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Organic Chemistry 1.1

1 MB / 0+ Downloads / Rating 5.0 - 1 reviews


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Organic Chemistry, developed and published by YOSHITAKA MATSUSHIMA, has released its latest version, 1.1, on 2017-01-06. This app falls under the Education category on the Google Play Store and has achieved over 10 installs. It currently holds an overall rating of 5.0, based on 1 reviews.

Organic Chemistry APK available on this page is compatible with all Android devices that meet the required specifications (Android 2.3+). It can also be installed on PC and Mac using an Android emulator such as Bluestacks, LDPlayer, and others.

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App Details

Package name: appinventor.ai_yfd51885.OrganicChemistry_e

Updated: 8 years ago

Developer Name: YOSHITAKA MATSUSHIMA

Category: Education

Installation Instructions

This article outlines two straightforward methods for installing Organic Chemistry on PC Windows and Mac.

Using BlueStacks

  1. Download the APK/XAPK file from this page.
  2. Install BlueStacks by visiting http://bluestacks.com.
  3. Open the APK/XAPK file by double-clicking it. This action will launch BlueStacks and begin the application's installation. If the APK file does not automatically open with BlueStacks, right-click on it and select 'Open with...', then navigate to BlueStacks. Alternatively, you can drag-and-drop the APK file onto the BlueStacks home screen.
  4. Wait a few seconds for the installation to complete. Once done, the installed app will appear on the BlueStacks home screen. Click its icon to start using the application.

Using LDPlayer

  1. Download and install LDPlayer from https://www.ldplayer.net.
  2. Drag the APK/XAPK file directly into LDPlayer.

If you have any questions, please don't hesitate to contact us.

Previous Versions

Organic Chemistry 1.1
2017-01-06 / 1 MB / Android 2.3+

About this app

Organic Chemistry (Basic Reaction Mechanism) is a useful App for learning the Basic Reaction Mechanism in organic chemistry by using curved arrows. Mastering the fundamentals of reaction mechanisms is an important survival skill for students learning organic chemistry.
Table of Contents (Total 106 videos)
1. Types of arrows used in organic chemistry
2. Basic principles in organic chemistry
3. Resonance
4. Halogenation of alkanes (Radical reaction)
5. Alkene addition reactions: Electrophilic additions 5-1. Addition of hydrogen halide
5-2. Stability of carbocations
5-3. Supplementary: Rearrangement reaction
5-4. Acid catalyzed addition of water (Hydration)
5-4. Reaction mechanism (How to draw curved arrows)
5-5. Oxymercuration
5-6. Hydroboration
5-7. Addition of halogen (Halogenation): Bromination
5-8. Reaction with peroxyacid (peracid): Epoxidation 5-9. Reaction with osmium tetroxide: Dihydroxidation
5-10. Reaction with ozone: Ozonolysis
5-11. Reaction with hydrogen (Catalytic hydrogenation)
6. Alkyne addition reactions: Electrophilic addition 6-1. Addition of hydrogen halide
6-2. Addition of water
6-3. Addition of halogen (Bromination) 6-4. Addition of hydrogen: Half reduction
6-5. Supplementary: Birch reduction
7. Electrophilic aromatic substitution 7-1. Nitration
7-2. Bromination
7-3. Sulfonation: Sulfonation is reversible !
7-4. Friedel-Crafts reactions 7-4. (A) Friedel-Crafts alkylation
7-4. (B) Friedel-Crafts acylation
7-5. Summary of electrophilic aromatic substitution
7-6. Electrophilic substitution of benzene derivatives 7-6-1. Reactivity
7-6-2. Orientation
7-7. Theory of orientation 7-7-1. Toluene: o,p-directing and activating
7-7-2. Phenol: o,p-directing and activating
7-7-3. Nitrobenzene: m-directing and deactivating
8. Nucleophilic substitution (SN2 and SN1) of alkyl halides 8-1. SN2 reaction
8-2. Reaction mechanism of SN2
8-3. SN1 reaction
8-4. Reaction mechanism of SN1
9. Elimination reaction (E2 and E1) of alkyl halides 9-1. E2 reaction
9-2. Reaction mechanism of E2
9-3. E1 reaction
9-4. Reaction mechanism of E1
10. Reaction of alcohols 10-1. Protonation with strong acids
10-2. Acid-catalyzed elimination of water (Dehydration)
10-3. Reaction with hydrogen halides
10-4. Reaction of allylic alcohols
10-5. Supplementary: Allyllic rearrangement
10-6. Supplementary: Saytzeff’s rule (Zaitsev’s rule)
11. Ethers: Synthesis and Reactions 11-1. Synthesis of ethers-1 11-2. Synthesis of ethers-2: Williamson Ether Synthesis
11-3. Acid cleavage of ethers: Reaction with acids
11-4. Supplementary: Removal of methyl protecting group
11-5. Nucleophilic opening of epoxides with Grignard reagents
12. Nucleophilic addition to carbonyl group (aldehydes and ketones) 12-1. The polarity of the C=O double bond
12-2. Nucleophilic addition to carbonyl group
12-3. Addition of alcohols: Hemiacetal and acetal formation
12-4. Addition of primary amines: Imine formation
12-5. Addition of Grignard reagents
12-6. Supplementary: Addition of Grignard reagents to carbon dioxide
12-7. Addition of acetylides
12-8. Addition of hydrogen cyanide
12-9. Reduction of ketones and aldehydes
13. Esters: Synthesis and Reactions 13-1. Synthetic method for esters-1: Fischer esterification
13-2. Synthetic method for esters-2: Methyl ester formation by diazomethane
13-3. Hydrolysis of esters
13-4. Supplementary: Acid-catalyzed hydrolysis of tert-butyl esters
13-5. Reaction with Grignard reagents
13-6. Reduction of esters
13-7. Alcoholysis of esters 13-8. Ammonolysis of esters
14. Enol and Enolate reactions (aldehydes and ketones) 14-1. Keto-enol equilibrium
14-2. Why are a-Hydrogens acidic ?
14-3. Enolization
14-4. Aldol reaction
14-5. Aldol condensation
14-6. E1cB reaction
15. Enolate reactions in esters 15-1. Claisen condensation
15-2. Dieckmann condensation and retro-Claisen condensation
15-3. Synthetic methods related to Claisen condensation
15-4. Acetoacetic ester synthesis
15-5. Malonic ester synthesis
16. Michael addition
17. Robinson annulation