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

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)

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

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

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)

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

In this video we'll be going over E2 reactions. Timestamp: (0:00) - Intro (0:34) -Alpha/Beta Carbon/Hydrogen (1:14) - General E2 Reaction (2:10) - Factors affecting E2 Reactions (substrate) (2:44) - Factors affecting E2 Reactions (base) (2:52) - Factors affecting E2 Reactions (leaving group) (3:22) - Zaitzev's Rule (3:33) - Zaitzev's Product (3:50) - Hofmann Product (5:41) - Bulky Bases used in E2 Reactions (6:40) - E2 reactions with non-bulky bases (8:02) - E2 reactions with bulky bases (9:52) - Anti-periplanar (anti-coplanar) (10:42) - Syn-periplanar (syn coplanar)

In this video, we'll be comparing SN1 and SN2 reactions. (0:00) Intro (0:49) -Definition (Nucleophile, Electrophile, Leaving Group, Substrate) (1:13)- SN1 Rate Law 1:28- SN2 Rate Law (1:36)- SN1 two-part reaction (1:55) -SN2 concerted reaction (2:20) -SN1 nucleophile (2:43)- SN2 nucleophile (3:18)- SN1 substrate (3:51)- SN2 substrate (4:21)- SN1 solvent (4:34)- SN2 solvent (4:47)- SN1/SN2 leaving group (5:40)- SN1 stereochemistry (6:04)- SN2 stereochemistry (6:22)- SN1 rearrangement (6:43)- SN2 rearrangement Check out the visual aspect here on our YouTube: https://youtu.be/4XlJZokd5Dc Music from Tunetank.com danyvin - Pretty Lofi (Copyright Free Music) Download free: https://tunetank.com/t/1ugo/3741-pretty-lofi

In this episode, we'll be going over SN1 reactions and factors affecting it. (0:00) - Intro (0:24) -Definitions (Nucleophile, Electrophile, Leaving Group, Substrate) (0:40) - General SN1 reaction (1:05) -SN1 reaction - Headless Horseman Reaction (2:08)- Strength of Nucleophile (2:27)- Steric Effects of Electrophile (3:03)- Solvent 3:16- Leaving Group (3:42)- Hydride Shift (5:22)- Methyl Shift (5:48)- Stereochemistry (6:20)- SN1 Summary Sheet Check out the visual portion of this episode on our youtube: https://youtu.be/cr7salBKHPw

In this episode, we'll be going over SN2 reactions and the factors affecting it. (0:00)- Intro (0:22)- Definitions (Nucleophile, Electrophile, Leaving Group, Substrate) (0:40)- General SN2 reaction (2:24)- SN2 Reaction- The Great Rear Ended Car Crash (3:06)- SN2 and strength of nucleophile (3:58)- Steric effects of electrophile (4:55)- Solvents 6:03- Leaving Group (7:14)- Stereochemistry (8:24)- SN2 Summary Sheet Check out the visual aspect of this video on our youtube. https://youtu.be/tOgInZX4Xgo

In this episode, we'll be going over functional groups seen in organic chemistry. (0:00) - Intro (0:13)- Defining a functional group (0:23)- Hydrocarbons (1:34)- Functional Groups with Oxygen (3:02)- Carboxylic Acid Derivatives (3:16)- Functional Groups with Nitrogen Check out the visual portion here on our youtube: https://youtu.be/F-u_UD4xYSs