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Organic Chemistry Unit 1: Key Concepts, Vocabulary, and Skills Study Guide

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Atomic Structure

  • Three rules about orbitals you need to know.
    02:54
  • Understanding the hydrogen isotopes.
    03:06
  • The difference between atomic numbers and atomic mass.
    01:44

Atomic Structure

  • Three rules about orbitals you need to know.
    02:54
  • Understanding the hydrogen isotopes.
    03:06
  • The difference between atomic numbers and atomic mass.
    01:44

Electronegativity

  • Differences between ionic, polar and covalent bonds
    11:33

Atomic Structure

  • Three rules about orbitals you need to know.
    02:54
  • Understanding the hydrogen isotopes.
    03:06
  • The difference between atomic numbers and atomic mass.
    01:44

Bonding Preferences

  • What is the difference between valence and octet electrons?
    02:04
  • Understanding the hydrogen isotopes.
    08:32
  • What is a valence electron?
    02:14

Sigma and Pi Bonds

  • Single bonds, double bonds, and triple bonds.
    06:00
  • Sigma bonds and pi bonds
    01:05
  • Sigma bonds and pi bonds
    00:59

Electronegativity

  • Differences between ionic, polar and covalent bonds
    11:33

Electronegativity

  • Differences between ionic, polar and covalent bonds
    11:33

Lewis Structure

  • Drawing the Lewis Structure for N2H4.
    04:12
  • How to use Organic Chemistry to make Lewis Structures easier.
    03:49

Octet Rule

  • LCAO model proves why Noble gases are so stable.
    03:48
  • The most important parts of the periodic table for organic chemistry
    02:24
  • How Noble gases are related to the octet rule.
    01:05

Formal Charges

  • Calculate the formal charges of ALL atoms.
    02:21
  • Calculating formal and net charge.
    01:34

Resonance Structures

  • How to draw a resonance hybrid.
    03:24
  • The rules you need for resonance:
    03:34
  • How to determine which structure is most stable.
    01:32

Constitutional Isomers

  • Isomeric Relationships
    03:28
  • Using the flowchart to determine isometric relationships.
    05:02
  • Isomeric Relationships
    02:56

Condensed Structural Formula

  • How to draw condensed mixed structures.
    05:21
  • How to interpret condensed structures.
    06:06

Hybridization

  • How carbon creates 4 partially-filled orbitals.
    02:53
  • Bond sites, hybridization, and intermediate orbitals
    04:58
  • Introduction to the reactive intermediates.
    02:47

Hybridization

  • How carbon creates 4 partially-filled orbitals.
    02:53
  • Bond sites, hybridization, and intermediate orbitals
    04:58
  • Introduction to the reactive intermediates.
    02:47

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

pKa Values

  • Identifying pKa values
    07:45
  • The 12 pKa values you want to memorize (because they are important!).
    09:36

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

pKa Values

  • Identifying pKa values
    07:45
  • The 12 pKa values you want to memorize (because they are important!).
    09:36

Cis vs Trans

  • Why we need to use the E/Z naming system
    02:07
  • What does E and Z stand for?
    00:50
  • How to name different types of double bonds or rings
    04:28

Conformational Isomers

  • Understanding what a conformer is.
    03:29

Reaction Mechanism

  • How to tell if charged molecules will react as nucleophiles or electrophiles.
    02:39
  • Nucleophile or Electrophile
    01:49
  • How to tell if uncharged molecules will react as nucleophiles or electrophiles.
    02:48

Types of Stereoisomers

  • Determine total number of stereoisomers
    00:49
  • How to predict the total number of stereoisomers.
    01:03
  • Draw stereoisomers and determine relationship
    07:41

Axial vs Equatorial

  • What is a chair conformation?
    01:05
  • How chairs flip from one conformation to another
    02:22
  • How chairs flip from one conformation to another
    04:26

Chirality Test 2 - Stereocenters

  • Determining Chirality using Stereocenter
    02:25
  • Determining Chirality using Stereocenter
    00:36
  • The difference between chiral and trigonal centers.
    02:38

Ring Strain

  • Understanding Heat of Combustion
    01:11
  • What is torsional strain?
    02:00
  • Lowest Heat of Combustion
    02:34

Barrier To Rotation

  • 4 Values You Should Memorize
    02:54
  • Determining energy cost of eclipsed interaction
    03:00

