Please enable JavaScript.
Coggle requires JavaScript to display documents.
Reaction mechanisms (organic reaction mechanism (polar reactions (Addition…
Reaction mechanisms
organic reaction mechanism
cleavage
heterolytic
homolytic
reactive intermediates
Carbocations and cabanions
Carbocation
Cabanion
Inductive effects
Mesomeric effects
Steric effects
Nucleophile and Electrophile
Redox reactions
polar reactions
Addition reactions
Elimination reactions
Substitution reaction
Radical reactions
Selectivity
types of reactions
Electrophilic Addition
Alkenes
Alcohols
Alkyl halides
Unsymmetrical Alkenes
Markovnikov Rule
Stability of carbocations
Elimination
E1
E2
Nucleophilic Substitution
Reactions of Nucleophiles with Alkyl Halides
Sn1
Sn2
Comparism of Sn1 and Sn2
Oxidation
Alcohols
Aldehydes
Ketones
Carboxylic Acids
Oxidising Agents
Two mechanisms
Nucleophilic Cabronyl Addition
Reduction of C=O
Hemiacetals
Acetals
Keto-Enol Tautomerism
Enolate Ion
Aldol Condensation
Halogenalkanes
Halogination of alkanes
Halogination of alcohols
with hydrogen halides
with phosphorus trihalides
with thionyl chloride
with 4-toluenesulfonyl chloride
nucleophilic Substitution of halogenalkanes
Sn1
Sn2
Elimination mechanisms
E1
E2
Enantiomers
R-Convention
S-Convention
Priority Rules
Fischer-Projection
Key concepts
Electronegativity
Electrophile and nucleophile
Curved arrowes
Regioselectivity
Alkenes and Alkynes
Hyperconjugation
Electrophilic addition
Alkenes
Addition of hydrogen halides
Addition of bromine
Anti addition
in the presence of water
in the presence of water
Addition of water in the presence of acid
Hydration of unsymmetrical alkenes
Pericyclic reactions
Alkynes
Addition of hydrogen Halides
Preparation of alkynes
By partial reduction of alkynes using a Lindlar catalyst
By partial reduction of alkynes using sodium in liquid amonia
Alkynes
Aldehydes and Ketones
Nucleophilic Addition reaction
relative reactivity
Reaction with hydrides
Using complex metal hydrides
Cannizzaro reaction
Reaction with Carbon nucleophiles
Reaction with organometallics to form alcohols
The Wittig reaction
Reaction with Oxygen nucleophiles
Addition of alcohols from hemiacetals and acetals
Formation of acetals
reactions on the presence of an acid catalyst
Acetals as a protecting group
Reaction with Sulfur nucleophiles
reaction with Nitrogen nucleophiles
Alpha Substitution reactions
Keto-enol Tautomerism
Reactions of enols with electrophiles
Reaction of enolate Ions with electrophiles
Carbonyl-Carbonyl condensation reactions
Aldol condensation
Crossed Aldol condensation
Intramolecular Aldol condensation