turned out to be the same, one was just an expression of Heisenberg's uncertainty principle, and that I didn't know its position. So when it comes to the atom, same idea. When we have a single atom with a few electrons floating around it, we don't know-- we don't have good statistics. We can't predict where that electron is going to be. So we talk about probability. But when we have lots of atoms and lots of interactions going on, we got great statistics. And so our predictive ability is better.
Table of contents
- 1. Intro to General Chemistry3h 46m
- Classification of Matter16m
- Physical & Chemical Changes19m
- Chemical Properties7m
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- 2. Atoms & Elements4h 16m
- The Atom9m
- Subatomic Particles15m
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- Ions27m
- Atomic Mass28m
- Periodic Table: Classifications11m
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- 4. BONUS: Lab Techniques and Procedures1h 38m
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- 9. Quantum Mechanics2h 58m
- Wavelength and Frequency6m
- Speed of Light8m
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- Electromagnetic Spectrum10m
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- De Broglie Wavelength9m
- Heisenberg Uncertainty Principle17m
- Bohr Model14m
- Emission Spectrum5m
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- Introduction to Quantum Mechanics5m
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- 10. Periodic Properties of the Elements3h 10m
- The Electron Configuration22m
- The Electron Configuration: Condensed4m
- The Electron Configurations: Exceptions13m
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- Paramagnetism and Diamagnetism9m
- The Electron Configuration: Quantum Numbers16m
- Valence Electrons of Elements12m
- Periodic Trend: Metallic Character3m
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- 11. Bonding & Molecular Structure3h 29m
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- 12. Molecular Shapes & Valence Bond Theory1h 57m
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- Molecular Polarity10m
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- 15. Chemical Kinetics2h 53m
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- 17. Acid and Base Equilibrium5h 1m
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- Oxyacids10m
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- Amphoteric Species5m
- Arrhenius Acids and Bases5m
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- pH of Weak Bases32m
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- 18. Aqueous Equilibrium4h 47m
- Intro to Buffers20m
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- Titrations: Weak Acid-Strong Base38m
- Titrations: Weak Base-Strong Acid41m
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- Titrations: Diprotic & Polyprotic Buffers32m
- Solubility Product Constant: Ksp17m
- Ksp: Common Ion Effect18m
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- 19. Chemical Thermodynamics1h 50m
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- 21. Nuclear Chemistry2h 34m
- Intro to Radioactivity10m
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- Electron Capture & Positron Emission8m
- Neutron to Proton Ratio7m
- Band of Stability: Alpha Decay & Nuclear Fission10m
- Band of Stability: Beta Decay3m
- Band of Stability: Electron Capture & Positron Emission4m
- Band of Stability: Overview14m
- Measuring Radioactivity7m
- Rate of Radioactive Decay12m
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- Mass Defect18m
- Nuclear Binding Energy14m
- 22. Organic Chemistry5h 7m
- Introduction to Organic Chemistry8m
- Structural Formula8m
- Condensed Formula10m
- Skeletal Formula6m
- Spatial Orientation of Bonds3m
- Intro to Hydrocarbons16m
- Isomers11m
- Chirality15m
- Functional Groups in Chemistry11m
- Naming Alkanes4m
- The Alkyl Groups9m
- Naming Alkanes with Substituents13m
- Naming Cyclic Alkanes6m
- Naming Other Substituents8m
- Naming Alcohols11m
- Naming Alkenes11m
- Naming Alkynes9m
- Naming Ketones5m
- Naming Aldehydes5m
- Naming Carboxylic Acids4m
- Naming Esters8m
- Naming Ethers5m
- Naming Amines5m
- Naming Benzene7m
- Alkane Reactions7m
- Intro to Addition Reactions4m
- Halogenation Reactions4m
- Hydrogenation Reactions3m
- Hydrohalogenation Reactions7m
- Alcohol Reactions: Substitution Reactions4m
- Alcohol Reactions: Dehydration Reactions9m
- Intro to Redox Reactions8m
- Alcohol Reactions: Oxidation Reactions7m
- Aldehydes and Ketones Reactions6m
- Ester Reactions: Esterification4m
- Ester Reactions: Saponification3m
- Carboxylic Acid Reactions4m
- Amine Reactions3m
- Amide Formation4m
- Benzene Reactions10m
- 23. Chemistry of the Nonmetals2h 39m
- Main Group Elements: Bonding Types4m
- Main Group Elements: Boiling & Melting Points7m
- Main Group Elements: Density11m
- Main Group Elements: Periodic Trends7m
- The Electron Configuration Review16m
- Periodic Table Charges Review20m
- Hydrogen Isotopes4m
- Hydrogen Compounds11m
- Production of Hydrogen8m
- Group 1A and 2A Reactions7m
- Boron Family Reactions7m
- Boron Family: Borane7m
- Borane Reactions7m
- Nitrogen Family Reactions12m
- Oxides, Peroxides, and Superoxides12m
- Oxide Reactions4m
- Peroxide and Superoxide Reactions6m
- Noble Gas Compounds3m
- 24. Transition Metals and Coordination Compounds3h 16m
- Atomic Radius & Density of Transition Metals11m
- Electron Configurations of Transition Metals7m
- Electron Configurations of Transition Metals: Exceptions11m
- Paramagnetism and Diamagnetism10m
- Ligands10m
- Complex Ions5m
- Coordination Complexes7m
- Classification of Ligands11m
- Coordination Numbers & Geometry9m
- Naming Coordination Compounds22m
- Writing Formulas of Coordination Compounds8m
- Isomerism in Coordination Complexes14m
- Orientations of D Orbitals4m
- Intro to Crystal Field Theory10m
- Crystal Field Theory: Octahedral Complexes5m
- Crystal Field Theory: Tetrahedral Complexes4m
- Crystal Field Theory: Square Planar Complexes4m
- Crystal Field Theory Summary8m
- Magnetic Properties of Complex Ions9m
- Strong-Field vs Weak-Field Ligands6m
- Magnetic Properties of Complex Ions: Octahedral Complexes11m
9. Quantum Mechanics
Heisenberg Uncertainty Principle
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