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Clutch Prep = Textbook specific videos to help you pass your toughest science classes.

1. Alcohol Nomenclature
2. Ether Nomenclature
3. Epoxide Nomenclature
4. Thiol and Sulfide Nomenclature
5. Synthesis of Alcohols
6. Leaving Group Conversions HX
7. Leaving Group Conversions SOCl2 and PBr3
8. Leaving Group Conversions Sulfonate Esters
9. Leaving Group Conversions Conversion Summary
10. Ether Synthesis Reaction 1
11. Cleavage of Ethers
12. Alcohol Protecting Groups: t- Butyl Ether Protecting Groups
13. Alcohol Protecting Groups: Silyl Ether Protecting Groups
14. Epoxide Ring Opening 2
15. Reactions of Thiols
16. Oxidation of Sulfides
17. Oxidation Example 1
18. Oxidation Jones Reagent Mechanism
19. Preparation of Organometallics: General Reaction
20. Preparation of Organometallics Ruining Organometallics
21. Reactions of Organometallics
22. Carbonyl Protecting Groups
23. Synthetic Cheatsheet
24. Moving Functionality
25. Alkynide Alkylation
26. Alkane Halogenation
27. Purpose of Analytical Techniques
28. IR Spect General Features
29. IR Spect Frequencies
30. IR Spect Drawing: Spectra Hydrocarbons
31. IR Spect Drawing Spectra: Alcohols and Amines
32. 1H NMR General Features
33. 1H NMR Number of Signals: General Assumption
34. 1H NMR Number of Signals: Example 1
35. 1H NMR Chemical Shifts
36. 1H NMR Spin Splitting: Splitting without J values
37. 1H NMR Spin Splitting: Example 1
38. Building Molecular Sentences
39. Definition of Conjugation
40. Review of Common Resonance Structures
41. Stability of Conjugated Intermediates
42. Allylic Halogentation: General Mechanism
43. Conjugated Hydrohalogenation General Mechanism
44. Kinetic vs Thermodynamic Control
45. Diels Alder Reaction General Features
46. Introduction to Aromaticity
47. Four Tests of Aromaticity
48. Counting Pi Electrons
49. Aromaticity of Hydrocarbons
50. 6annulene vs 8annulene
51. Aromaticity of Heterocycles
52. Inscribed Polygon Method
53. Benzene Nomenclature
54. Acidity of Aromatic Hydrocarbons
55. Basicity of Aromatic Heterocycles: Do all lone pairs react equally
56. Resonance of Fulvalenes
57. EAS Introduction Conceptual Review
58. EAS Reactions
59. EAS Halogenation
60. EAS Nitration
61. Reduction of Nitro Groups
62. Activity and Directing Effects
63. EAS Ortho vs Para Positions
64. Protection of Aniline Derivatives
65. Limitations of Friedel Crafts Alkyation
66. Blocking Groups Sulfonic Acid
67. Mechanism
68. EAS Proposing Aromatic Synthesis
69. Diazo Replacement Reactions
70. Diazo Sequence Groups
71. Diazo Proposing Aromatic Synthesis
72. SNAr Mechanism: General Mechanism
73. Benzyne Pathway: General Mechanism
74. Donating vs Withdrawing Groups
75. O,P positions vs Meta Positions
76. Aldehyde Nomenclature
77. Ketone Nomenclature
78. Intro to Redox
79. Oxidation Reagents
80. Ozonolysis
81. Reduction Reagents
82. Why LiAlH4 doesn't work
83. LiAl(ot-Bu)3H on Acid Chlorides
84. Alkyne Hydration
85. Nucleophilic Addition
86. Addition of Cyanide
87. Nitrile Hydrolysis
88. Organometallics on Ketones
89. Overview of Nucleophilic Addition of Solvents
90. Hydrates Mechanism
91. Hemiacetals General Features
92. Acetals as Protecting Groups
93. Thioacetals and Raney Nickel Reduction
94. Imines and Enamines: General Reactions
95. Imines and Enamines: Mechanism
96. Addition of Amine Derivatives
97. Wolff Kischner Reduction General Reaction
98. Ketones from Acid Chloride
99. Ketones from Nitriles General Reaction
100. Box Out Method and Full Mechanism
101. Intro to Carboxylic Acid Derivatives
102. Carboxylic Acids
103. Ester Nomenclature
104. Nitrile Nomenclature
105. Anhydride Nomenclature
106. Amide Nomenclature
107. Synthesis of Acid Chlorides
108. Fischer Esterification (Simplified): General Reaction
109. Fischer Esterification: General Reaction
110. Acid Catalyzed Ester Hydrolysis: General Reaction
111. Base Catalyzed Ester Hydrolysis (Saponification)
112. Base Catalyzed Transesterification: General Reaction
113. Lactones and Lactams
114. Carbonation of Grignard Reagents
115. Decarboxylation: General Mechanism
116. Unusual Acidity of the Alpha Carbon
117. Tautomers of Dicarbonyl Compounds
118. Formation of Enolates
119. Acid vs Base Catalyzed
120. Overview of Alpha Alkylations and Acylations
121. Enolate Alkylation and Acylation: General Reaction
122. Enamine Alkylation and Acylation
123. Beta-Dicarbonyl Synthesis Pathway
124. Acetoacetic Ester Synthesis: General Reactions
125. Malonic Ester Synthesis: General Reactions
126. Condensation Reactions
127. Aldol Condensation
128. Directed Condensations
129. Claisen Schmidt Reaction
130. Claisen Condensation
131. Diketones
132. General Reaction
133. Robinson Annulation
134. Naming Primary Amines
135. Primary Amines as Substituents
136. Amine Alkylation: General Reaction
137. The Primary Amines Flowchart
138. Four Ways to Make a Primary Amine Precursor
139. Reductive Amination
140. Curtius Rearragement
141. Hofmann Rearragement: General Reaction
142. Cope Elimination General Reaction
143. Hofmann Elimination General Reaction

In this video tutorial series, study the second part of your first Organic Chemistry course while completing all the work on the provided worksheets. Clutch Prep offers textbook-specific videos to help you pass your toughest science classes.

Check out the list of Organic Chemistry textbooks they cover here: https://www.clutchprep.com/organic