Chem 51b Topic Index

Topic Name Video Lecture URL
Course Info https://www.youtube.com/watch?v

Alkyl Halides and Elimination Reactions https://www.youtube.com/watch?v
Nucleophilic Substitution: Review https://www.youtube.com/watch?v
Elimination Reactions https://www.youtube.com/watch?v
Alkenes: Structure and Stability https://www.youtube.com/watch?v
Relative Stabilities of Alkenes https://www.youtube.com/watch?v
The Mechanisms of Elimination https://www.youtube
The Effect of the Base https://www.youtube.com/watch?v
Solvent Effects https://www.youtube.com/watch?v
Leaving Group Effects https://www.youtube.com/watch?v
Structure of the Substrate https://www.youtube.com/watch?v
Regioselectivity of the E2 Reaction: The Zaitsev Rule https://www.youtube.com/watch?v
Regioselectivity of the E2 Reaction: The Zaitsev Rule https://www.youtube.com/watch?v
The Stereochemistry of the E2 Reaction https://www.youtube.com/watch?v
The Stereochemistry of the E2 Reaction https://www.youtube.com/watch?v
Competition between Sn2 vs E2 https://www.youtube.com/watch?v
Rate Law and Mechanism of the E1 Reaction https://www.youtube.com/watch?v
Alkene model https://www.youtube.com/watch?v
Rate Law and Mechanism of the E1 Reaction https://www.youtube.com/watch?v
Energy Diagram for an E1 Reaction https://www.youtube.com/watch?v
Important points on E1 Reaction https://www.youtube.com/watch?v
Examples of E1 Reactions https://www.youtube.com/watch?v
Competition between SN1 and E1 https://www.youtube.com/watch?v
Kinetic Isotope Effect https://www.youtube.com/watch?v
Double Elimination https://www.youtube.com/watch?v
Elimination Reaction Handout https://www.youtube.com/watch?v
Animations https://www.youtube.com/watch?v
Introduction https://www.youtube.com/watch?v
Nomenclature of Alcohols https://www.youtube.com/watch?v
Nomenclature of Ethers https://www.youtube.com/watch?v
Preparation of Alcohols, Ethers, Epoxides https://www.youtube.com/watch?v
Elimination Reactions of Alcohols: Dehydration https://www.youtube.com/watch?v
Elimination Reactions of Alcohols: Dehydration https://www.youtube.com/watch?v
Carbocation Rearrangement https://www.youtube.com/watch?v
Conversion of Alcohols to Alkyl Halides with H-X https://www.youtube.com/watch?v
Secondary and Tertiary Alkyl Halides https://www.youtube.com/watch?v
Other Methods for Converting Alcohols into Alkyl Halides https://www.youtube.com/watch?v
Converting Alcohols into Sulfonate Esters https://www.youtube.com/watch?v
Converting Alcohols into Sulfonate Esters https://www.youtube.com/watch?v
Substitution Reactions of Ethers https://www.youtube.com/watch?v
Reactions of Epoxides: Acid-Catalyzed Ring Opening https://www.youtube.com/watch?v
Nucleophilic Ring Opening https://www.youtube.com/watch?v
Nucleophilic Ring Opening https://www.youtube.com/watch?v
Alternative to Dehydration of Primary Alcohols https://www.youtube.com/watch?v
Alkenes: Introduction https://www.youtube.com/watch?v
Molecular Formula and Degree of Unsaturation https://www.youtube.com/watch?v
Nomenclature of Alkenes https://www.youtube.com/watch?v
