Difference between revisions of "Ether"
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*Cyclic ethers: [[Tetrahydrofuran]], [[1,4-Dioxane]], 2-methyltetrahydrofuran | *Cyclic ethers: [[Tetrahydrofuran]], [[1,4-Dioxane]], 2-methyltetrahydrofuran | ||
| − | One of the most known characteristics of | + | One of the most known characteristics of ethers is their tendency to form explosive peroxides when stored for long periods of time in contact with air or oxygen. The reaction is accelerated by light, metal catalysts, and aldehydes. Ethers like dimethyl ether or methyl tert-butyl ether however, do not form peroxides. |
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| + | ==References== | ||
| + | </references> | ||
| + | ===Relevant Sciencemadness threads=== | ||
| + | *[http://www.sciencemadness.org/talk/viewthread.php?tid=12288 ether peroxides] | ||
[[Category:Chemical compounds]] | [[Category:Chemical compounds]] | ||
Revision as of 10:25, 10 July 2016
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Ethers are a class of organic compounds, where two alkyl or aryl groups are connected to an oxygen atom. The general formula for an ether is R–O–R for simple or symmetrical ethers or R–O–R' for mixed or unsymmetrical ethers.
Examples of ethers:
- Symmetrical ethers: Diethyl ether, diisopropyl ether
- Unsymmetrical ethers: Methyl tert-butyl ether
- Cyclic ethers: Tetrahydrofuran, 1,4-Dioxane, 2-methyltetrahydrofuran
One of the most known characteristics of ethers is their tendency to form explosive peroxides when stored for long periods of time in contact with air or oxygen. The reaction is accelerated by light, metal catalysts, and aldehydes. Ethers like dimethyl ether or methyl tert-butyl ether however, do not form peroxides.
References
</references>
