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College Chemistries and Physics
Preparation
01
02
03
04-ISOMERS-AND-STEREOCHEMISTRY
05-ALKENES
06-ALKYNES
07-CONJUGATION
08-SUBSTITUTION-REACTIONS
09-ELIMINATION-REACTIONS
10-RADICAL-REACTIONS
11-MASS-SPECTROMETRY
12-IR-SPECTROSCOPY
13-NMR-SPECTROSCOPY
14-ALCOHOLS-ETHERS-AND-EPOXIDES
15-AROMATIC-COMPOUNDS
16-KETONES-AND-ALDEHYDES
17-CARBOXYLIC-ACIDS-AND-CARBOXYLIC-ACID-DERIVATIVES
18-ALPHA-ADDITIONS
19-AMINES
20-CARBON-CARBON-COUPLING-REACTIONS
2012 College Organic Chemistry
$35.00
21:51:39
01
$15.00
1:54:05
21:50
01.1 Molecular Structures and Bonding
17:15
01.2 Resonance
34:07
01.3 Acids and Bases
40:53
01.4 Nomenclature
02
$10.00
47:51
18:56
02.1 Intermolecular Forces
10:56
02.2 Newman Projections
17:59
02.3 Cycloalkanes
03
$10.00
14:37
5:60
03.1 Intro to Arrow Pushing
8:37
03.2 Rxn Coordinate Diagrams
04-ISOMERS-AND-STEREOCHEMISTRY
$15.00
1:13:13
19:07
04.1 ISOMERS and STEREOCHEMISTRY Vocabulary
16:23
04.2 Assigning R and S
24:54
04.3 Isomers with Multiple Chiral Centers, Diastereomers, Meso Compounds
3:56
04.4 Amine Inversion
8:53
04.5 Chiral Compounds with No Chiral Centers
05-ALKENES
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1:38:26
6:04
05.01 ALKENES Nomenclature
16:04
05.02 Alkene Rxns Intro to Electrophilic Addition
10:48
05.03 Addition of HBr, HCl and HI
6:57
05.04 Acid Catalyzed Hydration
8:25
05.05 Acid Catalyzed Addition of an Alcohol with Rearrangement
13:31
05.06 Addition of Br2, Br2 with H2O, and Br2 with Alcohol
6:13
05.07 Oxymercuration Demurcuration and Alkoxymercuration Demurcuration
6:39
05.08 Hydroboration Oxidation
2:26
05.09 Catalytic Hydrogenation
4:57
05.10 Addition of HBr with Peroxide (ROOR)
4:05
05.11 Epoxidation and Trans Hydroxylation
0:59
05.12 Syn Hydroxylation
5:49
05.13 Carbene Additions
2:34
05.14 Ozonolysis of Alkenes
2:55
05.15 Stability of Alkenes and Heats of Hydrogenation
06-ALKYNES
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44:45
10:10
06.01 ALKYNES Structure, Nomenclature and Acidity
3:19
06.02 Synthesis of Alkynes
7:39
06.03 Acetylene Zipper Rxn
4:28
06.04 Reduction of Alkynes
1:18
06.05 Addition of HBr, HCl and HI
0:45
06.06 Addition of HBr with Peroxide (ROOR)
1:13
06.07 Addition of Br2
6:54
06.08 Acid Catalyzed Hydration and Hydroboration Oxidation
4:22
06.09 Rxns of Acetylide Ions
4:37
06.10 Synthesis Problems with Alkynes
07-CONJUGATION
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1:26:00
37:58
07.1 CONJUGATION Conjugated Systems and Pi Molecular Orbitals
14:56
07.2 Addition Rxns to Conjugated Systems Kinetic vs Thermodynamic Products
33:06
07.3 Diels Alder Rxns
08-SUBSTITUTION-REACTIONS
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58:09
58:09
08.1 SUBSTITUTION RXNS SN1 and SN2 Rxns
09-ELIMINATION-REACTIONS
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47:57
28:55
09.1 ELIMINATION RXNS E1 and E2 Rxns
13:14
09.2 Distinguishing Between SN1, SN2, E1 and E2 Rxns
5:48
09.3 Pinacol Rearrangement
10-RADICAL-REACTIONS
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29:21
18:22
10.1 RADICAL RXNS Halogenation with Br2 light and Cl2 light
4:31
10.2 Bromination with NBS
6:28
10.3 Addition of HBr ROOR to an Alkene
11-MASS-SPECTROMETRY
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54:15
37:12
11.1 MASS SPECTROMETRY Predicting Fragmentation Patterns
17:03
11.2 Interpreting Mass Spectra
12-IR-SPECTROSCOPY
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30:06
10:48
12.1 IR SPECTROSCOPY IR Theory
19:18
12.2 Interpreting IR Spectra
13-NMR-SPECTROSCOPY
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1:30:15
10:18
13.1 NMR SPECTROSCOPY NMR Theory
12:10
13.2 C13 NMR