Reactions of Alkenes: Electrophilic Addition https://www.youtube.com/watch?v
Addition of Hydrogen Halides to Alkenes https://www.youtube.com/watch?v
Transition State https://www.youtube.com/watch?fe
Carbocation Intermediate https://www.youtube.com/watch?fe
Stereochemistry of Electrophilic Addition of HX https://www.youtube.com/watch?fe
Addition of Water to Alkenes https://www.youtube.com/watch?fe
Addition of Bromine and Chlorine to Alkenes https://www.youtube.com/watch?fe
Addition of Bromine and Chlorine to Alkenes https://www.youtube.com/watch?li
How is the enantiomer formed? https://www.youtube.com/watch?li
Important points about halogenation reaction https://www.youtube.com/watch?li
Regiochemistry in this addition https://www.youtub
Addition of Borane: Hydroboration/Oxidation https://www.youtube.com/watch?li
Addition of Borane: Hydroboration/Oxidation https://www.youtube.com/watch?li
Stereoselevtivity in Hydroboration Reactions https://www.youtube.com/watch?li
Reactions and Synthesis https://www.youtube.com/watch?li
Alkynes: Introduction https://www.youtube.com/watch?li
Nomenclature https://www.youtube.com/watch?li
Acidity of 1-Alkynes https://www.youtube.com/watch?li
Sample Flashcards https://www.youtube.com/watch?li
Acidity and s Character https://www.youtube.com/watch?li
Relative Acidities https://www.youtube.com/watch?li
Some Reactions after deprotonation https://www.youtube.com/watch?li
Preparation of Alkynes https://www.youtube.com/watch?li
Addition of Hydrogen Halides to Alkynes https://www.youtube.com/watch?v
Addition of Water to Alkynes: Hydration https://www.youtube.com/watch?v
Mechanism of Hydration https://www.youtube.com/watch?li
Important points about Hydration https://www.youtube.com/watch?li
Addition of Bromine and Chlorine to Alkynes https://www.youtube.com/watch?li
Hydroboration/Oxidation of Alkynes https://www.youtube.com/watch?li
Designing Synthesis: Part 1 https://www.youtube.com/watch?fe
Introduction: Oxidation & Reduction https://www.youtube.com/watch?fe
Recognizing Oxidation and Reduction of Organic Compounds https://www.youtube.com/watch?fe
Reduction Reactions https://www.youtube.com/watch?fe
Addition of Hydrogen to Alkenes https://www.youtube.com/watch?fe
Addition of Hydrogen to Alkenes https://www.youtube.com/watch?fe
Hydrogenation of Other Double Bonds https://www.youtube.com/watch?fe
Reduction of Alkynes https://www.youtube.com/watch?fe
Lindlar's Catalyst https://www.youtube.com/watch?fe
The Reduction of Polar C-X sigma bonds https://www.youtube.com/watch?fe
Oxidation Reactions: Oxidizing agents https://www.youtube.com/watch?fe
Expoxidation https://www.youtube.com/watch?fe
Sharpless Asymmetric Epoxidation https://www.youtube.com/watch?fe
Dihydroxylation https://www.youtube.com/watch?fe
Asymmetric Epoxidation https://www.youtube.com/watch?fe
Oxidative Cleavage of Alkenes: Ozonolysis https://www.youtube.com/watch?fe
Oxidation of Alcohols: Oxidation with Chromic Acid https://www.youtube.com/watch?fe
Oxidation with Pyridinium Chlorochromate https://www.youtube.com/watch?fe
Green Chemistry https://www.youtube.com/watch?fe
Designing Syntheses: Part 2 https://www.youtube.com/watch?li
