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An epoxide is characterized specifically by its three-membered ring structure that incorporates one oxygen atom and two carbon atoms. This unique configuration leads to significant ring strain, making epoxides quite reactive compared to larger cyclic ethers. The three-membered nature of the ring means that the angle between the carbons and the oxygen is much smaller than the typical bond angles in open-chain alkanes or larger rings, creating inherent instability.

In addition to the three-membered ring feature, while epoxides may interact with nucleophiles and exhibit reactivity due to ring strain, this reactivity is a consequence of the structural characteristics rather than a defining feature. Thus, the specificity of the three-membered oxygen-containing ring is what primarily defines an epoxide.

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