New Organic Chemistry Playlist
Basic studies, Trigonometry
New Organic Chemistry Playlist
138 Lessons
- Organic Chemistry For College Students - Basic Introduction
- Organic Chemistry – How To Draw Lewis Structures
- Ionic Bonds, Polar Covalent Bonds, and Nonpolar Covalent Bonds
- Which Bond Is More Polar?
- Formal Charge
- Predicting Bond Angles
- Kekule Structures and Condensed Structures
- VSEPR Theory – Basic Introduction
- Molecular Geometry & VSEPR Theory – Basic Introduction
- Valence Bond Theory & Hybrid Atomic Orbitals
- Bond Strength and Bond Length
- Dipole Moment, Molecular Polarity & Percent Ionic Character
- Intermolecular Forces – Hydrogen Bonding, Dipole Dipole Interactions – Boiling Point & Solubility
- pKa, Ka, and Acid Strength
- Conjugate Acids and Bases
- Using Pka Values To Predict The Position of Equilibrium & The Products of an Acid Base Reaction
- Curved Arrow Notation For Acid Base Reaction Mechanisms
- Acids and Bases – Electronegativity, Atomic Size, Hybridization, Resonance & Inductive Effect
- Lewis Acids and Bases
- Nucleophiles and Electrophiles
- The Effect of pH on Acid Structure
- Hydrocarbons – Aliphatic vs Aromatic Molecules – Saturated & Unsaturated Compounds
- Functional Groups
- Organic Chemistry Drawing Structures – Bond Line, Skeletal, and Condensed Structural Formulas
- Naming Organic Compounds – IUPAC Nomenclature of Alkanes
- Naming Alkanes With Branched Substituents – IUPAC Nomenclature
- Constitutional Isomers
- Resonance Structures
- Naming Cycloalkanes With Substituents, Cis & Trans, Bicyclo Alkane Nomenclature
- Naming Bicyclic Compounds
- Naming Ethers – IUPAC Nomenclature With Branching, Organic Chemistry Practice Problems
- Naming Alcohols – IUPAC Nomenclature
- Naming Alkyl Halides – IUPAC Nomenclature
- Naming Amines – IUPAC Nomenclature & Common Names
- Van Der Waals Forces
- Boiling Point of Organic Compounds
- Ring Flips
- Newman Projections
- Chair Conformation
- Stability of Cycloalkanes – Angle Strain
- Cis and Trans Isomers
- Finding Chirality Centers
- R and S Configuration – Stereochemistry
- Fischer Projections – Stereochemistry
- Enantiomers
- Diastereomers
- Meso Compounds
- Stereoisomers
- Specific & Observed Rotation, Optically Active, Enantiomeric Excess, Chiral & Achiral Molecules
- Naming Alkenes Using E Z System – IUPAC Nomenclature
- Degree of Unsaturation and Index of Hydrogen Deficiency
- Hydrohalogenation – Alkene Reaction Mechanism
- Hydration of Alkenes Reaction Mechanism
- Oxymercuration Demercuration Reaction Mechanism
- Alkoxymercuration Demercuration Reaction Mechanism
- Hydroboration – Oxidation Reaction Mechanism
- Halogenation of Alkenes & Halohydrin Formation Reaction Mechanism
- Epoxidation of Alkenes
- Alkene + KMnO4 Reaction
- Ozonolysis – Oxidative Cleavage of Alkenes
- Alkene Reactions – Fast Review!
- Naming Alkynes – IUPAC Nomenclature & Common Names
- Alkyne Reactions – Quick Review!
- SN2 SN1 E1 E2 Reaction Mechanisms Made Easy!