Radical Reactions: Introduction https://www.youtube.com/watch?li
General Features of Radical Reactions https://www.youtube.com/watch?li
Reaction of a Radical X with a C-H Bond https://www.youtube.com/watch?li
Reaction of a Radical X with a C=C Bond https://www.youtube.com/watch?li
Radical Mechanisms https://www.youtube.com/watch?li
Halogenation of Alkanes https://www.youtube.com/watch?li
Mechanism 1 https://www.youtube.com/watch?li
Mechanism 2 https://www.youtube.com/watch?li
Selectivity and Stability https://www.youtube.com/watch?li
Radical Substitution of Benzylic and Allylic Hydrogens https://www.youtube.com/watch?li
Radical Substitution of Benzylic and Allylic Hydrogens https://www.youtube.com/watch?li
Stereochemistry of Radical Reactions https://www.youtube.com/watch?li
Radical Addition of HBr to an Alkene https://www.youtube.com/watch?li
Radical Initiators https://www.youtube.com/watch?li
The Peroxide Effect https://www.youtube.com/watch?li
Autooxidation https://www.youtube.com/watch?li
Preventing Autooxidation: Addition of Antioxidants (Free-Radical Sc https://www.youtube.com/watch?li
Conjugation https://www.youtube.com/watch?li
Conjugation https://www.youtube.com/watch?fe
Conformations of Conjugated Dienes https://www.youtube.com/watch?fe
Electrophilic Addition Reactions of Isolated Dienes https://www.youtube.com/watch?fe
Electrophilic Addition Reactions of Conjugated Dienes: 1,2 and 1,4 Ahttps://www.youtube.com/watch?fe
Kinetic vs Thermodynamic Products https://www.youtube.com/watch?fe
The diels-alder Reactions https://www.youtube.com/watch?fe
The diels-alder Reactions https://www.youtube.com/watch?li
Characteristics of the Diels-Alder Reaction: Mechanism https://www.youtube.com/watch?li
Substituent Effects https://www.youtube.com/watch?li
Stereochemistry https://www.youtube.com/watch?li
The Diels-Alder Reaction is Stereospecific https://www.youtube.com/watch?li
The endo rule https://www.youtube.com/watch?li
The endo rule https://www.youtube.com/watch?li
Regioselectivity https://www.youtube.com/watch?li
Synthesis Using the Diels-Alder Reaction https://www.youtube.com/watch?li
The Structure of Benzene https://www.youtube.com/watch?li
Aromaticity https://www.youtube.com/watch?li
Molecular Orbital picture for Benzene https://www.youtube.com/watch?li
Molecular Orbital picture for Benzene https://www.youtube.com/watch?li
Some Chemical Consequences of Aromaticity https://www.youtube.com/watch?li
Nomenclature https://www.youtube.com/watch?li
Electrophilic Aromatic Substitution https://www.youtube.com/watch?li
Chlorination & Bromination of Benzene https://www.youtube.com/watch?li
Bromination of Benzene https://www.youtube.com/watch?v
Nitration of Benzene https://www.youtube.com/watch?v
Sulfonation of Benzene https://www.youtube.com/watch?v
Friedel-Crafts Alkylation https://www.youtube.com/watch?v
Friedel-Crafts Acylation https://www.youtube.com/watch?v
Substituent Effects in Electrophilic Aromatic Substitution https://www.youtube.com/watch?v
Ring Activating https://www.youtube.com/watch?v
Ring Deactivating https://www.youtube.com/watch?v
