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Raffi Hovasapian

Vapor Pressure & Changes of State

Slide Duration:Table of Contents

I. Review

Naming Compounds

41m 24s

- Intro0:00
- Periodic Table of Elements0:15
- Naming Compounds3:13
- Definition and Examples of Ions3:14
- Ionic (Symbol to Name): NaCl5:23
- Ionic (Name to Symbol): Calcium Oxide7:58
- Ionic - Polyatoms Anions: Examples12:45
- Ionic - Polyatoms Anions (Symbol to Name): KClO14:50
- Ionic - Polyatoms Anions (Name to Symbol): Potassium Phosphate15:49
- Ionic Compounds Involving Transition Metals (Symbol to Name): Co₂(CO₃)₃20:48
- Ionic Compounds Involving Transition Metals (Name to Symbol): Palladium 2 Acetate22:44
- Naming Covalent Compounds (Symbol to Name): CO26:21
- Naming Covalent Compounds (Name to Symbol): Nitrogen Trifluoride27:34
- Naming Covalent Compounds (Name to Symbol): Dichlorine Monoxide27:57
- Naming Acids Introduction28:11
- Naming Acids (Name to Symbol): Chlorous Acid35:08
- % Composition by Mass Example37:38

Stoichiometry

37m 19s

- Intro0:00
- Stoichiometry0:25
- Introduction to Stoichiometry0:26
- Example 15:03
- Example 210:17
- Example 315:09
- Example 424:02
- Example 5: Questions28:11
- Example 5: Part A - Limiting Reactant30:30
- Example 5: Part B32:27
- Example 5: Part C35:00

II. Aqueous Reactions & Stoichiometry

Precipitation Reactions

31m 14s

- Intro0:00
- Precipitation Reactions0:53
- Dissociation of ionic Compounds0:54
- Solubility Guidelines for ionic Compounds: Soluble Ionic Compounds8:15
- Solubility Guidelines for ionic Compounds: Insoluble ionic Compounds12:56
- Precipitation Reactions14:08
- Example 1: Mixing a Solution of BaCl₂ & K₂SO₄21:21
- Example 2: Mixing a Solution of Mg(NO₃)₂ & KI26:10

Acid-Base Reactions

43m 21s

- Intro0:00
- Acid-Base Reactions1:00
- Introduction to Acid: Monoprotic Acid and Polyprotic Acid1:01
- Introduction to Base8:28
- Neutralization11:45
- Example 116:17
- Example 221:55
- Molarity24:50
- Example 326:50
- Example 430:01
- Example 4: Limiting Reactant37:51
- Example 4: Reaction Part40:01

Oxidation Reduction Reactions

47m 58s

- Intro0:00
- Oxidation Reduction Reactions0:26
- Oxidation and Reduction Overview0:27
- How Can One Tell Whether Oxidation-Reduction has Taken Place?7:13
- Rules for Assigning Oxidation State: Number 111:22
- Rules for Assigning Oxidation State: Number 212:46
- Rules for Assigning Oxidation State: Number 313:25
- Rules for Assigning Oxidation State: Number 414:50
- Rules for Assigning Oxidation State: Number 515:41
- Rules for Assigning Oxidation State: Number 617:00
- Example 1: Determine the Oxidation State of Sulfur in the Following Compounds18:20
- Activity Series and Reduction Properties25:32
- Activity Series and Reduction Properties25:33
- Example 2: Write the Balance Molecular, Total Ionic, and Net Ionic Equations for Al + HCl31:37
- Example 334:25
- Example 437:55

Stoichiometry Examples

31m 50s

- Intro0:00
- Stoichiometry Example 10:36
- Example 1: Question and Answer0:37
- Stoichiometry Example 26:57
- Example 2: Questions6:58
- Example 2: Part A Solution12:16
- Example 2: Part B Solution13:05
- Example 2: Part C Solution14:00
- Example 2: Part D Solution14:38
- Stoichiometry Example 317:56
- Example 3: Questions17:57
- Example 3: Part A Solution19:51
- Example 3: Part B Solution21:43
- Example 3: Part C Solution26:46

III. Gases

Pressure, Gas Laws, & The Ideal Gas Equation

49m 40s

- Intro0:00
- Pressure0:22
- Pressure Overview0:23
- Torricelli: Barometer4:35
- Measuring Gas Pressure in a Container7:49
- Boyle's Law12:40
- Example 116:56
- Gas Laws21:18
- Gas Laws21:19
- Avogadro's Law26:16
- Example 231:47
- Ideal Gas Equation38:20
- Standard Temperature and Pressure (STP)38:21
- Example 340:43

Partial Pressure, Mol Fraction, & Vapor Pressure

32m

- Intro0:00
- Gases0:27
- Gases0:28
- Mole Fractions5:52
- Vapor Pressure8:22
- Example 113:25
- Example 222:45

Kinetic Molecular Theory and Real Gases

31m 58s

- Intro0:00
- Kinetic Molecular Theory and Real Gases0:45
- Kinetic Molecular Theory 10:46
- Kinetic Molecular Theory 24:23
- Kinetic Molecular Theory 35:42
- Kinetic Molecular Theory 46:27
- Equations7:52
- Effusion11:15
- Diffusion13:30
- Example 119:54
- Example 223:23
- Example 326:45

