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Organic Chemistry II Videos
Price: $20/mo
Subject: Videos
Instructor: David Tompkins
Overview:
Recorded lectures and videos for all subjects within the Organic II Curriculum by David Tompkins.
Videos Included:
1. Resonance
2. Acid-Base: An Organic Perspective
3. Acid-Base: Application
4. 1H NMR: Chemical Shift
5. 1H NMR: Topicity & Equivalence
6. 1H NMR: Chemical Equivalence
7. 1H NMR: Integration
8. 1H NMR: Splitting
9. 1H NMR: Solving Spectra: Techniques
10. 1H NMR: Structural Elucidation I
11. 1H NMR: Structural Elucidation II
12. 1H NMR: Structural Elucidation III
13. 1H NMR: Structural Elucidation IV
14. Alkyne Reactions: Intro
15. Alkynes: Addition of HX
16. Alkynes: Bridge Intermediates
17. Alkynes: Mercury-Catalyzed Hydration
18. Alkynes: Hydroboration-Oxidation
19. Alkynes: Reduction
20. Alkynes: Acetylide Ions
21. Alkynes: Synthesis
22. Dienes and Delocalization
23. Conjugated Dienes: MO’s, 1,2/1,4 Additions, and K vs.T
24. Diels-Alder
25. Aromaticity
26. Aromatic Compounds
27. Frost Diagrams
28. Aromaticity: Concepts
29. EAS: Intro
30. EAS: Halogenation
31. EAS: Friedel-Crafts Alkylation
32. EAS: Friedel-Crafts Acylation
33. EAS: Nitration and Sulfonation
34. EAS: Directing Groups & EDG's
35. EAS: EWG's as Deactivators
36. EAS: Activators and Deactivators
37. EAS: Regioselectivity
38. NBS: Allylic & Benzylic Bromination & Synthesis
39. Alkyl, Allyl, Vinyl, Aryl, and Benzyl Reactivities
40. Allylic & Benzylic Reactivity towards SN1
41. Allylic, Benzylic, and Phenolic Acidity
42. Allylic & Benzylic Carbanions
43. Allylic & Benzylic Reactivity towards SN2
44. Aryl & Vinyl Halides: Inert Towards SN1/SN2
45. Nucleophilic Aromatic Substitution: Addition-Elimination
46. Nucleophilic Aromatic Substitution: Elimination-Addition via Benzyne
47. Substitution Mechanisms: Aryl, Vinyl, Alkyl, Allylic & Benzylic Halides
48. Alcohol Oxidation
49. Organometallics I
50. Organometallics II
51. Intro to Carbonyls
52. Aldehydes & Ketones: Reactivity
53. Aldehydes & Ketones: Irreversible Additions
54. Aldehydes & Ketones: Reduction
55. Aldehydes & Ketones: Cyanohydrin Formation & Reversal
56. Aldehydes & Ketones: Hydration
57. Carbonyl Reactivity
58. Aldehydes & Ketones: Addition of Oxygen Nucleophiles
59. Aldehydes & Ketones: Acetals & Ketals
60. Aldehydes & Ketones: Protecting Groups
61. Aldehydes & Ketones: Synthesis
62. Aldehydes & Ketones: Imines & Enamines
63. Condensation Reactions of Aldehydes & Ketones
64. Aldehydes & Ketones: Wittig Reaction
65. Intramolecular Wittig Olefination
66. Alpha-Beta Unsaturated Ketones: 1,2 (Direct) vs. 1,4 (Conjugate) Addition
67. Carboxylic Acid Derivatives 1: Intro to Nucleophilic Acyl Substitution
68. Carboxylic Acid Derivatives 2: Relative Reactivity
69. Trends in Carbonyl Reactivity, α-H acidity, and Carbonyl O Basicity
70. Trends in Carbonyl Reactivity
71. Carboxylic Acid Derivatives 3: Acidity and Hydrolysis
72. Acetal Formation & Fischer Esterification
73. Carboxylic Acid Derivatives 4: Synthesis and Stoichiometry
74. Carboxylic Acid Derivatives 5: Irreversible Additions and Reductions
75. Acid Chlorides & Organocuprates (Gilman Reagents)
76. Carbonyl Reactivity: Reduction with Hydrides
77. Synthesis via Carbonyls
78. Enolates 1: Intro, Tautomerization, and Halogenation
79. Enolates 2: Alkylation
80. Enolates 3: Named Reactions
81. Enolates 4: Aldol Reactions
82. Aldol Reactions: Crossed, Intramolecular, and Retro
83. Enolates 5: Claisen Condensations
84. Claisen and Dieckmann Condensations I
85. Claisen and Dieckmann Condensations II
86. Enolates 6: Michael Addition and Robinson Annulation
87. Michael, Robinson, and Retrosynthesis
88. Enolate Retrosynthesis
89. Decarboxylation and Synthesis
90. Alpha-Carbon Nucleophiles
91. Basicity of Nitrogen-Containing Compounds
92. Amine Basicity
93. Amine Synthesis via SN2
94. Reductive Amination
95. Reduction of Amides & Nitriles
96. Hoffman Elimination
97. Curtius Rearrangement
98. Amine Synthesis
99. Amino Acids: pI and Chirality
100. Amino Acid Synthesis
101. Carbohydrates: Acyclic Stereochemistry
102. Carbohydrates: Epimerization
103. Carbohydrates: Tautomerization
104. Carbohydrates: D-Glucose
105. Carbohydrates: Cyclization
106. Carbohydrates: Cyclic D vs. L
107. Carbohydrates: The Anomeric Carbon
108. Carbohydrates: Mutarotation
109. Carbohydrates: Glycosides
110. Carbohydrates: Anomeric Carbon Reactivity
111. Carbohydrates: Reducing Sugars
112. Carbohydrates: Glycosidic Linkages
113. Carbohydrates: Review
114. Themes 1: Carbonyl Stability
115. Themes 2: Resonance Predicts Reactivity
116. Themes 3: Acid-Base: Kinetics vs. Thermodynamics
Preview
Testimonials
"David was practically the only reason I got an A in organic chemistry. He was on time, prepared, and always went above and beyond to teach me concepts and make sure I was prepared for exams. Couldn’t have done it without him!"
"I highly recommend David for organic chemistry tutoring. He is extremely knowledgeable and great at explaining both the essential foundations and tricky, higher-level concepts."
"Coming up with hundreds of exam-like questions on the spot, David has challenged me to think critically and comprehensively about chemistry. He has helped me to believe in myself and has instilled a sense of confidence in my ability to excel in chemistry that I didn't have before knowing him. Never being condescending, David will answer all of your questions, going above and beyond what any professor ever will."
“David tailored every moment of our sessions to fit my needs and supplied me with countless practice problems and explanations. He patiently clarified concepts and taught me strategies that helped me reason through and solve complex problems.”
“David can actually teach - not just answer questions like most tutors. You can come to him with a topic you are struggling with and he will run with it, coming up with problems on the fly and making sure you truly understand the material. He took me from a student who got a 50 on my first orgo exam to an A- student.”
"Working with David has completely changed how I view the subject of Chemistry. A class like Orgo once intimidated me, but having him in my corner gave me the skills and confidence to conquer the course."