Ring Activating https://www.youtube.com/watch?fe
Ring Deactivating https://www.youtube.com/watch?fe
Effect of Sterics and More than One Substituent https://www.youtube.com/watch?fe
Methoxy, Hydroxy, and Amine Substituents https://www.youtube.com/watch?fe
Friedel-Crafts Alkylation & Acylation https://www.youtube.com/watch?fe
Nitration of Aniline Derivatives https://www.youtube.com/watch?fe
Reactions of Substituents on Benzene https://www.youtube.com/watch?fe
Reactions of Alkyl Substituents on Benzene https://www.youtube.com/watch?fe
Oxidation of Alkyl Groups Bonded to Aromatic Rings https://www.youtube.com/watch?fe
Reduction of Substituents Bonded to Benzene https://www.youtube.com/watch?fe
Clemmensen Reduction (HCl, Zn/Hg) https://www.youtube.com/watch?fe
Wolff-Kishner Reduction (H2NNH3, KOH) https://www.youtube.com/watch?fe
Nucleophilic Aromatic Substitution via Addition/Elimination https://www.youtube.com/watch?fe
Synthetic Applications of Electrophilic Aromatic Substitution https://www.youtube.com/watch?fe
Lecture Title Topic In-PoOut of ToPage Number in Lecture NoChemWiki Links
Lecture 01: Intr 0:03:27 0:14:34
Lecture 01: Intr 0:14:34 0:15:40 Ch. 8 pg 1
Lecture 01: Intr 0:15:40 0:30:59 Ch. 8 pg 1-3 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 01: Intr 0:30:59 0:34:54 Ch. 8 pg 3
Lecture 01: Intr 0:34:54 0:43:01 Ch. 8 pg 3-4 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 02: Alke 0:00:47 0:11:07 Ch. 8 pg 4-6 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 02: Alke 0:11:07 0:20:10 Ch. 8 pg 6-7
Lecture 02: Alke 0:20:10 0:21:02 Ch. 8 pg 8
Lecture 02: Alke 0:21:02 0:24:24 Ch. 8 pg 8
Lecture 02: Alke 0:24:24 0:25:19 Ch. 8 pg 8 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 02: Alke 0:25:19 0:33:35 Ch. 8 pg 8-9
Lecture 02: Alke 0:33:35 0:47:08 Ch. 8 pg 9-10 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 03: Ste 0:00:08 0:07:51 Ch. 8 pg 10
Lecture 03: Ste 0:07:51 0:43:22 Ch. 8 pg 11-13 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 04: Uni 0:00:11 0:08:23 Ch. 8 pg 13
Lecture 04: Uni 0:08:23 0:28:43 Ch. 8 pg 14-16 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 04: Uni 0:28:43 0:31:35 Ch. 8 pg 16 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 05: E1 0:01:12 0:04:19 Ch. 8 pg 16
Lecture 05: E1 0:04:19 0:06:13 Ch. 8 pg 16 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 05: E1 0:06:13 0:09:01 Ch. 8 pg 17
Lecture 05: E1 0:09:01 0:11:27 Ch. 8 pg 17
Lecture 05: E1 0:11:27 0:18:30 Ch. 8 pg 18
Lecture 05: E1 0:18:30 0:23:25 Ch. 8 pg 18-19
Lecture 05: E1 0:23:25 0:27:53 Ch. 8 pg 19
Lecture 05: E1 0:27:53 0:37:27 Ch. 8 pg 20
Lecture 05: E1 0:37:27 0:42:35 No Corresponding Page http://chemwiki.ucdavis.edu/Textbook_M
Lecture 05: E1 0:42:35 0:47:30 No Corresponding Page
Lecture 06: Alc 0:00:47 0:04:15 Ch. 9 pg 1
Lecture 06: Alc 0:04:15 0:10:47 Ch. 9 pg 2 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 06: Alc 0:10:47 0:14:59 Ch. 9 pg 2-3
Lecture 06: Alc 0:14:59 0:34:06 Ch. 9 pg 3-5 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 06: Alc 0:34:06 0:46:49 Ch. 9 pg 5-7 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 07: Conv 0:00:11 0:08:02 Ch. 9 pg 7-8