AP Practice for Gases

25m 34s

- Intro0:00
- Example 10:34
- Example 10:35
- Example 26:15
- Example 2: Part A6:16
- Example 2: Part B8:46
- Example 2: Part C10:30
- Example 2: Part D11:15
- Example 2: Part E12:20
- Example 2: Part F13:22
- Example 314:45
- Example 314:46
- Example 418:16
- Example 418:17
- Example 521:04
- Example 521:05

IV. Thermochemistry

Energy, Heat, and Work

37m 32s

- Intro0:00
- Thermochemistry0:25
- Temperature and Heat0:26
- Work3:07
- System, Surroundings, Exothermic Process, and Endothermic Process8:19
- Work & Gas: Expansion and Compression16:30
- Example 124:41
- Example 227:47
- Example 331:58

Enthalpy & Hess's Law

32m 34s

- Intro0:00
- Thermochemistry1:43
- Defining Enthalpy & Hess's Law1:44
- Example 16:48
- State Function13:11
- Example 217:15
- Example 324:09

Standard Enthalpies of Formation

23m 9s

- Intro0:00
- Thermochemistry1:04
- Standard Enthalpy of Formation: Definition & Equation1:05
- ∆H of Formation10:00
- Example 111:22
- Example 219:00

Calorimetry

39m 28s

- Intro0:00
- Thermochemistry0:21
- Heat Capacity0:22
- Molar Heat Capacity4:44
- Constant Pressure Calorimetry5:50
- Example 112:24
- Constant Volume Calorimetry21:54
- Example 224:40
- Example 331:03

V. Kinetics

Reaction Rates and Rate Laws

36m 24s

- Intro0:00
- Kinetics2:18
- Rate: 2 NO₂ (g) → 2NO (g) + O₂ (g)2:19
- Reaction Rates Graph7:25
- Time Interval & Average Rate13:13
- Instantaneous Rate15:13
- Rate of Reaction is Proportional to Some Power of the Reactant Concentrations23:49
- Example 127:19

Method of Initial Rates

30m 48s

- Intro0:00
- Kinetics0:33
- Rate0:34
- Idea2:24
- Example 1: NH₄⁺ + NO₂⁻ → NO₂ (g) + 2 H₂O5:36
- Example 2: BrO₃⁻ + 5 Br⁻ + 6 H⁺ → 3 Br₂ + 3 H₂O19:29

Integrated Rate Law & Reaction Half-Life

32m 17s

- Intro0:00
- Kinetics0:52
- Integrated Rate Law0:53
- Example 16:26
- Example 215:19
- Half-life of a Reaction20:40
- Example 3: Part A25:41
- Example 3: Part B28:01

Second Order & Zero-Order Rate Laws

26m 40s

- Intro0:00
- Kinetics0:22
- Second Order0:23
- Example 16:08
- Zero-Order16:36
- Summary for the Kinetics Associated with the Reaction21:27

Activation Energy & Arrhenius Equation

40m 59s

- Intro0:00
- Kinetics0:53
- Rate Constant0:54
- Collision Model2:45
- Activation Energy5:11
- Arrhenius Proposed9:54
- 2 Requirements for a Successful Reaction15:39
- Rate Constant17:53
- Arrhenius Equation19:51
- Example 125:00
- Activation Energy & the Values of K32:12
- Example 236:46

AP Practice for Kinetics

29m 8s

- Intro0:00
- Kinetics0:43
- Example 10:44
- Example 26:53
- Example 38:58
- Example 411:36
- Example 516:36
- Example 6: Part A21:00
- Example 6: Part B25:09

VI. Equilibrium

Equilibrium, Part 1

46m

- Intro0:00
- Equilibrium1:32
- Introduction to Equilibrium1:33
- Equilibrium Rules14:00
- Example 1: Part A16:46
- Example 1: Part B18:48
- Example 1: Part C22:13
- Example 1: Part D24:55
- Example 2: Part A27:46
- Example 2: Part B31:22
- Example 2: Part C33:00
- Reverse a Reaction36:04
- Example 337:24

Equilibrium, Part 2

40m 53s

- Intro0:00
- Equilibrium1:31
- Equilibriums Involving Gases1:32
- General Equation10:11
- Example 1: Question11:55
- Example 1: Answer13:43
- Example 2: Question19:08
- Example 2: Answer21:37
- Example 3: Question33:40
- Example 3: Answer35:24

Equilibrium: Reaction Quotient

45m 53s

- Intro0:00
- Equilibrium0:57
- Reaction Quotient0:58
- If Q > K5:37
- If Q < K6:52
- If Q = K7:45
- Example 1: Part A8:24
- Example 1: Part B13:11
- Example 2: Question20:04
- Example 2: Answer22:15
- Example 3: Question30:54
- Example 3: Answer32:52
- Steps in Solving Equilibrium Problems42:40

Equilibrium: Examples

31m 51s

- Intro0:00
- Equilibrium1:09
- Example 1: Question1:10
- Example 1: Answer4:15
- Example 2: Question13:04
- Example 2: Answer15:20
- Example 3: Question25:03
- Example 3: Answer26:32

