BrainChildren Chemistry
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Erland Stevens
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Erland Stevens - YouTube
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#7 plastic
a recap of different acetals and ketals
acetal protecting group: Erland Stevens
acetals and ketals as protecting groups
acetals and ketals: Erland Stevens
acid base ammonium
acid base compare
acid base intro
acid base mechanism
acid base pKa
acid base pKa table
acid base stabilization
acid deriv interconversions
acid derivatives and oxidation states
acid derivatives and the Jones oxidation
acid derivatives introduction
acid derivatives: amides
acid derivatives: esters
acid derivatives: example reactions
acid derivatives: hydride reagents
acid derivatives: hydrolysis
acid derivatives: nitriles
acid derivatives: organometallic reactions
acid derivatives: synthesis from CO2
acid-catalyzed reactions of acid derivatives
addition carbocation rearrangements
addition dihalogenation
addition epoxide opening with acid
addition epoxide opening with base
addition epoxide synthesis
addition halohydrin
addition hydration
addition hydroboration
addition hydroboration stereochemistry
addition hydrogenation
addition redox
addition stereochemistry
addition vicinal diols
additions hydrohalogenation
additions intro
alcohols E1
alcohols intro: Erland Stevens
alcohols leaving groups
alcohols SN1
alcohols SN2
alcohols tosylates
aldehyde-to-acetal mechanism
alkene oxidations
alkyne reduction reactions: Erland Stevens
alkynes acetylides
alkynes reduction
anionic addition polymers: Erland Stevens
anti-Markovnikov alkyne hydration
aromatic EAS
aromatic halogenation: Erland Stevens
aromatic predictions with Huckel's rules 1
aromatic predictions with Huckel's rules 2
base selection for making ester enolates
benzyl ether cleavage
big 4 E1 intro
big 4 E1 rearrangements
big 4 E2 acyclic halides
big 4 E2 anti beta-hydrogen and leaving group
big 4 E2 cyclic halides 1
big 4 E2 cyclic halides 2
big 4 E2 example
big 4 E2 intro
big 4 E2 other factors
big 4 E2 regiochemistry
big 4 E2 solvent
big 4 intro
big 4 SN1 E1 example
big 4 SN1 E1 intro
big 4 SN1 stereochemistry
big 4 SN1 substitution
big 4 SN2 E2 comparison
big 4 SN2 examples
big 4 SN2 intro
big 4 SN2 nucleophile
big 4 SN2 solvent
big 4 SN2 stereochemistry
big 4 SN2 sterics
bonding energy shape
bonding formaldehyde
bonding H2 energy
bonding H2 shape
bonding He2
bonding intro
Buchwald-Hartwig coupling: Erland Stevens
carbenes: Erland Stevens
carbonyl alcohol oxidation
carbonyl alkylations with LDA
carbonyl alkylations with the aldol condensation
carbonyl alkylations with the Claisen condensation
carbonyl alkylations with the Wittig reaction
carbonyl hydride examples
carbonyl hydride reagents
carbonyl intro
carbonyl organometallic examples
carbonyl organometallic intro
carbonyl organometallic reactions
carbonyl retrosynthesis
carbonyl synthesis 1
carbonyl synthesis 2
carbonyl synthesis 3
catalytic cycle for coupling reactions
cationic addition polymers: Erland Stevens
charge 2 4-chlorobenzoic acid
charge 2 proton sponge
charge electronegativity
charge hybridization
charge hyperconjugation
charge induction
charge periodic table
charge resonance 1
charge resonance 2
charge resonance acid
charge resonance formamide
charge size
Claisen condensation: Erland Stevens
comparing sound waves and orbitals
condensation polymers: Erland Stevens
conformation butane
conformation cyclohexane
conformation disubstituted cyclohexanes
conformation ethane
conformation intro
conformation line angle
conformation methylcyclohexane
conformation more rings
conformation propane
conformation rings
contrasting 1,2- and 1,4-additions
contrasting the molecular orbitals of ethylene and formaldehyde
contrasting the Wittig and Horner-Wadsworth-Emmons reaction
converting anilines to diazoniums ions
cycloadditions with azides
cycloadditions with nitrile oxides
cycloadditions with ozone
dehydration of an aldol reaction product
Dieckmann condensation: Erland Stevens
effect of degree of substitution on radical stability
endo effect in the Diels-Alder reaction
energy 1
energy 2
energy 3
enolate aldol comparison
enolate aldol condensation
enolate aldol reaction
enolate aldol reaction example
enolate alkylation: Erland Stevens
enolate bases
enolate equilibria
enolate intro
ester hydrolysis and Fischer esterification
ether cleavage with strong acids
ether synthesis through acid-catalysis
ethylene and formaldehyde - YouTube
examples of Michael additions
formation of alkoxides: Erland Stevens
formation of enolates from esters and other acid derivatives
formation of phosphonate esters with the Arbuzov reaction
Friedel-Crafts acylation: Erland Stevens
Friedel-Crafts alkylation of an aromatic ring
frontier molecular orbital analysis - YouTube
frontier molecular orbital analysis of ethylene
frontier molecular orbital analysis of formaldehyde
functional groups carbonyls
functional groups cholesterol
functional groups hydrocarbons
functional groups intro