Lecture 07: Conv 0:08:02 0:24:12 Ch. 9 pg 8-10
Lecture 07: Conv 0:24:12 0:48:42 Ch. 9 pg 10-13 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 08: Met 0:00:49 0:03:33 Ch. 9 pg 13
Lecture 08: Met 0:03:33 0:31:28 Ch. 9 pg 14-16 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 08: Met 0:31:28 0:45:10 Ch. 9 pg 17-18 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 09: Rea 0:00:50 0:07:27 Ch. 9 pg 19
Lecture 09: Rea 0:07:27 0:19:07 Ch. 9 pg 20-21
Lecture 09: Rea 0:19:07 0:47:58 Ch. 9 pg 21-24 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 09: Rea 0:47:58 0:51:11 Ch. 9 pg 25
Lecture 10: Elec 0:00:17 0:14:32 Ch. 9 pg 25-27
Lecture 10: Elec 0:14:32 0:17:20 Ch. 9 pg 27 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 10: Elec 0:17:20 0:20:59 Ch. 10 Part 1 pg 1 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 10: Elec 0:22:39 0:26:08 Ch. 10 Part 2 pg 1
Lecture 10: Elec 0:26:08 0:40:27 Ch. 10 Part 2 pg 1-4 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 10: Elec 0:40:27 0:48:34 Ch. 10 Part 2 pg 4-5 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 11: Add 0:00:25 0:06:38 Ch. 10 Part 2 pg 5 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 11: Add 0:06:38 0:15:03 Ch. 10 Part 2 pg 5-6 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 11: Add 0:15:03 0:35:14 Ch. 10 Part 2 pg 6-9
Lecture 12: Add 0:00:09 0:07:43 Ch. 10 Part 2 pg 10 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 12: Add 0:07:43 0:13:11 Ch. 10 Part 2 pg 11
Lecture 13: Rea 0:01:12 0:08:52 Ch. 10 Part 2 pg 15-16 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 13: Rea 0:08:52 0:14:27 Ch. 10 Part 2 pg 16-17
Lecture 13: Rea 0:14:27 0:32:29 Ch. 10 Part 2 pg 17-18
Lecture 13: Rea 0:32:29 0:39:29 Ch. 11 pg 1 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 14: Elec 0:01:15 0:05:33 No Corresponding Page
Lecture 14: Elec 0:14:59 0:16:32 Ch. 11 pg 4
Lecture 14: Elec 0:30:54 0:41:59 Ch. 11 pg 6-7 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 14: Elec 0:41:59 0:50:06 Ch. 11 pg 8 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 15: Tau 0:00:54 0:07:13 Ch. 11 pg 8 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 15: Tau 0:07:13 0:12:03 Ch. 11 pg 9
Lecture 15: Tau 0:12:03 0:15:08 Ch. 11 pg 10
Lecture 15: Tau 0:15:08 0:28:59 Ch. 11 pg 10-12 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 15: Tau 0:28:59 0:37:10 Ch. 11 pg 12
Lecture 15: Tau 0:37:10 0:38:19 Ch. 12 pg 1
Lecture 15: Tau 0:38:19 0:47:20 Ch. 12 pg 1-2
Lecture 15: Tau 0:47:20 0:48:55 Ch. 12 pg 3
Lecture 15: Tau 0:48:55 0:50:26 Ch. 12 pg 3 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 16: Oxi 0:00:08 0:09:17 Ch. 12 pg 3-4 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 16: Oxi 0:09:17 0:12:29 Ch. 12 pg 4-5
Lecture 16: Oxi 0:12:29 0:17:44 Ch. 12 pg 5
Lecture 16: Oxi 0:17:44 0:20:10 Ch. 12 pg 6 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 16: Oxi 0:20:10 0:29:24 Ch. 12 pg 6
Lecture 16: Oxi 0:29:24 0:31:44 Ch. 12 pg 7