Le Chatelier's principle & Equilibrium

40m 52s

- Intro0:00
- Le Chatelier1:05
- Le Chatelier Principle1:06
- Concentration: Add 'x'5:25
- Concentration: Subtract 'x'7:50
- Example 19:44
- Change in Pressure12:53
- Example 220:40
- Temperature: Exothermic and Endothermic24:33
- Example 329:55
- Example 435:30

VII. Acids & Bases

Acids and Bases

50m 11s

- Intro0:00
- Acids and Bases1:14
- Bronsted-Lowry Acid-Base Model1:28
- Reaction of an Acid with Water4:36
- Acid Dissociation10:51
- Acid Strength13:48
- Example 121:22
- Water as an Acid & a Base25:25
- Example 2: Part A32:30
- Example 2: Part B34:47
- Example 3: Part A35:58
- Example 3: Part B39:33
- pH Scale41:12
- Example 443:56

pH of Weak Acid Solutions

43m 52s

- Intro0:00
- pH of Weak Acid Solutions1:12
- pH of Weak Acid Solutions1:13
- Example 16:26
- Example 214:25
- Example 324:23
- Example 430:38

Percent Dissociation: Strong & Weak Bases

43m 4s

- Intro0:00
- Bases0:33
- Percent Dissociation: Strong & Weak Bases0:45
- Example 16:23
- Strong Base Dissociation11:24
- Example 213:02
- Weak Acid and General Reaction17:38
- Example: NaOH → Na⁺ + OH⁻20:30
- Strong Base and Weak Base23:49
- Example 424:54
- Example 533:51

Polyprotic Acids

35m 34s

- Intro0:00
- Polyprotic Acids1:04
- Acids Dissociation1:05
- Example 14:51
- Example 217:30
- Example 331:11

Salts and Their Acid-Base Properties

41m 14s

- Intro0:00
- Salts and Their Acid-Base Properties0:11
- Salts and Their Acid-Base Properties0:15
- Example 17:58
- Example 214:00
- Metal Ion and Acidic Solution22:00
- Example 328:35
- NH₄F → NH₄⁺ + F⁻34:05
- Example 438:03

Common Ion Effect & Buffers

41m 58s

- Intro0:00
- Common Ion Effect & Buffers1:16
- Covalent Oxides Produce Acidic Solutions in Water1:36
- Ionic Oxides Produce Basic Solutions in Water4:15
- Practice Example 16:10
- Practice Example 29:00
- Definition12:27
- Example 1: Part A16:49
- Example 1: Part B19:54
- Buffer Solution25:10
- Example of Some Buffers: HF and NaF30:02
- Example of Some Buffers: Acetic Acid & Potassium Acetate31:34
- Example of Some Buffers: CH₃NH₂ & CH₃NH₃Cl33:54
- Example 2: Buffer Solution36:36

Buffer

32m 24s

- Intro0:00
- Buffers1:20
- Buffer Solution1:21
- Adding Base5:03
- Adding Acid7:14
- Example 1: Question9:48
- Example 1: Recall12:08
- Example 1: Major Species Upon Addition of NaOH16:10
- Example 1: Equilibrium, ICE Chart, and Final Calculation24:33
- Example 1: Comparison29:19

Buffers, Part II

40m 6s

- Intro0:00
- Buffers1:27
- Example 1: Question1:32
- Example 1: ICE Chart3:15
- Example 1: Major Species Upon Addition of OH⁻, But Before Rxn7:23
- Example 1: Equilibrium, ICE Chart, and Final Calculation12:51
- Summary17:21
- Another Look at Buffering & the Henderson-Hasselbalch equation19:00
- Example 227:08
- Example 332:01

Buffers, Part III

38m 43s

- Intro0:00
- Buffers0:25
- Buffer Capacity Part 10:26
- Example 14:10
- Buffer Capacity Part 219:29
- Example 225:12
- Example 332:02

Titrations: Strong Acid and Strong Base

42m 42s

- Intro0:00
- Titrations: Strong Acid and Strong Base1:11
- Definition of Titration1:12
- Sample Problem3:33
- Definition of Titration Curve or pH Curve9:46
- Scenario 1: Strong Acid- Strong Base Titration11:00
- Question11:01
- Part 1: No NaOH is Added14:00
- Part 2: 10.0 mL of NaOH is Added15:50
- Part 3: Another 10.0 mL of NaOH & 20.0 mL of NaOH are Added22:19
- Part 4: 50.0 mL of NaOH is Added26:46
- Part 5: 100.0 mL (Total) of NaOH is Added27:26
- Part 6: 150.0 mL (Total) of NaOH is Added32:06
- Part 7: 200.0 mL of NaOH is Added35:07
- Titrations Curve for Strong Acid and Strong Base35:43

Titrations: Weak Acid and Strong Base

42m 3s

- Intro0:00
- Titrations: Weak Acid and Strong Base0:43
- Question0:44
- Part 1: No NaOH is Added1:54
- Part 2: 10.0 mL of NaOH is Added5:17
- Part 3: 25.0 mL of NaOH is Added14:01
- Part 4: 40.0 mL of NaOH is Added21:55
- Part 5: 50.0 mL (Total) of NaOH is Added22:25
- Part 6: 60.0 mL (Total) of NaOH is Added31:36
- Part 7: 75.0 mL (Total) of NaOH is Added35:44
- Titration Curve36:09

