Organic Chemistry
5.0
(1)
29 learners
What you'll learn
This course includes
- 11.5 hours of video
- Certificate of completion
- Access on mobile and TV
Course content
1 modules • 70 lessons • 11.5 hours of video
Organic Chemistry
70 lessons
• 11.5 hours
Organic Chemistry
70 lessons
• 11.5 hours
- Representing structures of organic molecules | Biology | Khan Academy07:29
- Naming simple alkanes | Organic chemistry | Khan Academy09:28
- Naming alkanes with alkyl groups | Organic chemistry | Khan Academy11:04
- Correction - 2-propylheptane should never be the name! | Organic chemistry | Khan Academy02:56
- Common and systematic naming: iso-, sec-, and tert- prefixes | Organic chemistry | Khan Academy13:32
- More Organic Chemistry Naming Examples 108:59
- Organic chemistry naming examples 2 | Organic chemistry | Khan Academy10:26
- Organic chemistry naming examples 3 | Organic chemistry | Khan Academy08:11
- Organic Chemistry Naming Examples 407:48
- Organic chemistry naming examples 4 | Organic chemistry | Khan Academy10:04
- Naming alkenes examples | Alkenes and Alkynes | Organic chemistry | Khan Academy08:27
- Naming alkyl halides | Substitution and elimination reactions | Organic chemistry | Khan Academy09:03
- sp3 hybridized orbitals and sigma bonds | Structure and bonding | Organic chemistry | Khan Academy16:23
- Pi bonds and sp2 hybridized orbitals | Structure and bonding | Organic chemistry | Khan Academy14:13
- Newman projections | Alkanes, cycloalkanes, and functional groups | Organic chemistry | Khan Academy14:22
- Newman projections 2 | Organic chemistry | Khan Academy11:12
- Chair and boat shapes for cyclohexane | Organic chemistry | Khan Academy12:29
- Double Newman diagram for methylcyclohexane | Organic chemistry | Khan Academy14:38
- Introduction to chirality | Stereochemistry | Organic chemistry | Khan Academy06:46
- Chiral examples 1 | Stereochemistry | Organic chemistry | Khan Academy11:02
- Chiral examples 2 | Stereochemistry | Organic chemistry | Khan Academy10:19
- Cahn-Ingold-Prelog system for naming enantiomers | Organic chemistry | Khan Academy11:02
- R,S (Cahn-Ingold-Prelog) naming system example 2 | Organic chemistry | Khan Academy11:08
- Stereoisomers, enantiomers, diastereomers, constitutional isomers and meso compounds | Khan Academy13:36
- cis-trans and E-Z naming scheme for alkenes | Alkenes and Alkynes | Organic chemistry | Khan Academy04:56
- Entgegen-Zusammen naming scheme for alkenes examples | Organic chemistry | Khan Academy06:04
- Introduction to reaction mechanisms | Alkenes and Alkynes | Organic chemistry | Khan Academy11:22
- Markovnikov's rule and carbocations | Alkenes and Alkynes | Organic chemistry | Khan Academy09:09
- Polymerization of alkenes with acid | Alkenes and Alkynes | Organic chemistry | Khan Academy12:04
- Sn2 Reactions11:31
- Sn2 Stereochemistry10:01
- Solvent Effects on Sn1 and Sn2 Reactions14:15
- Nucleophilicity (Nucleophile Strength)13:55
- Nucleophilicity vs. Basicity12:47
- E2 reactions | Substitution and elimination reactions | Organic chemistry | Khan Academy08:53
- E1 reactions | Substitution and elimination reactions | Organic chemistry | Khan Academy09:22
- Zaitsev's rule | Substitution and elimination reactions | Organic chemistry | Khan Academy13:29
- Comparing E2 E1 Sn2 Sn1 Reactions12:26
- E2 E1 Sn2 Sn1 Reactions Example 203:06
- E2 E1 Sn2 Sn1 Reactions Example 313:18
- Free radical reactions | Substitution and elimination reactions | Organic chemistry | Khan Academy13:45
- Alcohols | Alcohols, ethers, epoxides, sulfides | Organic chemistry | Khan Academy06:51
- Alcohol properties | Alcohols, ethers, epoxides, sulfides | Organic chemistry | Khan Academy09:24
- Resonance11:51
- Ether naming and introduction | Organic chemistry | Khan Academy10:59
- Cyclic ethers and epoxide naming | Organic chemistry | Khan Academy07:48
- Ring-opening Sn2 reaction of expoxides11:33
- Sn1 and Sn2 epoxide opening discussion07:58
- Aromatic Compounds and Huckel's Rule10:24
- Naming benzene derivatives introduction | Aromatic Compounds | Organic chemistry | Khan Academy08:40
- Electrophilic aromatic substitution | Aromatic Compounds | Organic chemistry | Khan Academy11:17
- Bromination of benzene | Aromatic Compounds | Organic chemistry | Khan Academy12:56
- Amine naming introduction | Amines | Organic chemistry | Khan Academy06:51
- Amine naming introduction | Amines | Organic chemistry | Khan Academy05:43
- Amine as Nucleophile in Sn2 Reaction14:45
- Amine in Sn2 part 210:22
- Sn1 Amine Reaction08:15
- Aldehyde introduction | Aldehydes and ketones | Organic chemistry | Khan Academy07:48
- Ketone naming | Aldehydes and ketones | Organic chemistry | Khan Academy08:44
- Friedel-Crafts acylation | Aromatic Compounds | Organic chemistry | Khan Academy11:18
- Friedel crafts acylation addendum | Aromatic Compounds | Organic chemistry | Khan Academy00:50
- Keto-enol tautomerization (by Sal) | Alpha Carbon Chemistry | Organic chemistry | Khan Academy08:03
- Carboxylic acid introduction | Carboxylic acids and derivatives | Organic chemistry | Khan Academy08:51
- Carboxylic acid naming | Carboxylic acids and derivatives | Organic chemistry | Khan Academy05:26
- Fischer esterification | Carboxylic acids and derivatives | Organic chemistry | Khan Academy17:12
- Acid chloride formation | Carboxylic acids and derivatives | Organic chemistry | Khan Academy11:49
- Amides, anhydrides, esters, and acyl chlorides | Organic chemistry | Khan Academy08:48
- Relative stability of amides, esters, anhydrides, and acyl chlorides | Khan Academy11:09
- Amide formation from acyl chloride | Carboxylic acids and derivatives | Khan Academy09:01
- Aldol reaction | Alpha Carbon Chemistry | Organic chemistry | Khan Academy11:41
