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Organic Chemistry on Windows Pc

Developed By: YOSHITAKA MATSUSHIMA

License: Free

Rating: 5,0/5 - 1 votes

Last Updated: December 27, 2023

Download on Windows PC

Compatible with Windows 10/11 PC & Laptop

App Details

Version 1.1
Size 1 MB
Release Date January 06, 17
Category Education Apps

Description from Developer:
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 r... [read more]

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About this app

On this page you can download Organic Chemistry and install on Windows PC. Organic Chemistry is free Education app, developed by YOSHITAKA MATSUSHIMA. Latest version of Organic Chemistry is 1.1, was released on 2017-01-06 (updated on 2023-12-27). Estimated number of the downloads is more than 10. Overall rating of Organic Chemistry is 5,0. Generally most of the top apps on Android Store have rating of 4+. This app had been rated by 1 users, 1 users had rated it 5*, 1 users had rated it 1*.

How to install Organic Chemistry on Windows?

Instruction on how to install Organic Chemistry on Windows 10 Windows 11 PC & Laptop

In this post, I am going to show you how to install Organic Chemistry on Windows PC by using Android App Player such as BlueStacks, LDPlayer, Nox, KOPlayer, ...

Before you start, you will need to download the APK/XAPK installer file, you can find download button on top of this page. Save it to easy-to-find location.

[Note] You can also download older versions of this app on bottom of this page.

Below you will find a detailed step-by-step guide, but I want to give you a fast overview of how it works. All you need is an emulator that will emulate an Android device on your Windows PC and then you can install applications and use it - you see you're playing it on Android, but this runs not on a smartphone or tablet, it runs on a PC.

If this doesn't work on your PC, or you cannot install, comment here and we will help you!

  1. Install using BlueStacks
  2. Install using NoxPlayer

Step By Step Guide To Install Organic Chemistry using BlueStacks

  1. Download and Install BlueStacks at: https://www.bluestacks.com. The installation procedure is quite simple. After successful installation, open the Bluestacks emulator. It may take some time to load the Bluestacks app initially. Once it is opened, you should be able to see the Home screen of Bluestacks.
  2. Open the APK/XAPK file: Double-click the APK/XAPK file to launch BlueStacks and install the application. If your APK/XAPK file doesn't automatically open BlueStacks, right-click on it and select Open with... Browse to the BlueStacks. You can also drag-and-drop the APK/XAPK file onto the BlueStacks home screen
  3. Once installed, click "Organic Chemistry" icon on the home screen to start using, it'll work like a charm :D

[Note 1] For better performance and compatibility, choose BlueStacks 5 Nougat 64-bit read more

[Note 2] about Bluetooth: At the moment, support for Bluetooth is not available on BlueStacks. Hence, apps that require control of Bluetooth may not work on BlueStacks.

How to install Organic Chemistry on Windows PC using NoxPlayer

  1. Download & Install NoxPlayer at: https://www.bignox.com. The installation is easy to carry out.
  2. Drag the APK/XAPK file to the NoxPlayer interface and drop it to install
  3. The installation process will take place quickly. After successful installation, you can find "Organic Chemistry" on the home screen of NoxPlayer, just click to open it.

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Download older versions

Other versions available: 1.1.

Download Organic Chemistry 1.1 on Windows PC – 1 MB

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