Titration Examples & Acid-Base Indicators

52m 3s

- Intro0:00
- Examples and Indicators0:25
- Example 1: Question0:26
- Example 1: Solution2:03
- Example 2: Question12:33
- Example 2: Solution14:52
- Example 3: Question23:45
- Example 3: Solution25:09
- Acid/Base Indicator Overview34:45
- Acid/Base Indicator Example37:40
- Acid/Base Indicator General Result47:11
- Choosing Acid/Base Indicator49:12

VIII. Solubility

Solubility Equilibria

36m 25s

- Intro0:00
- Solubility Equilibria0:48
- Solubility Equilibria Overview0:49
- Solubility Product Constant4:24
- Definition of Solubility9:10
- Definition of Solubility Product11:28
- Example 114:09
- Example 220:19
- Example 327:30
- Relative Solubilities31:04

Solubility Equilibria, Part II

42m 6s

- Intro0:00
- Solubility Equilibria0:46
- Common Ion Effect0:47
- Example 13:14
- pH & Solubility13:00
- Example of pH & Solubility15:25
- Example 223:06
- Precipitation & Definition of the Ion Product26:48
- If Q > Ksp29:31
- If Q < Ksp30:27
- Example 332:58

Solubility Equilibria, Part III

43m 9s

- Intro0:00
- Solubility Equilibria0:55
- Example 1: Question0:56
- Example 1: Step 1 - Check to See if Anything Precipitates2:52
- Example 1: Step 2 - Stoichiometry10:47
- Example 1: Step 3 - Equilibrium16:34
- Example 2: Selective Precipitation (Question)21:02
- Example 2: Solution23:41
- Classical Qualitative Analysis29:44
- Groups: 1-538:44

IX. Complex Ions

Complex Ion Equilibria

43m 38s

- Intro0:00
- Complex Ion Equilibria0:32
- Complex Ion0:34
- Ligan Examples1:51
- Ligand Definition3:12
- Coordination6:28
- Example 18:08
- Example 219:13

Complex Ions & Solubility

31m 30s

- Intro0:00
- Complex Ions and Solubility0:23
- Recall: Classical Qualitative Analysis0:24
- Example 16:10
- Example 216:16
- Dissolving a Water-Insoluble Ionic Compound: Method 123:38
- Dissolving a Water-Insoluble Ionic Compound: Method 228:13

X. Chemical Thermodynamics

Spontaneity, Entropy, & Free Energy, Part I

56m 28s

- Intro0:00
- Spontaneity, Entropy, Free Energy2:25
- Energy Overview2:26
- Equation: ∆E = q + w4:30
- State Function/ State Property8:35
- Equation: w = -P∆V12:00
- Enthalpy: H = E + PV14:50
- Enthalpy is a State Property17:33
- Exothermic and Endothermic Reactions19:20
- First Law of Thermodynamic22:28
- Entropy25:48
- Spontaneous Process33:53
- Second Law of Thermodynamic36:51
- More on Entropy42:23
- Example43:55

Spontaneity, Entropy, & Free Energy, Part II

39m 55s

- Intro0:00
- Spontaneity, Entropy, Free Energy1:30
- ∆S of Universe = ∆S of System + ∆S of Surrounding1:31
- Convention3:32
- Examining a System5:36
- Thermodynamic Property: Sign of ∆S16:52
- Thermodynamic Property: Magnitude of ∆S18:45
- Deriving Equation: ∆S of Surrounding = -∆H / T20:25
- Example 125:51
- Free Energy Equations29:22

Spontaneity, Entropy, & Free Energy, Part III

30m 10s

- Intro0:00
- Spontaneity, Entropy, Free Energy0:11
- Example 12:38
- Key Concept of Example 114:06
- Example 215:56
- Units for ∆H, ∆G, and S20:56
- ∆S of Surrounding & ∆S of System22:00
- Reaction Example24:17
- Example 326:52

Spontaneity, Entropy, & Free Energy, Part IV

30m 7s

- Intro0:00
- Spontaneity, Entropy, Free Energy0:29
- Standard Free Energy of Formation0:58
- Example 14:34
- Reaction Under Non-standard Conditions13:23
- Example 216:26
- ∆G = Negative22:12
- ∆G = 024:38
- Diagram Example of ∆G26:43

Spontaneity, Entropy, & Free Energy, Part V

44m 56s

- Intro0:00
- Spontaneity, Entropy, Free Energy0:56
- Equations: ∆G of Reaction, ∆G°, and K0:57
- Example 1: Question6:50
- Example 1: Part A9:49
- Example 1: Part B15:28
- Example 217:33
- Example 323:31
- lnK = (- ∆H° ÷ R) ( 1 ÷ T) + ( ∆S° ÷ R)31:36
- Maximum Work35:57

XI. Electrochemistry

Oxidation-Reduction & Balancing

39m 23s

- Intro0:00
- Oxidation-Reduction and Balancing2:06
- Definition of Electrochemistry2:07
- Oxidation and Reduction Review3:05
- Example 1: Assigning Oxidation State10:15
- Example 2: Is the Following a Redox Reaction?18:06
- Example 3: Step 1 - Write the Oxidation & Reduction Half Reactions22:46
- Example 3: Step 2 - Balance the Reaction26:44
- Example 3: Step 3 - Multiply30:11
- Example 3: Step 4 - Add32:07
- Example 3: Step 5 - Check33:29