Lecture 16: Oxi 0:31:44 0:39:49 Ch. 12 pg 7-8 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 16: Oxi 0:39:49 0:43:50 Ch. 12 pg 8-9
Lecture 16: Oxi 0:43:50 0:50:23 Ch. 12 pg 9-10
Lecture 17: Gre 0:00:45 0:02:11 Ch. 12 pg 9-10
Lecture 17: Gre 0:02:11 0:09:13 Ch. 12 pg 10-11 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 17: Gre 0:09:13 0:20:10 Ch. 12 pg 11-12 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 17: Gre 0:20:10 0:24:49 Ch. 12 pg 13
Lecture 17: Gre 0:24:49 0:29:08 Ch. 12 pg 13-14
Lecture 17: Gre 0:29:08 0:40:04 Ch. 12 pg 14-16
Lecture 17: Gre 0:40:04 0:49:59 Ch. 15 pg 1-2
Lecture 18: Rad 0:01:30 0:01:54 Ch. 15 pg 2
Lecture 18: Rad 0:01:54 0:03:47 Ch. 15 pg 2
Lecture 18: Rad 0:03:47 0:04:58 Ch. 15 pg 3
Lecture 18: Rad 0:04:58 0:06:40 Ch. 15 pg 3
Lecture 18: Rad 0:06:40 0:09:16 Ch. 15 pg 3 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 18: Rad 0:09:16 0:27:05 Ch. 15 pg 4-5
Lecture 18: Rad 0:27:05 0:31:24 Ch. 15 pg 5
Lecture 18: Rad 0:31:24 0:43:52 Ch. 15 pg 6-7
Lecture 18: Rad 0:43:52 0:48:34 Ch. 15 pg 8 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 19: Ste 0:00:57 0:05:05 Ch. 15 pg 8-9 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 19: Ste 0:05:05 0:13:10 Ch. 15 pg 9
Lecture 19: Ste 0:13:10 0:24:57 Ch. 15 pg 10 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 19: Ste 0:24:57 0:26:12 Ch. 15 pg 11
Lecture 19: Ste 0:26:12 0:30:06 Ch. 15 pg 11
Lecture 19: Ste 0:30:06 0:37:46 Ch. 15 pg 12-13
Lecture 19: Ste 0:37:46 0:39:20 Ch. 15 pg 13
Lecture 19: Ste 0:39:20 0:51:01 Ch. 16 pg 1-2
Lecture 20: Con 0:02:39 0:03:29 Ch. 16 pg 2
Lecture 20: Con 0:03:29 0:16:27 Ch. 16 pg 2-3 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 20: Con 0:16:27 0:19:49 Ch. 16 pg 3
Lecture 20: Con 0:19:49 0:30:02 Ch. 16 pg 4 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 20: Con 0:30:02 0:42:12 Ch. 16 pg 5-6
Lecture 20: Con 0:42:12 0:50:29 Ch. 16 pg 7
Lecture 21: Diel 0:00:49 0:01:32 Ch. 16 pg 7 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 21: Diel 0:01:32 0:02:10 Ch. 16 pg 7
Lecture 21: Diel 0:09:37 0:18:41 Ch. 16 pg 9-10
Lecture 21: Diel 0:24:22 0:50:14 Ch. 16 pg 10-13
Lecture 22: Be 0:00:59 0:09:49 Ch. 16 pg 13 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 22: Be 0:09:49 0:15:01 Ch. 16 pg 14
Lecture 22: Be 0:15:01 0:24:27 Ch. 16 pg 14-15
Lecture 22: Be 0:24:27 0:30:11 Ch. 17 pg 1 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 22: Be 0:30:11 0:46:00 Ch. 17 pg 1-4 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 22: Be 0:46:00 0:50:45 Ch. 17 pg 5
Lecture 23: Elec 0:00:47 0:28:23 Ch. 17 pg 5-9 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 23: Elec 0:44:09 0:51:08 Ch. 18 pg 1-2 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 24: Aro 0:00:48 0:04:46 Ch. 18 pg 2-3
Lecture 24: Aro 0:04:46 0:10:46 Ch. 18 pg 3-4 http://chemwiki.ucdavis.edu/Organic_Che
Lecture 24: Aro 0:10:46 0:15:07 Ch. 18 pg 4
Lecture 24: Aro 0:15:07 0:32:06 Ch. 18 pg 5-6 http://chemwiki.ucdavis.edu/Wikitexts/Pu
Lecture 24: Aro 0:32:06 0:38:27 Ch. 18 pg 7 http://chemwiki.ucdavis.edu/Wikitexts/Pu
Lecture 24: Aro 0:38:27 0:41:14 Ch. 18 pg 8
Lecture 24: Aro 0:41:14 0:43:59 Ch. 18 pg 8
