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Predicting Products of Organic Reactions: E2 Elimination and Substitution
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Leaving Group Conversions - Using HX
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02:03
Why do we need to convert Alcohol into a good leaving group?
Johnny Betancourt
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02:16
Using HX acids via SN2 reaction.
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3354
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29
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07:20
Using HX acids via SN1 reaction.
Johnny Betancourt
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Leaving Group Conversions - Sulfonyl Chlorides
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05:33
Learning the mechanism of Sulfonyl Chlorides.
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The SN2 Mechanism
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Ranking reactivity toward SN2
Johnny Betancourt
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7
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08:33
Drawing the SN2 Mechanism
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131
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28
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11:57
Understanding the properties of SN2.
Johnny Betancourt
7164
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79
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20
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SN1 Reaction
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10:49
Drawing the SN1 Mechanism
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49
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01:13
Why highly substituted leaving groups favor SN1.
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5515
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8
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08:16
Understanding the properties of SN1.
Johnny Betancourt
5722
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71
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14
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E2 Mechanism
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04:42
Understanding the properties of E2.
Johnny Betancourt
5441
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61
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8
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09:36
Drawing the E2 Mechanism.
Johnny Betancourt
7230
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109
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25
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02:03
Rank reactivity toward E2
Johnny Betancourt
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80
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8
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Acidity of Aromatic Hydrocarbons
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Aromatic hydrocarbon acidity
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24
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13
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02:41
Comparing hydrocarbon acidity
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2225
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22
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8
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01:50
Determining hydrocarbon acitidy
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1911
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16
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pKa Values
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07:45
Identifying pKa values
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12
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09:36
The 12 pKa values you want to memorize (because they are important!).
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Resonance Structures
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03:24
How to draw a resonance hybrid.
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03:34
The rules you need for resonance:
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01:32
How to determine which structure is most stable.
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더 많은 영상 (7)
Chirality
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Drawing Mirror Images and Determining Chirality
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05:10
What is chirality?
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03:44
Drawing Mirror Images and Determining Chirality
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Cahn-Ingold-Prelog Nomenclature
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R and S Naming- Step 4
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Why stereoisomers need their own naming system.
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01:19
Determining Priorities
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