Galvanic Cells

43m 9s

- Intro0:00
- Galvanic Cells0:39
- Example 1: Balance the Following Under Basic Conditions0:40
- Example 1: Steps to Balance Reaction Under Basic Conditions3:25
- Example 1: Solution5:23
- Example 2: Balance the Following Reaction13:56
- Galvanic Cells18:15
- Example 3: Galvanic Cells28:19
- Example 4: Galvanic Cells35:12

Cell Potential

48m 41s

- Intro0:00
- Cell Potential2:08
- Definition of Cell Potential2:17
- Symbol and Unit5:50
- Standard Reduction Potential10:16
- Example Figure 113:08
- Example Figure 219:00
- All Reduction Potentials are Written as Reduction23:10
- Cell Potential: Important Fact 126:49
- Cell Potential: Important Fact 227:32
- Cell Potential: Important Fact 328:54
- Cell Potential: Important Fact 430:05
- Example Problem 132:29
- Example Problem 238:38

Potential, Work, & Free Energy

41m 23s

- Intro0:00
- Potential, Work, Free Energy0:42
- Descriptions of Galvanic Cell0:43
- Line Notation5:33
- Example 16:26
- Example 211:15
- Example 315:18
- Equation: Volt22:20
- Equations: Cell Potential, Work, and Charge28:30
- Maximum Cell Potential is Related to the Free Energy of the Cell Reaction35:09
- Example 437:42

Cell Potential & Concentration

34m 19s

- Intro0:00
- Cell Potential & Concentration0:29
- Example 1: Question0:30
- Example 1: Nernst Equation4:43
- Example 1: Solution7:01
- Cell Potential & Concentration11:27
- Example 216:38
- Manipulating the Nernst Equation25:15
- Example 328:43

Electrolysis

33m 21s

- Intro0:00
- Electrolysis3:16
- Electrolysis: Part 13:17
- Electrolysis: Part 25:25
- Galvanic Cell Example7:13
- Nickel Cadmium Battery12:18
- Ampere16:00
- Example 120:47
- Example 225:47

XII. Light

Light

44m 45s

- Intro0:00
- Light2:14
- Introduction to Light2:15
- Frequency, Speed, and Wavelength of Waves3:58
- Units and Equations7:37
- Electromagnetic Spectrum12:13
- Example 1: Calculate the Frequency17:41
- E = hν21:30
- Example 2: Increment of Energy25:12
- Photon Energy of Light28:56
- Wave and Particle31:46
- Example 3: Wavelength of an Electron34:46

XIII. Quantum Mechanics

Quantum Mechanics & Electron Orbitals

54m

- Intro0:00
- Quantum Mechanics & Electron Orbitals0:51
- Quantum Mechanics & Electron Orbitals Overview0:52
- Electron Orbital and Energy Levels for the Hydrogen Atom8:47
- Example 113:41
- Quantum Mechanics: Schrodinger Equation19:19
- Quantum Numbers Overview31:10
- Principal Quantum Numbers33:28
- Angular Momentum Numbers34:55
- Magnetic Quantum Numbers36:35
- Spin Quantum Numbers37:46
- Primary Level, Sublevels, and Sub-Sub-Levels39:42
- Example42:17
- Orbital & Quantum Numbers49:32

Electron Configurations & Diagrams

34m 4s

- Intro0:00
- Electron Configurations & Diagrams1:08
- Electronic Structure of Ground State Atom1:09
- Order of Electron Filling3:50
- Electron Configurations & Diagrams: H8:41
- Electron Configurations & Diagrams: He9:12
- Electron Configurations & Diagrams: Li9:47
- Electron Configurations & Diagrams: Be11:17
- Electron Configurations & Diagrams: B12:05
- Electron Configurations & Diagrams: C13:03
- Electron Configurations & Diagrams: N14:55
- Electron Configurations & Diagrams: O15:24
- Electron Configurations & Diagrams: F16:25
- Electron Configurations & Diagrams: Ne17:00
- Electron Configurations & Diagrams: S18:08
- Electron Configurations & Diagrams: Fe20:08
- Introduction to Valence Electrons23:04
- Valence Electrons of Oxygen23:44
- Valence Electrons of Iron24:02
- Valence Electrons of Arsenic24:30
- Valence Electrons: Exceptions25:36
- The Periodic Table27:52

XIV. Intermolecular Forces

Vapor Pressure & Changes of State

52m 43s

- Intro0:00
- Vapor Pressure and Changes of State2:26
- Intermolecular Forces Overview2:27
- Hydrogen Bonding5:23
- Heat of Vaporization9:58
- Vapor Pressure: Definition and Example11:04
- Vapor Pressures is Mostly a Function of Intermolecular Forces17:41
- Vapor Pressure Increases with Temperature20:52
- Vapor Pressure vs. Temperature: Graph and Equation22:55
- Clausius-Clapeyron Equation31:55
- Example 132:13
- Heating Curve35:40
- Heat of Fusion41:31
- Example 243:45

