Organic Chemistry Video Tutorial Playlist
Lección 86 de 136 · Kinetic vs Thermodynamic Product: 1,2 vs 1,4 addition of bromine Br2 to 1,3 butadiene · Estudios básicos
Kinetic vs Thermodynamic Product: 1,2 vs 1,4 addition of bromine Br2 to 1,3 butadiene
This video discusses the 1,2 and 1,4 addition of Bromine Br2 to 1,3-butadiene. It discusses the difference between the kinetic product and thermodynamic product and how to identify them whenever you have 2 or 4 different products by analyzing the carbocation intermediate and the relative stability of the alkene product. The kinetic product is the major product under low temperature conditons and the thermodynamic product is the major product under high temperature conditions.
- 1 2 addition
- 1 3 butadiene
- 1 3-cyclohexadiene
- 1 4 addition
- 1 5 dicarbonal compounds
- 1 5 dicarbonyl compound
- 1 5 dicarbonyl product
- 2 different products
- 2-pentanol
- 200-400nm
- 4 different products
- 4+2 cycloaddition
- 4n+2
- absorption
- acceptor
- acetaldehyde
- acetic acid pka
- acetoacetic
- acetoacetic ester
- acetoacetic ester synthesis
- acetoacetic ester synthesis mechanism
- acetone
- acetone and acetaldehyde
- acetylene pka
- acid
- acid anhydride
- acid catalysis
- acid catalyzed
- acid catalyzed acetoacetic ester synthesis
- acid catalyzed cleavage of epoxides
- acid catalyzed cleavage of ethers
- acid catalyzed dehydration
- acid catalyzed hydration
- acid catalyzed mechanism
- acid catalyzed michael addition reaction mechanism
- acid chloride
- acid chlorides
- acid hydrolysis
- Acid strength
- acidic
- acidic conditions
- acidic mechanism
- Acidity
- acidity of alcohols
- acidity of alkynes
- acidity of carboxylic acids
- acidity of phenols
- activating and deactivating groups
- acyl chloride
- Acylation
- acylinium ion
- addition of hydrogen halide
- AlCl3
- alcohol
- alcohol + h2so4
- alcohol + h2so4 mechanism
- alcohol + sulfuric acid
- alcohol dehydration
- alcohol dehydration mechanism
- alcohol dehydration reaction
- alcohols
- Aldehyde
- aldehydes
- aldehydes and ketones
- aldehydes and ketones exam review
- aldehydes and ketones naming
- aldehydes and ketones nomenclature
- aldehydes and ketones nucleophilic addition
- aldehydes and ketones organic chemistry
- aldehydes and ketones properties
- aldol
- aldol condensation
- aldol condensation mechanism
- aldol condensation reaction
- aldol reaction
- aldol reaction examples
- aldol reaction mechanism
- aldol reaction problems
- aldol retrosynthesis
- alkane
- alkanes
- alkene addition reactions
- alkene reactions
- alkene stability
- alkene to alcohol
- alkene to aldehyde
- alkene to alkane
- alkene to alkyl halide
- alkene to cis diol
- alkene to cyclopropane
- alkene to ether
- alkene to ketone
- alkene to trans diol
- alkenes
- alkyl bromide
- alkyl halide
- Alkylation
- alkyne addition reactions
- alkyne carbanions
- alkyne reagents
- alkyne synthesis reactions
- alkynes
- allylic carbanion
- allylic carbocation
- alpha beta unsaturated aldehyde
- alpha beta unsaturated ketone
- alpha beta unsaturated ketones
- alpha hydrogen
- Amides
- amines
- anhydride
- anhydrides
- aniline
- annulation
- anthracene
- anti
- anti diol
- antiaromatic
- antiaromaticity
- aprotic solvents
- aromatic
- aromatic antiaromatic nonaromatic
- aromatic ring
- aromaticity
- arrow pushing mechanism
- arrows
- base catalyzed cleavage of epoxides
- benzaldehyde
- Benzene
- benzylic carbocation
- benzyne intermediate
- beta hydroxy ketone
- beta keto ester
- Br2
- bromination
- bromine
- carbocation intermediate
- carboxylate
- carboxylation
- carboxylic acid
- carboxylic acid derivative mechanisms
- carboxylic acid derivatives
- carboxylic acids
- CH3OH pka
