Epoxide - Wikipedia
In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen. This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers. They are produced on a large scale for many applications.
Epoxide Functional Group - ChemTalk
In this organic chemistry tutorial, we learn about the epoxide functional group, including its definition, basic properties, naming conventions, and important reactions.
9.6. Epoxide reactions | Organic Chemistry 1: An open textbook
Epoxides (also known as oxiranes) are three-membered ring structures in which one of the vertices is an oxygen and the other two are carbons. The carbons in an epoxide group are very reactive electrophiles, due in large part to the fact that substantial ring strain is relieved when the ring opens upon nucleophilic attack.
18.6: Reactions of Epoxides - Ring-opening - Chemistry LibreTexts
write an equation to illustrate the cleavage of an epoxide ring by a base. identify the product formed from the reaction of a given epoxide with given base. explain why epoxides are susceptible to cleavage by bases, whereas other cyclic ethers are not.
Epoxide | Synthesis, Reactions, Ring-Opening | Britannica
Epoxide, cyclic ether with a three-membered ring. The basic structure of an epoxide contains an oxygen atom attached to two adjacent carbon atoms of a hydrocarbon. The strain of the three-membered ring makes an epoxide much more reactive …
3.9: Ethers, Epoxides and Sulfides - Chemistry LibreTexts
Simple epoxides are named from the parent compound ethylene oxide or oxirane, such as in chloromethyloxirane. As a functional group, epoxides feature the epoxy prefix, such as in the compound 1,2-epoxycycloheptane , which can also be called cycloheptene epoxide , or simply cycloheptene oxide .
9.6: Epoxide reactions - Chemistry LibreTexts
Epoxides (also known as oxiranes) are three-membered ring structures in which one of the vertices is an oxygen and the other two are carbons. The carbons in an epoxide group are very reactive electrophiles, due in large part to the fact that substantial ring strain is relieved when the ring opens upon nucleophilic attack.
Epoxides - The Outlier Of The Ether Family - Master Organic Chemistry
Jan 26, 2015 · Epoxides (“Oxiranes”) Are An Unusually Reactive Type of Cyclic Ether. If you think of ethers as a generally staid, stable, and placid family of functional groups, epoxides are definitely the outlier.
18.4 Cyclic Ethers: Epoxides - Organic Chemistry - OpenStax
The one group of cyclic ethers that behaves differently from open-chain ethers are the three-membered-ring compounds called epoxides, or oxiranes, which we saw in Section 8.7. The strain of the three-membered ring gives epoxides unique chemical reactivity.
Epoxy - Wikipedia
Epoxy resins, also known as polyepoxides, are a class of reactive prepolymers and polymers which contain epoxide groups. The epoxide functional group is also collectively called epoxy. [1] The IUPAC name for an epoxide group is an oxirane.