Phase Diagrams & Solutions

31m 17s

- Intro0:00
- Phase Diagrams and Solutions0:22
- Definition of a Phase Diagram0:50
- Phase Diagram Part 1: H₂O1:54
- Phase Diagram Part 2: CO₂9:59
- Solutions: Solute & Solvent16:12
- Ways of Discussing Solution Composition: Mass Percent or Weight Percent18:46
- Ways of Discussing Solution Composition: Molarity20:07
- Ways of Discussing Solution Composition: Mole Fraction20:48
- Ways of Discussing Solution Composition: Molality21:41
- Example 1: Question22:06
- Example 1: Mass Percent24:32
- Example 1: Molarity25:53
- Example 1: Mole Fraction28:09
- Example 1: Molality29:36

Vapor Pressure of Solutions

37m 23s

- Intro0:00
- Vapor Pressure of Solutions2:07
- Vapor Pressure & Raoult's Law2:08
- Example 15:21
- When Ionic Compounds Dissolve10:51
- Example 212:38
- Non-Ideal Solutions17:42
- Negative Deviation24:23
- Positive Deviation29:19
- Example 331:40

Colligatives Properties

34m 11s

- Intro0:00
- Colligative Properties1:07
- Boiling Point Elevation1:08
- Example 1: Question5:19
- Example 1: Solution6:52
- Freezing Point Depression12:01
- Example 2: Question14:46
- Example 2: Solution16:34
- Osmotic Pressure20:20
- Example 3: Question28:00
- Example 3: Solution30:16

XV. Bonding

Bonding & Lewis Structure

48m 39s

- Intro0:00
- Bonding & Lewis Structure2:23
- Covalent Bond2:24
- Single Bond, Double Bond, and Triple Bond4:11
- Bond Length & Intermolecular Distance5:51
- Definition of Electronegativity8:42
- Bond Polarity11:48
- Bond Energy20:04
- Example 124:31
- Definition of Lewis Structure31:54
- Steps in Forming a Lewis Structure33:26
- Lewis Structure Example: H₂36:53
- Lewis Structure Example: CH₄37:33
- Lewis Structure Example: NO⁺38:43
- Lewis Structure Example: PCl₅41:12
- Lewis Structure Example: ICl₄⁻43:05
- Lewis Structure Example: BeCl₂45:07

Resonance & Formal Charge

36m 59s

- Intro0:00
- Resonance and Formal Charge0:09
- Resonance Structures of NO₃⁻0:25
- Resonance Structures of NO₂⁻12:28
- Resonance Structures of HCO₂⁻16:28
- Formal Charge19:40
- Formal Charge Example: SO₄²⁻21:32
- Formal Charge Example: CO₂31:33
- Formal Charge Example: HCN32:44
- Formal Charge Example: CN⁻33:34
- Formal Charge Example: 0₃34:43

Shapes of Molecules

41m 21s

- Intro0:00
- Shapes of Molecules0:35
- VSEPR0:36
- Steps in Determining Shapes of Molecules6:18
- Linear11:38
- Trigonal Planar11:55
- Tetrahedral12:45
- Trigonal Bipyramidal13:23
- Octahedral14:29
- Table: Shapes of Molecules15:40
- Example: CO₂21:11
- Example: NO₃⁻24:01
- Example: H₂O27:00
- Example: NH₃29:48
- Example: PCl₃⁻32:18
- Example: IF₄⁺34:38
- Example: KrF₄37:57

Hybrid Orbitals

40m 17s

- Intro0:00
- Hybrid Orbitals0:13
- Introduction to Hybrid Orbitals0:14
- Electron Orbitals for CH₄5:02
- sp³ Hybridization10:52
- Example: sp³ Hybridization12:06
- sp² Hybridization14:21
- Example: sp² Hybridization16:11
- σ Bond19:10
- π Bond20:07
- sp Hybridization & Example22:00
- dsp³ Hybridization & Example27:36
- d²sp³ Hybridization & Example30:36
- Example: Predict the Hybridization and Describe the Molecular Geometry of CO32:31
- Example: Predict the Hybridization and Describe the Molecular Geometry of BF₄⁻35:17
- Example: Predict the Hybridization and Describe the Molecular Geometry of XeF₂37:09

XVI. AP Practice Exam

AP Practice Exam: Multiple Choice, Part I

52m 34s

- Intro0:00
- Multiple Choice1:21
- Multiple Choice 11:22
- Multiple Choice 22:23
- Multiple Choice 33:38
- Multiple Choice 44:34
- Multiple Choice 55:16
- Multiple Choice 65:41
- Multiple Choice 76:20
- Multiple Choice 87:03
- Multiple Choice 97:31
- Multiple Choice 109:03
- Multiple Choice 1111:52
- Multiple Choice 1213:16
- Multiple Choice 1313:56
- Multiple Choice 1414:52
- Multiple Choice 1515:43
- Multiple Choice 1616:20
- Multiple Choice 1716:55
- Multiple Choice 1817:22
- Multiple Choice 1918:59
- Multiple Choice 2020:24
- Multiple Choice 2122:20
- Multiple Choice 2223:29
- Multiple Choice 2324:30
- Multiple Choice 2425:24
- Multiple Choice 2526:21
- Multiple Choice 2629:06
- Multiple Choice 2730:42
- Multiple Choice 2833:28
- Multiple Choice 2934:38
- Multiple Choice 3035:37
- Multiple Choice 3137:31
- Multiple Choice 3238:28
- Multiple Choice 3339:50
- Multiple Choice 3442:57
- Multiple Choice 3544:18
- Multiple Choice 3645:52
- Multiple Choice 3748:02
- Multiple Choice 3849:25
- Multiple Choice 3949:43
- Multiple Choice 4050:16
- Multiple Choice 4150:49