- Channel
- chiral carbon center
- chiral carbon centers
- chirality center
- chlorination
- cis alkene
- cis and trans
- cis trans geometric isomers
- Cl2
- claisen
- Claisen condensation
- claisen condensation mechanism
- claisen condensation reaction
- claisen mechanism
- claisen reaction
- claisen schmidt mechanism
- claisen schmidt reaction
- CO2
- condensation
- conformation
- conjugated
- conjugated alkenes
- constitutional isomers
- crossed aldol condensation
- crossed aldol condensation reaction
- cyclic alpha beta unsaturated ketone
- cyclic claisen condensation
- cyclic ketones
- cyclobutadiene
- cycloheptatrienyl
- cyclohexane
- cyclohexane carboxylic acid
- cyclohexanoic acid
- cyclohexanone
- cyclohexatrienyl
- cyclooctatetraene
- cyclopentadiene
- cyclopentadienyl
- cyclopentane
- cyclopentane carboxylic acid
- cyclopentanoic acid
- cyclopentylmagnesium bromide
- D2O
- decarboxylation
- dehydration
- dehydration of alcohols
- delocalization
- diastereomers
- dieckmann
- dieckmann condensation
- dieckmann condensation examples
- dieckmann condensation mechanism
- dieckmann condensation problems
- dieckmann reaction
- Diels-Alder reaction
- diene
- dienes
- dienophile
- direct alkylation
- donors
- E Z isomers
- E1
- E1 mechanism
- e1cb
- E2
- e2 mechanism
- electron donating and electron withdrawing groups
- electron donating group
- electron pushing
- electron withdrawing group
- electron withdrawing groups
- electrophile
- electrophilic addition reaction
- Electrophilic Aromatic Substitution
- electrophilic aromatic substitution reactions
- electrophilic radical substitution
- elimination reaction
- enamine
- enantiomers
- enantiomers and meso compounds
- enol
- enolate
- enolate alkylation
- enolate chemistry
- enolate formation
- enolate ion
- enolate ions
- enolate reactions
- epoxide
- epoxides
- ester
- esters
- ethanol pka
- ethers
- ethers and epoxides
- ethyl acetate
- ethylene oxide
- ethylmagnesium bromide
- examples
- extra credit
- FeBr3
- final exam review
- fischer projections
- fischer projections nomenclature
- Formal Charge
- Formaldehyde
- four products
- Friedel-Crafts acylation
- Friedel-Crafts alkylation
- functional groups
- furan
- gamma hydrogen
- gatterman koch reaction
- grignard reaction
- Grignard reagent
- grignard reagent reaction
- grignard reagent synthesis
- h2 pt
- h2cro4
- H2O
- H2SO4
- H3O+
- halogenation
- HBr
- hbr h2o2
- hcl
- heat
- heterocycles
- hgso4
- hgso4 h2o h2so4
- high electron density
- high temperature
- HNO3
- homework problems
- HONO
- how to draw resonance structures
- how to get an A in organic chemistry
- how to name organic compounds
- how to pass organic chemistry
- huckel's number
- Hückel's rule
- hydration of aldehydes and ketones
- hydroboration/oxidation
- hydrolysis
- hydrolysis and decarboxylation
- imidazole
- imine
- intramolecular
- intramolecular aldol condensation
- intramolecular aldol condensation mechanism
- intramolecular aldol condensation reaction
- intramolecular claisen condensation
- intramolecular reaction
- iodination
- isopropanol acidity
- Ketone
- ketones
- key points
- kinetic product
- KMnO4
- kmno4 h3o+
- knoevenagel
- Knoevenagel Condensation
- knoevenagel condensation mechanism
- lactones
- LDA
- learn organic chemistry
- li nh3
- Lindlar catalyst
- lindlar's catalyst
- low temperature
- major and minor contributor
- major product
- major resonance contributor
- maleic anhydride
- malonic acid
- malonic ester
- malonic ester mechanism
- malonic ester reaction
- malonic ester synthesis
- malonic ester synthesis mechanism
- malonic ester synthesis reaction
- malonitrile
- markovnikov and anti markovnikov
- Mechanism
- mechanism problems
