epoxide | Epoxide - Wikipedia

Keyword	CPC	PCC	Volume	Score	Length of keyword
epoxide	1.71	1	3628	6	7

Keyword	CPC	PCC	Volume	Score
epoxide	1.97	0.9	2821	75
epoxide ring opening	1.5	0.5	1115	52
epoxide formation	1.23	0.2	4394	20
epoxide resin	1.66	0.5	1229	70
epoxide reactions	0.47	0.4	1910	62
epoxide hydrolase	1.89	0.9	4590	51
epoxide group	1.74	0.9	9503	16
epoxide ring	1.07	0.5	6352	28
epoxide opening	1.3	0.2	3208	85
epoxide structure	1.08	0.1	8439	91
epoxide reductase	0.13	0.6	5106	80
epoxide meaning	0.36	0.1	2708	93
epoxide functional group	1.8	0.8	1707	82
epoxide mechanism	0.81	0.5	8030	61
epoxide ring opening mechanism	1.14	0.7	7763	38
epoxide hydrolysis	1.37	0.9	4649	31
epoxide formation mechanism	0.46	0.2	1728	62

Search Results related to epoxide on Search Engine

Epoxide - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Epoxide

WebIn 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.

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18.6: Reactions of Epoxides - Ring-opening - Chemistry LibreTexts
libretexts.org

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/18%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/18.06%3A_Reactions_of_Epoxides_-_Ring-opening

WebUnder aqueous basic conditions the epoxide is opened by the attack of hydroxide nucleophile during an S N 2 reaction. The epoxide oxygen forms an alkoxide which is subsequently protonated by water forming the 1,2-diol product. If the epoxide is asymmetric the incoming hydroxide nucleophile will preferable attack the less substituted epoxide …

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Epoxide | Synthesis, Reactions, Ring-Opening | Britannica
britannica.com

https://www.britannica.com/science/epoxide

WebEpoxide, 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 than a typical acyclic ether. Ethylene oxide is economically.

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15.7: Synthesis of Epoxides - Chemistry LibreTexts
libretexts.org

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Wade)_Complete_and_Semesters_I_and_II/Map%3A_Organic_Chemistry_(Wade)/15%3A_Ethers_Epoxides_and_Thioethers/15.07%3A_Synthesis_of_Epoxides

WebEpoxides (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 most important and simplest epoxide is ethylene oxide which is prepared on an …

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18.6 Reactions of Epoxides: Ring-opening - Chemistry LibreTexts
libretexts.org

https://chem.libretexts.org/Courses/Athabasca_University/Chemistry_360%3A_Organic_Chemistry_II/Chapter_18%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/18.06_Reactions_of_Epoxides%3A_Ring-opening

WebNov 16, 2023 · Ring-opening reactions can proceed by either S N 2 or S N 1 mechanisms, depending on the nature of the epoxide and on the reaction conditions. If the epoxide is asymmetric, the structure of the product will vary according to which mechanism dominates.

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Epoxy - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Epoxy

WebEpoxy 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 .

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18.4 Cyclic Ethers: Epoxides - Organic Chemistry | OpenStax
openstax.org

https://openstax.org/books/organic-chemistry/pages/18-4-cyclic-ethers-epoxides

WebEthylene oxide, the simplest epoxide, is an intermediate in the manufacture of both ethylene glycol, used for automobile antifreeze, and polyester polymers. Approximately 37 million tons of ethylene oxide is produced worldwide each year, most of it by air oxidation of ethylene over a silver oxide catalyst at 300 °C.

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9.6. Epoxide reactions | Organic Chemistry 1: An open textbook
lumenlearning.com

https://courses.lumenlearning.com/suny-potsdam-organicchemistry/chapter/9-6-epoxide-reactions/

WebEpoxide ring-opening reactions – S N 1 vs. S N 2, regioselectivity, and stereoselectivity. The nonenzymatic ring-opening reactions of epoxides provide a nice overview of many of the concepts we have seen already in this chapter. Ring-opening reactions can proceed by either S N 2 or S N 1 mechanisms, depending on the nature of the epoxide and ...

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Epoxide - an overview | ScienceDirect Topics
sciencedirect.com

https://www.sciencedirect.com/topics/chemistry/epoxide

WebEpoxide. Also called epoxide, is an organic compound containing a three-membered ring involving an oxygen atom and two carbon atoms. From: Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, 2018

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The Outlier Of The Ether Family - Master Organic Chemistry
masterorganicchemistry.com

https://www.masterorganicchemistry.com/2015/01/26/epoxides-the-outlier-of-the-ether-family/

WebJan 26, 2015 · Last updated: November 7th, 2022 |. Properties and Synthesis of Epoxides. Epoxides (oxiranes) are cyclic ethers that have unusually high reactivity due to ring strain (about 13 kcal/mol). The 3-membered ring of epoxides can be opened under both acidic and basic conditions.

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