AP Practice Exam: Multiple Choice, Part II

32m 15s

- Intro0:00
- Multiple Choice0:12
- Multiple Choice 420:13
- Multiple Choice 430:33
- Multiple Choice 441:16
- Multiple Choice 452:36
- Multiple Choice 465:22
- Multiple Choice 476:35
- Multiple Choice 488:02
- Multiple Choice 4910:05
- Multiple Choice 5010:26
- Multiple Choice 5111:07
- Multiple Choice 5212:01
- Multiple Choice 5312:55
- Multiple Choice 5416:12
- Multiple Choice 5518:11
- Multiple Choice 5619:45
- Multiple Choice 5720:15
- Multiple Choice 5823:28
- Multiple Choice 5924:27
- Multiple Choice 6026:45
- Multiple Choice 6129:15

AP Practice Exam: Multiple Choice, Part III

32m 50s

- Intro0:00
- Multiple Choice0:16
- Multiple Choice 620:17
- Multiple Choice 631:57
- Multiple Choice 646:16
- Multiple Choice 658:05
- Multiple Choice 669:18
- Multiple Choice 6710:38
- Multiple Choice 6812:51
- Multiple Choice 6914:32
- Multiple Choice 7017:35
- Multiple Choice 7122:44
- Multiple Choice 7224:27
- Multiple Choice 7327:46
- Multiple Choice 7429:39
- Multiple Choice 7530:23

AP Practice Exam: Free response Part I

47m 22s

- Intro0:00
- Free Response0:15
- Free Response 1: Part A0:16
- Free Response 1: Part B4:15
- Free Response 1: Part C5:47
- Free Response 1: Part D9:20
- Free Response 1: Part E. i10:58
- Free Response 1: Part E. ii16:45
- Free Response 1: Part E. iii26:03
- Free Response 2: Part A. i31:01
- Free Response 2: Part A. ii33:38
- Free Response 2: Part A. iii35:20
- Free Response 2: Part B. i37:38
- Free Response 2: Part B. ii39:30
- Free Response 2: Part B. iii44:44

AP Practice Exam: Free Response Part II

43m 5s

- Intro0:00
- Free Response0:12
- Free Response 3: Part A0:13
- Free Response 3: Part B6:25
- Free Response 3: Part C. i11:33
- Free Response 3: Part C. ii12:02
- Free Response 3: Part D14:30
- Free Response 4: Part A21:03
- Free Response 4: Part B22:59
- Free Response 4: Part C24:33
- Free Response 4: Part D27:22
- Free Response 4: Part E28:43
- Free Response 4: Part F29:35
- Free Response 4: Part G30:15
- Free Response 4: Part H30:48
- Free Response 5: Diagram32:00
- Free Response 5: Part A34:14
- Free Response 5: Part B36:07
- Free Response 5: Part C37:45
- Free Response 5: Part D39:00
- Free Response 5: Part E40:26

AP Practice Exam: Free Response Part III

28m 36s

- Intro0:00
- Free Response0:43
- Free Response 6: Part A. i0:44
- Free Response 6: Part A. ii3:08
- Free Response 6: Part A. iii5:02
- Free Response 6: Part B. i7:11
- Free Response 6: Part B. ii9:40
- Free Response 7: Part A11:14
- Free Response 7: Part B13:45
- Free Response 7: Part C15:43
- Free Response 7: Part D16:54
- Free Response 8: Part A. i19:15
- Free Response 8: Part A. ii21:16
- Free Response 8: Part B. i23:51
- Free Response 8: Part B. ii25:07

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3 answers

Last reply by: Professor Hovasapian

Fri Dec 14, 2018 4:03 AM

Post by Nick Jiang on November 28 at 11:51:37 PM

Hi Professor,

I have a few questions.

1. Is Heat of combustion also the energy required to combust one mole of a substance at one atmosphere?

2. I know this is somewhat unrelated from this lecture, but why do network covalent solids generally(there are exceptions, right?) have higher melting points than ionic compounds?

3. I have a question about a problem in the SAT Chemistry Subject Test:

One mole of each of the following substances is dissolved in 1.0 kg of water. Which solution will have the lowest freezing point?

(A) NaC2H3O2

(B) NaCl

(C) MgCl2

(D) CH3OH

(E) C6H12O6

The reasoning I currently have is that the lowest freezing point means the weakest IMFs because it will take the least energy and temp to break the forces/bonds in the compounds. I'm alittle confused how to proceed here; I know that the answer should be between CH3OH and C6H12O6 because they are the only molecules there.

Another issue is that the solution says that MgCl2 is the answer because the most ions dissociate, but this would mean that the problem is asking for the compound with the strongest forces/bonds.

Thanks!