- SN2 Reaction Mechanism With Stereochemistry, Chair Conformation & Fischer Projection Problems
- SN1 Reaction Mechanism – Carbocation Rearrangements, Solvolysis & Racemic Mixtures
- Carbocation Stability – Hyperconjugation, Inductive Effect & Resonance Structures
- Polar Protic Solvents and Polar Aprotic Solvents For SN1 & SN2 Reactions
- E1 Reaction Mechanism With Alcohol Dehydration & Ring Expansion Problems
- E2 Reaction Mechanism – Hoffman Elimination vs Zaitsev’s Rule
- E2 Stereochemistry With Newman Projections
- Organic Chemistry – Reactions of Alcohols – PBr3, SOCl2, HBr & Tosylation
- E1 & E2 Dehydration of Alcohols Into Alkenes – Acid Catalyzed Elimination Reaction Mechanism
- Oxidation of Alcohols – PCC, H2CrO4 & Swern Oxidation
- Williamson Ether Synthesis Reaction Mechanism
- Ether and Epoxide Reactions
- Free Radical Reactions of Alkanes & Alkenes With NBS
- Kinetic vs Thermodynamic Product – 1,2 vs 1,4 Addition of HBr to 1,3 Butadiene
- Diels Alder Reaction
- Aromatic, Antiaromatic, or Nonaromatic – Huckel’s Rule, 4n+2 – Heterocycles & Aromaticity
- Naming Carboxylic Acids – IUPAC Nomenclature
- Naming Esters – IUPAC Nomenclature, Branches, Substituents, & Benzene Rings – Organic Chemistry
- Naming Acid Anhydrides and Nitriles – IUPAC Nomenclature
- Naming Acid Chlorides With IUPAC Nomenclature
- Naming Amides – IUPAC Nomenclature
- Carboxylic Acid Derivative Reactions
- Naming Aldehydes Explained, IUPAC Nomenclature Practice – Organic Chemistry
- Naming Ketones Explained – IUPAC Nomenclature Practice & Examples – Organic Chemistry
- NaBH4, LiAlH4, DIBAL Reduction Mechanism, Carboxylic Acid, Acid Chloride, Ester, & Ketones
- Grignard Reagent Reaction Mechanism
- Aldehydes and Ketones
- Keto Enol Tautomerism – Acid & Base Reaction Mechanism, Tautomerization, Organic Chemistry
- Alpha Halogenation of Ketones
- Imine and Enamine Formation Reactions With Reductive Amination
- Protecting Groups, Acetals, and Hemiacetals
- Wittig Reaction Mechanism
- Naming Benzene Derivatives – Aromatic Compounds
- Aromatic Halogenation Mechanism – Chlorination, Iodination & Bromination of Benzene
- Nitration of Benzene Mechanism – Electrophilic Aromatic Substitution Reactions
- Sulfonation of Benzene & Desulfonation Reaction Mechanism – Aromatic Compounds
- Friedel Crafts Acylation of Benzene Reaction Mechanism
- Gatterman Koch Reaction
- Friedel Crafts Alkylation of Benzene Reaction Mechanism – Tons of Examples!
- Clemmensen Reduction, Wolff Kishner Mechanism, Thioketal Mozingo Reaction, Organic Chemistry
- Benzene Side Chain Reactions
- Ortho Meta Para Directors – Activating and Deactivating Groups
- Nitration of MethylBenzoate and Nitration of Bromobenzene
- Ortho Para Ratio – Aromatic Nitration of Toluene
- Electrophilic Aromatic Substitution Reactions Made Easy!
- Nucleophilic Aromatic Substitution – Benzyne Intermediate and Meisenheimer Complex
- Arenediazonium Salts With Diazo Coupling and Sandmeyer Reactions
- Enolate Reactions – Direct Alkylation of Ketones With LDA
- Aldol Addition Reactions, Intramolecular Aldol Condensation Reactions, Retro Aldol & Cross Aldol Rea
- Michael Addition Reaction Mechanism
- Robinson Annulation Reaction Mechanism
- Stork Enamine Reaction Mechanism – Alkylation, Acylation, & Michael Addition
- Claisen Condensation Reaction Mechanism
- Dieckmann Condensation Reaction Mechanism
- Malonic Ester Synthesis Reaction Mechanism
- Acetoacetic Ester Synthesis Reaction Mechanism
- Decarboxylation Reaction Mechanism
- Amine Synthesis Reactions
- Aromatic Compounds & Heterocycles – Nucleophilic & Electrophilic Aromatic Substitution Reactions
- Introduction to Organometallic Compounds
- Carbohydrates – Haworth & Fischer Projections With Chair Conformations
- Organic Chemistry Reactions Summary
- Organic Chemistry – Reaction Mechanisms
- Mass Spectrometry
- Shielding and Deshielding – H NMR Spectroscopy
- Basic Introduction to NMR Spectroscopy
- How To Determine The Number of Signals In a H NMR Spectrum
- Chemical Shift In NMR Spectroscopy
- Diamagnetic Anisotropy – H NMR Spectroscopy – Organic Chemistry
- Integration of H NMR Signals – Spectroscopy – Organic Chemistry
- Spin Spin Splitting – N+1 Rule – Multiplicity – Proton NMR Spectroscopy
- How To Draw The Proton NMR Spectrum of an Organic Molecule
- Proton NMR Spectroscopy – How To Draw The Structure Given The Spectrum
- Carbon-13 NMR Spectroscopy
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1 2 addition
1 3 butadiene
