Learning With Levi Learning With Levi

In this video, we’ll be going over the second part of the alkene addition reactions  

1️st part - https://open.spotify.com/episode/5FTNjDsqt6lvaJ5dPZZiz3?si=3fd8ff32b5e24b82 

Timestamp 

(0:00) - Intro 

(0:25) - Epoxidation Opening With Acid 

(1:17) - Halogenation of Alkenes 

(2:01) - Halohydrin Formation 

(3:00) - Hydrogen Halide  

(3:47)- Hydrogen Halide (rearrangement) 

(4:23)- Hydroboration of Alkenes 

(5:43)- Hydration by Oxymercuration-Demercuration  

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In this video we’ll be going over Markovnikov vs Anti-Markovnikov Rule and some addition reactions 

Timestamp  

(0:48) - Markovnikov Rule  

(1:46) - Anti-Markovnikov Rule  

(3:27) - Hydration of Alkenes  

(4:18) - Hydrogenation of Alkenes  

(5:04) - Dihydroxylation of Alkenes (Osminium Tetroxide)  

(5:58) - Dihydroxylation of Alkenes (Potassium Permanganate, Cold )  

(6:43) - Oxidative Cleavage (Potassium Permanganate, Warm)  

(7:33) - Oxidative Cleavage (Ozonolysis) 

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In this video we’ll be helping you decide which way a reaction will go with certain conditions (SN1, SN2, E1, and E2) 

Timestamp: 

(0:49) - Nucleophilicity and Basicity (rows) 

(1:13)  - Nucleophilicity and Columns  

(2:00) - Reagent acting as nucleophile only 

(2:25) - Reagent acting as a strong base only 

(2:44) -Reagent acting as strong base / strong nucleophile 

(3:20) -Reagent acting as weak base/ weak nucleophile 

(3:47) -Reagent acting as nucleophile only (primary or secondary substrate) 

(4:09) -Reagent acting as nucleophile only (tertiary substrate) 

(4:20) -Reagent acting as a strong base only (primary, secondary, or tertiary substrate) 

(4:39) -Reagent acting as strong base / strong nucleophile (primary substrate) 

(5:04) -Reagent acting as strong base / strong nucleophile (secondary substrate) 

(5:13) -Reagent acting as strong base / strong nucleophile (tertiary substrate) 

(5:28) -Reagent acting as weak base/ weak nucleophile (primary or secondary substrate) 

(5:36) -Reagent acting as weak base/ weak nucleophile (tertiary substrate) 

(6:00) -Regiochemistry/Stereochemistry for SN1 

(6:13) -Regiochemistry/Stereochemistry for SN2 

(6:22) -Regiochemistry/Stereochemistry for E1 

(6:29) -Regiochemistry/Stereochemistry for E2 



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In this video we’ll be comparing all the reactions (SN1, SN2, E1, and E2).

Timestamp: 

(0:00) - Intro 

(0:33) - Rate Law differences 

(1:12) - Base/Nucleophile differences 

(2:33) - Substrate differences 

(4:07) -Solvent differences 

(4:53) -Stereochemistry differences 

(6:02) -Rearrangement differences

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In this video we’ll be comparing E1 and E2 Reactions

Timestamp: 

(0:00) - Intro 

(0:31) - E1 Rate Law 

(0:49) - E2 Rate Law 

(0:58) - E1 two step reaction 

(1:20) - E2 concerted reaction 

(1:33) - E1 (base) 

(1:54) - E2 (base) 

(2:11) - E1 (substrate) 

(2:34) - E2 (Substrate) 

(2:46) - E1 (leaving group) 

(2:59) - E2 (leaving group) 

(3:12) - E1 (stereochemistry) 

(3:31) - E2 (stereochemistry) 

(3:57) - E1 (rearrangement) 

(4:12) -E2 (rearrangement)   

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 In this video we’ll be going over E1 reactions.  

(0:00) - Intro 

(1:41) - E1 Reaction - Stuck With Debt Reaction 

(2:20) - Zaitsev's Rule 

(3:27) -Rearrangement in E1 Reaction

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