functional groups non carbon
functional groups R groups
halogens as directing groups in aromatic reactions
HDPE - YouTube
Horner-Wadsworth-Emmons reaction to form alkenes
Huckel's rules and aromatic compounds
hybridization ammonia intro
hybridization ammonia sp2
hybridization ammonia sp3
hybridization formaldehyde
hybridization formamide
hybridization intro 1
hybridization intro 2
hybridization methane
hybridization water intro
hybridization water sp
hybridization water sp2
hybridization water sp3
importance of the enol tautomer
introduction to alpha-carbonyl alkylation
introduction to amines: Erland Stevens
introduction to biopolymers
introduction to coupling reactions
introduction to nitrogen heteroaromatic molecules
introduction to plastic recycling codes
introduction to polymers: Erland Stevens
introduction to radicals: Erland Stevens
introduction to regioselectivity in aromatic reactions
introduction to the Diels-Alder cycloaddition
keto-enol tautomerization mechanism
keto-enol tautomerization: Erland Stevens
LDPE - YouTube
line angle intro
line angle rules
line angle tips
making aryl halides
making Grignard reagents
making phosphonium salts
Markovnikov hydration of alkynes
mass spectrometry examples 1
mass spectrometry examples 2
mass spectrometry intro
mass spectrometry: alpha-cleavage
mass spectrometry: even and odd m/z values
mass spectrometry: McLafferty rearrangement
mass spectrometry: parent ion
mass spectrometry: tropylium ion
mechanism of alpha-halogenation of ketones
mechanism of amide hydrolysis
mechanism of ester hydrolysis
meta-directors in aromatic reactions
methane under hybridization - YouTube
molecular orbital theory: Erland Stevens
more on anti alkene additions
more on syn alkene additions
moving to a new YouTube home
net enolate alkylation through the aldol condensation
nitration of aromatic compounds: Erland Stevens
NMR spectroscopy: chemical shift: Erland Stevens
NMR spectroscopy: complex multiplicity
NMR spectroscopy: coupling constants
NMR spectroscopy: field strength
NMR spectroscopy: integration: Erland Stevens
NMR spectroscopy: multiplicity
NMR spectroscopy: multiplicity 2
NMR spectroscopy: nmrdorg
NMR spectroscopy: reporting data
nomenclature example 1
nomenclature example 2
nomenclature example 3
nomenclature example 4
nomenclature intro
nomenclature rules
nucleophiles that do 1,2- or 1,4-additions
nucleophilic aromatic substitutions
nucleophilicity of enamines
orbital coefficients - YouTube
orbital output data for methane - YouTube
orbitals: wave vs probability functions
ortho,para-directors in aromatic reactions
other factors that stabilize radicals
other organometallic reagents
ozonolysis: Erland Stevens
PETE - YouTube
phosphonium ylides: Erland Stevens
polynucleotides as biopolymers
polypeptides as biopolymers
polysaccharides as biopolymers
PP - YouTube
protecting groups in organic synthesis: Erland Stevens
PS - YouTube
PVC: Erland Stevens
radical addition polymers: Erland Stevens
radical additions of HX to alkenes
radical halogenation of alkanes to make alkyl halides
reaction of carbonyls with weak nucleophiles
reaction of enamines and acid chlorides
reactions of enolates of acid derivatives
reduction of aromatic ketones: Erland Stevens
reduction of nitro groups to anilines
regioselectivity in the Diels-Alder reaction: Erland Stevens
regioselectivity of radical halogenation of alkanes
resonance and regioselectivity in aromatic reactions
retrosynthesis with the Wittig reaction
s-cis conformation of diene
sample Diels-Alder reaction
SN2 reactions of enamines and alkyl halides
Sonogashira coupling: Erland Stevens
spectroscopy infrared alcohols and amines
spectroscopy infrared and conjugation
spectroscopy infrared examples 1
spectroscopy infrared examples 2
spectroscopy infrared hydrocarbons
spectroscopy infrared intro
spectroscopy IR carbonyls
spectroscopy NMR intro
stages in radical reactions
stereochemistry alkenes
stereochemistry cahn ingold prelog
stereochemistry diastereomers 1
stereochemistry diastereomers 2
stereochemistry diastereomers 3
stereochemistry drawing
stereochemistry halomethane
stereochemistry meso
stereochemistry of the diene and dienophile
stereochemistry tartaric acid
summary of different carbonyl reactions
synthesis of enamines from secondary amines and carbonyl compounds
synthesis of imines from primary amines and carbonyl compounds
synthesis of isoxazoles
synthesis of primary amines by SN2 reactions
synthesis of pyrazoles
synthesis of secondary amines: Erland Stevens
synthesis of tertiary amines: Erland Stevens
synthesis of thiazoles
the Michael reaction: Erland Stevens
the Wittig reaction versus the E1 and E2 eliminations
the Wittig reaction: Erland Stevens
THP ether protecting group
THP group for protecting alcohols
transformations of diazonium ions
uses for alpha-halogenated carbonyl compounds
visualizing alkenes as carbonyl precursors
Welcome to my organic chemistry tutorial channel!
Williamson ether synthesis: Erland Stevens
x 1,3-dipolar cycloadditions: Erland Stevens
x 1,3-dipoles