1 4 addition
2 3 dimethylpentane
4n+2
acetals
acetoacetic ester synthesis
acetone
achiral molecules
acid
acid base reaction mechanisms
acid base reactions
acid catalyzed
acid chloride
Acid strength
acid structure
Acid--base Reaction
acidic
acids
acids and bases
activating groups
Acylation
alcohol
alcohol dehydration
alcohol reactions
alcohols
Aldehyde
aldehyde nomenclature
aldehydes
aldehydes and ketones
aldol addition
aldol addition reaction
aldol condensation
aldol condensation reaction
aldol reaction
aliphatic hydrocarbons
alkane
alkanes
alkene + KMnO4
alkene reaction mechanism
alkene reactions
alkenes
alkoxymercuration demercuration
Alkylation
alkyne reactions
alpha halogenation
alpha halogenation of ketones
amide
amine
amine synthesis reactions
amines
angle strain
anti conformation
antiaromatic
aprotic solvents
arenediazonium salts
aromatic
aromatic antiaromatic nonaromatic
aromatic compounds
aromatic halogenation
aromatic halogenation mechanism
aromatic hydrocarbons
aromatic substitution
aromaticity
atomic orbitals
atomic size
azo compounds
base
base catalyzed
bases
Basic
basic introduction
bent
Benzene
benzene derivatives
benzene rings
benzyne intermediate
beta keto acids
bicyclic alkanes
bicyclic compounds
bicyclo alkanes
boiling point
boiling point of organic compounds
bond angles
bond length
bond strength
bond-line structures
branched substituents
branches
branching
bromination
bromination of benzene
butane
C NMR
calculations
carbocation rearrangements
carbocation stability
carbohydrates
carbon-13 NMR spectroscopy
carboxylic acid
carboxylic acid derivative reactions
carboxylic acid derivatives
carboxylic acids
Catalyst
chair conformation
chemical shift
chemistry
chiral
chiral and achiral molecules
chiral centers
chiral molecules
chiral vs achiral
Chirality
chirality centers
chlorination
cis
cis and trans
cis and trans isomers
Claisen condensation
claisen condensation reaction
claisen condensation reaction mechanism
clemmensen
Clemmensen reduction
college students
common names
compounds
condensed structural formula
condensed structures
conditions
conformational analysis
conjugate acids
conjugate acids and bases
conjugate bases
conjugation
constitutional isomers
Coupling
covalent bonds
cross aldol reaction
curved arrow notation
curved arrows
cycloalkanes
cyclobutane
cycloheptane
cyclohexane
cyclooctane
cyclopentane
cyclopropane
deactivating groups
decarboxylation
decarboxylation reaction mechanism
degree of unsaturation
dehydration of alcohols
dept nmr
deshielding
desulfonation
desulfonation reaction mechanism
dextrorotatory
diamagnetic anisotropy
diastereomers
diazo coupling
DIBAL
Dibal mechanism
Dibal reduction
dieckmann condensation
dieckmann condensation reaction
dieckmann condensation reaction mechanism
Diels-Alder reaction
diesters
dione
dipole
dipole dipole interactions
dipole moment
direct alkylation of ketones
double bond
doublet
drawing bond line structures
drawing condensed structures
drawing line structures
drawing skeletal structures
drawing structural formulas
drawing structures
E Z system
E1
E1 reaction
E1 reaction mechanism
E2
E2 reaction
E2 reaction mechanism
E2 stereochemistry
eclipsed conformation
electronegativity
electrophiles
Electrophilic Aromatic Substitution
electrophilic aromatic substitution reactions
elimination
enamine
enamines
enantiomeric excess
enantiomers
enol
enol keto tautomerization
enolate reactions
epoxidation
epoxide reactions
equilibrium
ester
esters
esters nomenclature
esters organic chemistry
Ethane
ethers
ethers and epoxides
ethers nomenclature
examples
explained
finding chirality centers
Fischer projection
fischer projections
Formal Charge
free radical reactions
free radicals
Friedel-Crafts acylation
Friedel-Crafts alkylation
full mechanism
functional groups
gatterman koch reaction
gauche conformation
Grignard reagent
H NMR
h2cro4
H2N-NH2
halides
halogenation
halogenation of alkenes
halogens
halohydrin formation
haworth projection
HBr
hcl
hemiacetals
heterocycles
hoffman
how to draw
how to draw lewis structures
Hückel's rule
hybrid atomic orbitals
hybridization
hydration of alkenes
hydration of alkenes reaction mechanism
hydrazine
hydroboration/oxidation
hydrocarbons
hydrogen bond
hydrogen bonding
hydrohalogenation
hyperconjugation
imines
index of hydrogen deficiency
inductive effect
Integration
intermolecular forces
intramolecular
intramolecular aldol reaction
Introduction
iodination
ionic bonds
ionic character
isomers
IUPAC
iupac nomenclature
