Нитроэтилен википедия

Мы профессиональная команда, которая на рынке работает уже более 2 лет и специализируемся исключительно на лучших продуктах.

У нас лучший товар, который вы когда-либо пробовали!

Наши контакты:

Telegram:

https://t.me/happystuff

Внимание! Роскомнадзор заблокировал Telegram ! Как обойти блокировку:

http://telegra.ph/Kak-obojti-blokirovku-Telegram-04-03-2

ВНИМАНИЕ!!! В Телеграмм переходить только по ссылке, в поиске много фейков!

Nitroethylene also known as nitroethene is a liquid organic compound with the formula C 2 H 3 NO 2. It is the simplest nitroalkene , which are unsaturated carbon chains with at least one double bond and a NO 2 functional group. Nitroethylene serves as a useful intermediate in the production of various other chemicals. Nitroethylene has a dipole moment from the electron withdrawing nitro group present in the molecule, even though it is a neutral species. As a result, it is soluble in water and non-polar solvents. Nitroethylene is extremely reactive, even at low temperatures. It readily decomposes at room temperature. Nitroethene can be produced by reacting nitromethane with formaldehyde or paraformaldehyde a polymeric form to form 2-nitroethanol, which can then undergo an E2 acid-catylized dehydration reaction. Nitroethylene is a very electron deficient molecule. As a result, nitroethylene usually acts as the electrophile in reactions. Common reactions for this molecule are cycloadditions, radical additions, and nucleophilic additions. The nitro group in the molecule serves as an electron withdrawing group that makes the molecule a good candidate as a dienophile. Nitroethylene is also reactive in domino-cycloaddition processes. At very low temperatures i. This process can be moderated by using t-butyl solvent. Research has been conducted on performing batch polymerization at room temperature in THF solvent. This process requires gamma ray irradiation for initiation. Termination of the polymerization requires a radical retardant, such as hydrogen bromide or hydrogen chloride. Water must be carefully removed prior to the polymerization, as nitroethylene is sensitive to polymerization by traces of water. A typical Michael donor i. Another example is the Michael reaction of indole and nitroethylene. The main use of nitroethylene is as an intermediate reagent in chemical synthesis. One example is the production of N- 2-nitroethyl -aniline with aniline at room temperature. Another example of nitroethylene is from the coupling reaction with a vinyl Grignard and a silyl glyoxalate to form a nitrocylopentanol. This process via a Henry reaction and is highly diastereoselective. From Wikipedia, the free encyclopedia. This article needs more links to other articles to help integrate it into the encyclopedia. Please help improve this article by adding links that are relevant to the context within the existing text. May Learn how and when to remove this template message. Specific heat capacity C. Std molar entropy S o Radiation-Induced Polymerization of Nitroethylene. The Journal of Organic Chemistry. Chemistry of Heterocyclic Compounds. Collection of Czechoslovak Chemical Communications. Angewandte Chemie International Edition , , 49 47 , pp. Retrieved from ' https: Nitro compounds Alkene derivatives Vinyl compounds. Views Read Edit View history. This page was last edited on 6 September , at By using this site, you agree to the Terms of Use and Privacy Policy.

Купить МЁД Далматово

Нитроэтилен википедия

Синтез фенилнитропропена

Нитропропен

1 фенил 2 метил 2 нитроэтилен купить

Фенил метил нитроэтилен

Nitroethylene

1-Фенил-2-нитропропен

Все товары

Для чего применяется 2-фенил-нитропропен?

Синтез фенилнитропропена

Синтез фенилнитропропена

Report Page