1 answer

Last reply by: Professor Hovasapian

Fri Jan 5, 2018 4:03 AM

Post by Matthew Stringer on January 5 at 12:24:47 AM

I probably should take my calculator off of scientific mode. I sat here for ten minutes redoing the same calculation for Example 1 until I realized I was getting it right the whole time. I just don't read. lol. Great lecture! Your course has been a huge help! You are about 1000% better than my Ap Chem teacher because rather than randomly giving us formulas, you give us explanations and also I actually understand what you're talking about. My current Ap chem teacher just gives us formulas without any context or explanation. She just tells us what numbers to plug in. She has these packets that aren't consistent with units. Thanks so much!

-Matthew

1 answer

Last reply by: Professor Hovasapian

Mon Feb 20, 2017 7:14 AM

Post by Woong ryeol Yoo on February 19, 2017

Hi, Professor. Hovasapian.

I'm very confused about a problem set from Princeton Review.

The problem set says that NH3 has a hydrogen bond.

I was very confused about this because I thought hydrogen bond was a bond formed between molecules. But, this problem set just gave me NH3 without any other molecules shown.

This is the exact question:

11. Which of the following lists of species is in order of increasing boiling points?

A. H2, N2, NH3

B. N2, NH3, H2

C. NH3, H2, N2

D. NH3, N2, H2

The anwser is A.

But, the answer key also just says that NH3 has hydrogen bond.

Can a hydrogen bond form within a molecule like this question says?

1 answer

Last reply by: Professor Hovasapian

Thu Dec 17, 2015 1:06 AM

Post by Jason Smith on December 12, 2015

Hi professor! Hope you're having a good day.

Is the following reasoning correct?

The reason why sodium chloride dissolves in water is because the ion-dipole forces between H2O and the Na cation/Cl anion are stronger than the hydrogen bonds between the H and O atoms?

Am I conceptualizing this correctly?

Thank you in advance!

1 answer

Last reply by: Professor Hovasapian

Tue Mar 17, 2015 4:22 PM

Post by Jason Smith on March 14, 2015

I have a theoretical question that I would love your opinion on professor: if you continue to heat a substance once it has reached a gaseous phase, what will happen? Is there such a thing as "infinitely hot"? Will the gas particles themselves "disappear"? Or will they simply move more quickly? Is there ever a point where the gas particles get so hot that they move infinitely quick? Hope these questions make sense.

1 answer

Last reply by: Professor Hovasapian

Tue Mar 17, 2015 4:10 PM

Post by Jason Smith on March 14, 2015

For the flask example at the 13:00 minute mark or so (when you talked about vapor pressure), is the top of the flask closed off to the surrounding environment (have a top on it to prevent vapor from escaping). Also, vapor will vapor pressure always remain constant assuming that the temperature remains the same? Thank you professor.

1 answer

Last reply by: Professor Hovasapian

Tue Jul 23, 2013 5:20 AM

Post by KyungYeop Kim on July 20, 2013

I have two questions on solutions.. In a simple equation MgCl2 >>> Mg + 2Cl, I seem to confuse about what 2Cl means. I do know it means that 1 mole MgCl2 produces 2 mole Cl, but what about concentration? If I'm asked to calculate concentration of Cl-, then would I be correct in finding out the concentration of MgCl2 and dividing it by 2?

Sometimes Cl exists in gas form. Does it hold true in above case? also, if there's Cl2 instead of 2Cl, does it make any difference in calculating concentration and etc.?

Solution is not a very intuitive concept for me.. Thank you in advance.

1 answer

Last reply by: Professor Hovasapian

Sun Jun 2, 2013 2:55 PM

Post by KyungYeop Kim on May 31, 2013

A Hydrogen atom is said to be partially charged, thus being attracted to other differently charged atoms of molecules. (For instance, the hydrogen bonds in between H2O molecules) But what's special about hydrogen bonding? Aren't all partially charged atoms attracted to the oppositely charged atoms? Or is it something that only happens to hydrogen?

0 answers

Post by Professor Hovasapian on April 20, 2013

Hi Antie,

R is the Ideal Gas Constant. For Gases, in units of L*atm/mol*K the value is 0.08206. In units of J/mol*K it is 8.31. Sice we are discussing energy, we use the 8.31value.

For an element or compound in a given state (solid, Liquid or gas), this equation expresses how much energy is gained or lost by that compound upon increase or decrease of Temperature, respectively. The origin is based on Heat Capacity: the amount of energy necessary to raise the temp of a compound 1degree Celsius (or Kelvin).

Now, heat of fusion is a simple conversion. The heat of Fusion is the amount of energy a compound gains or loses as it transitions from Solid to Liquid and Liquid to solid, respectively.

So, if something has a Heat of fusion of 10 kJ/mol, and there are 3 mols of it, then it requires 30 kJ of energy to melt it...or it releases 30 kJ into the surroundings when it freezes.

Let me know if this does not make sense. And no worries -- please feel free to ask as many questions as you would like and need. I'm happy to help in any way I can.

Take good care

Raffi

1 answer

Last reply by: Professor Hovasapian

Sun Apr 21, 2013 3:01 AM

Post by Antie Chen on April 19, 2013

In Clausius-Clapeyron Equation, what's the R represent? And how I know it is 8.3145 J/mol*K in Example 1?

I am also confused the origin of the equation q=m*c*delta T and the equation to calculate heat of fusion in Example 2?

Sorry for so much question :P