Cis vs Trans

  • Why we need to use the E/Z naming system
    02:07
  • What does E and Z stand for?
    00:50
  • How to name different types of double bonds or rings
    04:28

Bonding Preferences

  • What is the difference between valence and octet electrons?
    02:04
  • Understanding the hydrogen isotopes.
    08:32
  • What is a valence electron?
    02:14

Intermolecular Forces

  • How dipole-dipole forces work.
    01:46
  • How IMFs are related to melting and boiling points.
    03:08
  • How Van der Waals forces work.
    03:01

Intermolecular Forces

  • How dipole-dipole forces work.
    01:46
  • How IMFs are related to melting and boiling points.
    03:08
  • How Van der Waals forces work.
    03:01

Resonance Structures

  • How to draw a resonance hybrid.
    03:24
  • The rules you need for resonance:
    03:34
  • How to determine which structure is most stable.
    01:32

Conjugation Chemistry

  • Conjugated states
    03:27
  • Definition of Conjugation
    05:29
  • Review of Common Resonance Structures
    04:50

Fischer Projection

  • Introduction to different projections.
    01:15
  • How to convert Fischer projections into bondline structures
    05:45
  • Convert the following Fischer projection into bondline structure.
    03:38

Monosaccharides - Haworth Projections

  • Monosaccharides - Haworth Projections
    04:03

Enantiomeric Excess

  • Calculating Enantiomeric Excess and Observed Rotation
    00:50
  • How to calculate enantiomeric excess.
    04:21
  • Calculating Enantiomeric Excess and Observed Rotation
    03:59

Enantiomeric Excess

  • Calculating Enantiomeric Excess and Observed Rotation
    00:50
  • How to calculate enantiomeric excess.
    04:21
  • Calculating Enantiomeric Excess and Observed Rotation
    03:59

Chirality Test 1 - Internal Line of Symmetry

  • Determining Chirality with Plane of Symmetry
    00:25
  • Determining Chirality with Plane of Symmetry
    01:10
  • How and when to use the internal line of symmetry test.
    01:25

Naming Bicyclic Compounds

  • How to name a bridged bicyclic
    04:39
  • The two types of bicyclic molecules
    01:55
  • How to name a fused bicyclic
    03:27

Reaction Mechanism

  • How to tell if charged molecules will react as nucleophiles or electrophiles.
    02:39
  • Nucleophile or Electrophile
    01:49
  • How to tell if uncharged molecules will react as nucleophiles or electrophiles.
    02:48

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

Acid and Base Definitions

  • Lewis vs. Bronsted-Lowry Definition
    07:46
  • The Bronsted-Lowry definition of acids and bases.
    00:54
  • Equilibrium constant and conjugates.
    02:11

Functional Groups

  • Assigning Degrees to Alkyl Halides
    01:30
  • Why we need functional groups.
    01:49
  • The difference between aldehydes and ketones.
    03:08

Solubility

  • Introducing common solvents and other molecules in organic chemistry.
    02:01
  • Understanding “like dissolves like”.
    01:47

Alkane Nomenclature

  • Naming the root chain
    01:02
  • Provide the IUPAC name for the following alkane
    07:08
  • The different parts of an IUPAC name
    03:43

Skeletal Structure

  • How bondline is different from Lewis Structures.
    04:03
  • Conversion of ethanol from electron dot to bondline
    01:50

Chirality

  • Drawing Mirror Images and Determining Chirality
    03:24
  • What is chirality?
    05:10
  • Drawing Mirror Images and Determining Chirality
    03:44

Chirality Test 1 - Internal Line of Symmetry

  • Determining Chirality with Plane of Symmetry
    00:25
  • Determining Chirality with Plane of Symmetry
    01:10
  • How and when to use the internal line of symmetry test.
    01:25

Chirality Test 2 - Stereocenters

  • Determining Chirality using Stereocenter
    02:25
  • Determining Chirality using Stereocenter
    00:36
  • The difference between chiral and trigonal centers.
    02:38

Cahn-Ingold-Prelog Nomenclature

  • R and S Naming- Step 4
    03:07
  • Why stereoisomers need their own naming system.
    01:48
  • Determining Priorities
    01:19

Optical Activity

  • Specific rotation vs. observed rotation.
    05:43

Enantiomeric Excess

  • Calculating Enantiomeric Excess and Observed Rotation
    00:50
  • How to calculate enantiomeric excess.
    04:21
  • Calculating Enantiomeric Excess and Observed Rotation
    03:59