Скачать Organica-II 1.0 на ПК с помощью эмулятора GameLoop

Organica-II 1.0 на ПК

Organica-II 1.0, исходящий от разработчика Arun Kumar Gupta, в прошлом работал на системе Android.

Теперь вы можете без проблем играть в Organica-II 1.0 на ПК с помощью GameLoop.

Загрузите его в библиотеке GameLoop или результатах поиска. Больше не нужно смотреть на аккумулятор или разочаровывать звонки в неподходящее время.

Просто наслаждайтесь Organica-II 1.0 на ПК на большом экране бесплатно！

Organica-II 1.0 Введение

In this app we will learn, how we carried out the Pharmaceutical Organic Chemistry practical in laboratory with safety. This app also give general information about safety and precautions, laboratory glassware’s and equipment’s with pictorial representation. This application guides the students to perform the Organic chemistry (pharmaceutical organic chemistry-II) practical in a simple and easy manner.

All the experiments commonly performed especially by the Pharmacy students as wells as Chemistry graduates. HandyLabs Organica-II includes preparation, analysis of oils/fats and laboratory techniques of organic chemistry. Each experiment contains Object, Principle, Procedure Observation and Result in a very illustrative manner. Each part of the experiment are clearly explain with diagram. The speciality of the application is demonstration video included for easy understanding of learners.

This app version 1.0 certainly based on the response it will be converted in more practical aspect with user friendly.

Experiments involving laboratory techniques

• Recrystallization

• Steam distillation

II Determination of following oil values (including standardization of reagents)

• Acid value

• Saponification value

• Iodine value

III Preparation of compounds

• Benzanilide from Aniline by acylation reaction.

• Phenyl benzoate Phenol by acylation reaction.

• Acetanilide from Aniline by acylation reaction.

• 2,4,6-Tribromo aniline from Aniline by halogenation (Bromination) reaction.

• Para bromo acetanilide from Acetanilide by halogenation (Bromination) reaction.

• 5-Nitro salicylic acid from Salicylic acid by nitration reaction.

• Meta di nitro benzene from Nitro benzene by nitration reaction.

• Benzoic acid from Benzyl chloride by oxidation reaction.

• Benzoic acid from alkyl benzoate by hydrolysis reaction.

• Salicylic acid from alkyl salicylate by hydrolysis reaction.

• 1-Phenyl azo-2-napthol from Aniline by diazotization and coupling reactions.

• Benzil from Benzoin by oxidation reaction.

• Dibenzal acetone from Benzaldehyde by Claison Schmidt reaction

• Cinnammic acid from Benzaldehyde by Perkin reaction

• P-Iodo benzoic acid from P-amino benzoic acid