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  1. 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, …

  2. 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 …

  3. 18.6: Reactions of Epoxides - Ring-opening - Chemistry LibreTexts

    Epoxides may be cleaved by hydrolysis to give trans-1,2-diols (1,2 diols are also called vicinal diols or vicinal glycols). The reaction can be preformed under acidic or basic conditions which will …

  4. 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 …

  5. Epoxides - The Outlier Of The Ether Family – Master Organic ...

    2015年1月26日 · Properties and Synthesis of Epoxides. Epoxides (oxiranes) are cyclic ethers that have unusually high reactivity due to ring strain (about 25 kcal/mol). The 3-membered ring of …

  6. Epoxide Functional Group - ChemTalk

    What is an epoxide? An epoxide is a unique functional group found in many organic compounds. The group involves two carbons and oxygen forming a three-membered ring structure. Due to …

  7. Epoxide: Structure, Formation, Reactions & Uses

    Explore epoxides (oxiranes): their unique three-membered ring structure, synthesis methods like peracid epoxidation, and diverse reactions. Learn about real-world examples like ethylene oxide …