- meisenheimer complex
- Meso
- meso compounds
- methyl ketones
- methyl vinyl ketone
- methylmagnesium bromide
- michael acceptor
- michael acceptor and donor
- michael acceptors
- Michael addition
- michael addition examples
- michael addition reaction
- michael addition reactions
- michael additon mechanism
- michael donor
- michael donors
- michael reaction
- michael reaction examples
- michael reaction mechanism
- michael reaction problems
- michael reaction retrosynthesis
- Na and NH3
- na nh3
- nanh2
- NaNO2
- NaOEt
- naphthalene
- Newman projections
- nitration
- nitriles
- nitrobenzene
- nomenclature
- nonaromatic
- nucleophile
- nucleophilic addition reaction
- nucleophilic addition reactions
- Nucleophilic Aromatic Substitution
- Nucleophilic substitution
- number of stereoisomers
- o3
- o3 h2o
- old exams
- organic chemistry
- organic chemistry 1
- organic chemistry 1 final exam review
- organic chemistry functional groups
- organic chemistry functional groups naming
- organic chemistry functional groups nomenclature
- organic chemistry functional groups review
- organic chemistry practice tests
- organic chemistry reaction mechanisms
- organic chemistry study tops
- organic chemistry tutor
- organic compounds
- ortho para meta directors
- Oxidation
- oxidation or reduction
- oxymercuration demercuration
- ozonolysis
- Patreon
- patreon channel
- patreon review
- patreon rewards
- patreon rewards tutorial
- patreon tutorial
- patreon tutorial video
- patreon video
- pcc
- Pd baso4
- phenols
- phenoxide
- phenylmagneisum bromide
- piperidine
- pKa
- pka acidity
- polar aprotic solvent
- polar protic solvent
- polyenes)
- practice
- practice problems
- practice test
- predict the major product
- primary alcohol
- primary alcohols
- problems
- propanal
- protic solvents
- purine
- pyrimidine
- pyrrole
- r and s
- R and S configuration
- R and S nomenclature
- R group
- Reaction
- reaction mechanism
- reactions
- reactions of alkynes
- reactivity
- reactivity of aldehydes and ketones
- rearrangement reaction
- reduction
- resonance stabilization of the conjugate base
- resonance structures
- retro
- retro aldol mechanism
- retro aldol reaction
- retro-aldol
- retrosynthesis
- review
- rewards
- ring closing
- ring closing example
- Robinson Annulation
- robinson annulation mechanism
- robinson annulation practice
- robinson annulation practice problems
- robinson annulation problems
- robinson annulation reaction
- robinson annulation retrosynthesis
- s character
- s-cis
- s-trans
- Sandmeyer reaction
- secondary alcohol
- secondary alcohols
- sia2bh
- SN1
- sn1 and sn2 reactions
- SN1 reaction
- sn1 sn2 e1 e2
- sn1 sn2 e1 e2 made easy
- sn1 vs sn2
- SN2
- SN2 reaction
- sn2 reaction mechanism
- sodium ethoxide
- sp hybrid orbitals
- spectroscopy
- stability
- stability of alkene
- stereocenters
- stereochemistry
- stereochemistry of organic compounds
- stereochemistry r and s
- Stork
- stork enamine alkylation
- stork enamine mechanism
- stork enamine reaction
- stork reaction
- study guide
- substituted carboxylic acid
- substituted carboxylic acids
- substituted ketone derivatives
- substituted ketones
- substitution reaction
- sulfonation
- sulfuric acid
- syn and anti addition
- syn diol
- synthesis
- synthesis of aldehydes and ketones
- tautomerism
- tertiary alcohol
- tertiary alcohols
- thermodynamic product
- thiazole
- thiols
- thiophene
- trans alkene
- tropylium ion
- tutorial
- tutorial video
- ultraviolet radiation.
- unsaturated ketone
- UV
- UV radiation
- UV spectroscopy
- uv spectroscopy analysis
- uv spectroscopy organic chemistry
- uv-vis spectroscopy
- video
- vis
- water
- wavelength
- Wittig reaction
- ylides