Lecture 24: Aro 0:43:59 0:50:36 Ch. 18 pg 8-9
Lecture 25: Subs 0:00:43 0:07:06 Ch. 18 pg 9
Lecture 25: Subs 0:07:06 0:15:57 Ch. 18 pg 10-11
Lecture 25: Subs 0:15:57 0:21:19 Ch. 18 pg 11-12 http://chemwiki.ucdavis.edu/Textbook_M
Lecture 25: Subs 0:42:19 0:47:40 Ch. 18 pg 15
Lecture 26: Synt 0:00:50 0:02:17 Ch. 18 pg 16
Lecture 26: Synt 0:02:17 0:04:36 Ch. 18 pg 16-17
Lecture 26: Synt 0:09:54 0:11:23 Ch. 18 pg 18 http://chemwiki.ucdavis.edu/?title=Organ
Lecture 26: Synt 0:11:23 0:14:23 Ch. 18 pg 18-19 http://chemwiki.ucdavis.edu/?title=Organ
Lecture 26: Synt 0:14:23 0:14:50 Ch. 18 pg 19 -21
Lecture 26: Synt 0:14:50 0:39:25 Ch. 18 pg 21-24
vis.edu/Organic_Chemistry/Organic_Chemistry_With_a_Biological_Emphasis/Chapter_08%3A_Nucleophilic_subst
vis.edu/Textbook_Maps/Organic_Chemistry_Textbook_Maps/Map%3A_Bruice_6ed_%22Organic_Chemistry%22/03
vis.edu/Organic_Chemistry/Reactions/Elimination_Reactions/Elimination_Reactions/C._Elimination_v._Substitutio
vis.edu/Textbook_Maps/Organic_Chemistry_Textbook_Maps/Map%3A_Bruice_2nd_%22Essential_Organic_Chemis
vis.edu/Organic_Chemistry/Hydrocarbons/Alkynes/Reactions_of_Alkynes/Hydroboration_Reactions_and_Oxidatio
vis.edu/Organic_Chemistry/Hydrocarbons/Alkenes/Reactions_of_Alkenes/Stereoselectivity_in_Addition_Reactions
vis.edu/Organic_Chemistry/Hydrocarbons/Alkynes/Reactions_of_Alkynes/Catalytic_Hydrogenation
vis.edu/Organic_Chemistry/Hydrocarbons/Alkenes/Reactions_of_Alkenes/Free_Radical_Reactions_of_Alkanes/Add
vis.edu/Organic_Chemistry/Conjugation/Conjugated_Dienes
vis.edu/Organic_Chemistry/Conjugation/Electrophilic_Attack_on_Conjugated_Dienes
vis.edu/Organic_Chemistry/UMM_chemwiki_project/Alkenes_and_alkynes/Diels-Alder_Cycloaddition
vis.edu/Organic_Chemistry/UMM_chemwiki_project/Alkenes_and_alkynes/Diels-Alder_Cycloaddition
vis.edu/Organic_Chemistry/Hydrocarbons/Aromatics/Properties_of_Benzene
vis.edu/Organic_Chemistry/UMM_chemwiki_project/Organic_Structure_and_Bonding/Aromaticity
vis.edu/Organic_Chemistry/UMM_chemwiki_project/Organic_Structure_and_Bonding/Aromaticity
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Nucleophilic Ring Opening https://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
Lecture 10: Electrophili 0:00:17
Alternative to Dehydration of https://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
Alkenes: Introduction https://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
Molecular Formula and Degreehttps://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
Nomenclature of Alkenes https://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
Reactions of Alkenes: Electrophhttps://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
Addition of Hydrogen Halides thttps://www.youtube.com/watch?v=mWcr38tWpAU&feature=player_de
0:14:32
0:17:20 http://chemwiki.ucdavis.edu/Textbook_Maps/Organic_Chemistry_Textbook_Maps/Map%3A_B
0:26:08
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modynamics_and_Kinetics/3.1%3A_Molecular_Formulas_and_the_Degree_of_Unsaturation
modynamics_and_Kinetics/3.2%3A_The_Nomenclature_of_Alkenes

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