Learning With Levi: Recent Episodes
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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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)
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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
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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
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https://youtu.be/cr7salBKHPw
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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
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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
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