13:45
13.3 H NMR Determining the Number of Signals
22:02
13.4 H NMR Splitting and Multiplicity
17:33
13.5 Determining an Unknown from NMR Spectra
14:27
13.6 Determining an Unknown from All the Spectra
14-ALCOHOLS-ETHERS-AND-EPOXIDES
1:27:52
8:35
14.01 ALCOHOLS ETHERS AND EPOXIDES Nomenclature of Alcohols
14:52
14.02 Acidity of Alcohols
4:03
14.03 Reaction of Alcohols with HCl HBr and HI
15:04
14.04 Reaction of Alcohols with PBr3 SOCl2 and TsCl
10:02
14.05 Dehydration of Alcohols with H2SO4
4:59
14.06 Oxidation of Alcohols with Chromic Acid and PCC
5:45
14.07 Reduction of Ketones Aldehydes and Esters to form Alcohols
16:43
14.08 Nomenclature Synthesis and Reactions of Ethers
7:49
14.09 Ring Opening of Epoxides
15-AROMATIC-COMPOUNDS
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1:56:04
6:45
15.01 AROMATIC COMPOUNDS Nomenclature
29:05
15.02 Aromaticity
8:38
15.03 Intro to EAS Rxns
5:18
15.04 EAS Nitration
3:02
15.05 EAS Sulfonation
3:07
15.06 EAS Chlorination and Bromination
3:12
15.07 EAS Friedel Crafts Alkylation
5:03
15.08 EAS Friedel Crafts Acylation
1:06:54
15.09 EAS Not So Common Acylations with Anhydrides and Carboxylic Acids
1:51
15.10 EAS Formylation Gattermann Koch Rxn
14:14
15.11 EAS Activating and Deactivating GroupsOrtho Para and Meta Directors
11:45
15.12 EAS Rxns with Substituted Benzenes
1:36
15.13 Benzylic Oxidation with Permanganate
2:02
15.14 Clemmensen and Wolff Kishner Reductions
1:30
15.15 Nitro Reduction
4:28
15.16 Rxns of Arenediazonium Salts
8:04
15.17 Nucleophilic Aromatic Substitution NAS
5:18
15.18 EAS with Non benzenoid Aromatic Compounds
16-KETONES-AND-ALDEHYDES
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1:09:02
3:38
16.01 KETONES AND ALDEHYDES Nomenclature
10:06
16.02 Synthesis of Ketones and Aldehydes
3:42
16.03 Intro to Nucleophilic Addition
2:40
16.04 Nucleophilic Addition of Acetylides and Grignards
14:50
16.05 Hydride Reductions of Carbonyls
0:32
16.06 Reduction with H2
7:06
16.07 Addition of Amines Formation of Imines and Enamines
12:47
16.08 Addition f Water and Alcohols Formation of Hydrates, Ketals, and Acetals and Carbonyl Protection
7:26
16.09 1, 2 vs 1, 4 Addition to Conjugated Carbonyls
6:15
16.10 The Wittig Rxn
17-CARBOXYLIC-ACIDS-AND-CARBOXYLIC-ACID-DERIVATIVES
$15.00
1:20:24
18:23
17.1 CARBOXYLIC ACIDS AND CARBOXYLIC ACID DERIVATIVES Nomenclature
14:55
17.2 Properties and Synthesis of Carboxylic Acids
23:14
17.3 Summary of Nucleophilic Acyl Substitution Rxns
5:27
17.4 Examples of Nucleophilic Acyl Substitution
11:40
17.5 Mechanisms of Nucleophilic Acyl Substitution
6:45
17.6 Gabriel Synthesis
18-ALPHA-ADDITIONS
$15.00
1:52:15
12:52
18.01 ALPHA ADDITIONS Acidity of the Alpha Carbon
2:57
18.02 Intro to Alpha Additions
10:21
18.03 Alpha Haolgenation, the Iodoform Test, and the HVZ Reaction
7:40
18.04 Alpha Alkylation and the Stork Rxn
7:45
18.05 The Michael Rxn 1, 4 Addition
35:18
18.06 Aldol Condensation
7:45
18.07 Robinson Annulation
12:20
18.08 Claisen Condensation
4:45
18.09 Beta Decarboxylation
10:32
18.10 Malonic Ester and Acetoacetic Ester Syntheses
19-AMINES
$15.00
57:02
12:14
19.01-Nomenclature-and-Basicity
6:22
19.02-Gabriel-Synthesis
6:29
19.03-Reduction-of-Nitriles-Azides-Nitro-compounds-and-Amides
1:18
19.04-Hofmann-Rearrangement
3:00
19.05-Curtius-and-Schmidt-Syntheses
2:53
19.06-Beckman-Rearrangement
5:09
19.07-Hinsberg-Test
8:35
19.08-Hofmann-Elimination
2:08
19.09-Cope-Elimination
4:44
19.10-Phase-Transfer-Catalysis
4:10
19.11-Reductive-Amination
20-CARBON-CARBON-COUPLING-REACTIONS
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0:00
20.1-Carbon-Carbon-Coupling-Reactions
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