iupac nomenclature of alkanes
kā
kekule structures
keto
keto-enol tautomerism
Ketone
ketones
ketones chemistry
ketones explained
ketones nomenclature
ketones organic chemistry
kinetic vs thermodynamic product
KMnO4
LDA
least polar
levorotatory
lewis acid
lewis acids and bases
lewis base
Lewis structures
LiAlH4
LiAlH4 carboxylic acid
LiAlH4 mechanism
LiAlH4 reduction mechanism
line structures
linear
malonic ester synthesis
mass spectrometry
Mechanism
meisenheimer complex
meso compounds
Michael addition
michael addition reaction
michael addition reaction mechanism
michael reaction
mild
molecular geometry
molecular polarity
molecular structure
Molecule
most polar
mozingo
mozingo reduction
multiplet
multiplicity
n+1 rule
N2H4
NaBH4
NABH4 reduction mechanism
naming
naming acid anhydrides
naming acid chlorides
naming alcohols
naming aldehydes
naming alkanes
naming alkanes with branched substituents
naming alkenes
naming alkenes using e z system
naming alkyl halides
naming alkynes
naming amides
naming amines
naming benzene derivatives
naming bicyclic compounds
naming carboxylic acids
naming cycloalkanes
naming cycloalkanes with substitutents
naming cycloalkenes
naming esters
naming esters examples
naming esters iupac
naming esters organic chemistry
naming esters with benzene ring
naming esters with branches
naming esters with substituents
naming ethers
naming ethers examples
naming ethers iupac
naming ethers organic chemistry
naming ethers practice
naming ethers practice problem
naming ethers with branches
naming ketones
naming nitriles
naming organic compounds
NBS
Newman projections
nitration
nitration of benzene
nitration of bromobenzene
nitration of methylbenzoate
nitration of toluene
NMR
nmr spectroscopy
nomenclature
nonaromatic
nonpolar
nonpolar covalent bonds
nucleophiles
nucleophiles and electrophiles
nucleophilic addition reactions
Nucleophilic Aromatic Substitution
number of signals
observed rotation
octahedral
optical properties
optical purity
optically active
Orbitals
organic chemistry
organic chemistry condensed structure
organic chemistry drawing structures
organic chemistry drawing structures practice
organic chemistry line structures
organic chemistry skeletal structures
organic compounds
organometallic compounds
ortho meta para directors
ortho para ratio
Oxidation
oxidation of alcohols
oxidative cleavage of alkenes
oxymercuration demercuration
ozonolysis
PBr3
pcc
percent ionic character
pH
phenol
pKa
pKa values
plane polarized light
Polar
polar aprotic solvents
polar bonds
polar covalent bonds
polar protic solvents
polarimeter
polarity
position of equilibrium
practice
practice problems
predicting bond angles
problems
products
protecting groups
protic solvents
Proton NMR
proton nmr spectroscopy
Quartet
quintet
R and S configuration
racemic mixture
radical reactions
raney Ni
raney nickel
Reaction
reaction mechanism
reaction mechanisms
reaction summary
reactions
reactions of alcohols
reactions of ethers
reduction
reductive amination
resonance
resonance structures
retro aldol reaction
retro-aldol
Ring
ring expansion
ring flip
ring flip chair conformation
ring flip cyclohexane
ring flip organic chemistry
ring strain
Robinson Annulation
robinson annulation mechanism
Rules
sandmeyer reactions
saturated hydrocarbons
seesaw
selective reduction
septet
sextet
shielding
side chain oxidation
side chain reactions
sigma and pi bonds
Signals
singlet
skeletal structures
SN1
SN1 reaction
SN1 reaction mechanism
sn1 reactions
SN2
sn2 reaction mechanism
sn2 reactions
sn2 sn1 e1 e2
SOCl2
solubility
solvolysis
specific rotation
spectroscopy
spectrum
spin-spin splitting
splitting
square planar
square pyramidal
stability
stability of cycloalkanes
staggered conformation
stereochemistry
stereoisomers
stork enamine
stork enamine reaction
Structure
substituents
sulfonation
sulfonation of benzene
swern oxidation
t-shape
tautomer
tautomerism
tautomerization
Tetrahedral
the effect of pH on acid structure
thioketal
thioketal reduction
Tosylation
Trans
trigonal bipyramidal
trigonal planar
trigonal pyramidal
triplet
tutorial
unsaturated hydrocarbons
valence bond theory
van der waals forces
video
VSEPR
VSEPR Theory
vsepr theory and molecular geometry
vsepr theory practice problems
which bond is more polar
Williamson ether synthesis
wittig reaction mechanism
wolff kishner
wolff kishner mechanism
wolff kishner reaction
wolff kishner reaction mechanism
wolff kishner reduction mechanism
Wolff-Kishner reduction
zaitsev's rule
Zn(Hg)