Organic Chemistry Mechanisms 10.0
Paid Version
Publisher Description
This is the second version of Organic Chemistry Mechanisms. Due to me using a second software update kit, I cannot update my old app and update it and retain my 1,000+ down loaders. So to get my user base back, I am offering versions 2.0 of this app for %50 OFF!!!
MCAT, College Organic Chemistry. This app covers summaries and detailed electron pushing diagrams of all of the following topics. Best viewed in Landscape Mode.
Every single "-" below includes a description and a detailed reaction mechanism.
Alkanes
- Thermal Cracking - Pyrolysis
- Combustion
- Free Radical Halogenation
Alkenes
- Electrophilic Addition of HX to Alkenes
- Acid Catalyzed Hydration of Alkenes
- Electrophilic Addition of Halogens to Alkenes
- Halohydrin Formation
- Free Radical Addition of HX to Alkenes
- Catalytic Hydrogenation of Alkenes
- Oxidation of Alkenes to Vicinal Diols
- Oxidative Cleavage of Alkenes
- Ozonolysis of Alkenes
- Allylic Halogenation
- Oxymercuration-Demercuration
- Hydroboration of Alkenes
Alkynes
- Electrophilic Addition of HX to Alkynes
- Hydration of Alkynes
- Free Radical Addition of HX to Alkynes
- Electrophilic Halogenation of Alkynes
- Hydroboration of Alkynes
- Catalytic Hydrogenation of Alkynes
- Reduction of Alkynes with Alkali Metal - Ammonia
- Formation and Use of Acetylide Anion Nucleophiles
Alkyl Halides
- Coupling of Alkyl Halides with Gilman Reagents
- SN2 Mechanism with Alkyl Halides
- SN1 Mechanism with Alkyl Halides
- E2 Mechanism with Alkyl Halides
- E1 Mechanism with Alkyl Halides
Conjugated Species
- SN1 Mechanism with Allylic Cation Intermediate
- 1,2 and 1,4 Addition to Conjugated Diene
- Diels-Alder Reaction
Aromatic Compounds
- Electrophilic Aromatic Substitution with Halogen
- Electrophilic Aromatic Substitution - Nitration
- Electrophilic Aromatic Substitution - Sulfonation
- Friedel-Crafts Alkylation
- Friedel-Crafts Acylation
- Nucleophilic Aromatic Substitution
- Alkylbenzene Oxidation
- Alkylbenzene Halogenation
Alcohols & Ethers
- Electrophilic Aromatic Substitution with Halogen
- Electrophilic Aromatic Substitution - Nitration
- Electrophilic Aromatic Substitution - Sulfonation
- Friedel-Crafts Alkylation
- Friedel-Crafts Acylation
- Nucleophilic Aromatic Substitution
- Alkylbenzene Oxidation
- Alkylbenzene Halogenation
Alcohols & Ethers
- Dehydration of Alcohols
- Reaction of Alcohols with HX – Dehydrohalogenation
- Reaction of Alcohols with Thionyl Chloride
- Reaction of Alcohols with Phosphorus Tribromide
- Oxidation of Alcohols
- Alkoxide Ion Formation from Alcohols
- Reaction of Alcohols to form Ethers
- Williamson Ether Synthesis
- Acid Cleavage of Ethers
- Epoxidation of Halohydrins
- Acid Epoxide Ring Opening
Aldehydes & Ketones
- Reduction of Ketones and Aldehydes
- Reduction of Aryl Alkyl Ketones
- Oxidation of Aldehydes and Ketones
- Reaction of Grignard Reagents with Aldehydes and Ketones
- The Wittig Reaction
- Acetal Formation
- The Wolff-Kishner Reaction
- Reductive Amination
- The Cannizzaro Reaction
- Acid or Base Catalyzed Enolization
- Alpha Halogenation
- Haloform Reaction of Methyl Ketones
- Aldol Condensation
- Conjugate Nucleophilic Addition
- Conjugate Addition of Gilman Reagents
Carboxylic Acid Derivatives
- Reduction of Ketones and Aldehydes
- Reduction of Aryl Alkyl Ketones
- Oxidation of Aldehydes and Ketones
- Reaction of Grignard Reagents with Aldehydes and Ketones
- The Wittig Reaction
- Acetal Formation
- The Wolff-Kishner Reaction
- Reductive Amination
- The Cannizzaro Reaction
- Acid or Base Catalyzed Enolization
- Alpha Halogenation
- Haloform Reaction of Methyl Ketones
- Aldol Condensation
- Conjugate Nucleophilic Addition
- Conjugate Addition of Gilman Reagents
About Organic Chemistry Mechanisms
Organic Chemistry Mechanisms is a paid app for Android published in the Teaching & Training Tools list of apps, part of Education.
The company that develops Organic Chemistry Mechanisms is Blackbird Systems Software. The latest version released by its developer is 10.0. This app was rated by 1 users of our site and has an average rating of 5.0.
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