Question

How do you name epoxides and ethers?

Answer 1

Hint:In order to name epoxides and ethers firstly the classify the compounds, a compound in which two carbon atoms are connected to an oxygen atom likewise epoxides are the three membered, cyclic compounds. Also all ethers will also have a similar common name, which is often used as with the IUPAC name. If we want to acquire the common name, we have to name the two groups flanking the $O$ atom in an alphabetized form and the word "ether" is added along with that.

Complete answer:
There are several ways of naming epoxides and ethers. In which epoxides is classified by two ways naming:
Substitutive names:These compounds we named as an alkane with an alkoxy alkane. Example $${\left(C{H}_3\right)}_{2}CH-O-C{H}_3$$ is $$2-methoxypropane$$
Functional class names:$$R-O-R^{\prime }$$ is named with the names of $R$ and $$R^{\prime }$$ in alphabetical order, followed by the class name "ether". Example $${\left(C{H}_3\right)}_{2}CH-O-C{H}_3$$ is ethyl isopropyl ether.
Also ethers is naming classified by-
Substitutive names:The compound is named as an alkene with an epoxy substituent. Example, $$1,2-epoxybutane$$

Functional class names:The compound is named as an epoxide of the corresponding alkene. Example, $$1,2-epoxybutane$$ is also named as $$but-1-eneepoxide$$
The Hantzsch Widman name:Here the ring we had named as a cyclopropane in which the $O$ atom replaces a $C{H}_2$ group indicated by the prefix "oxa" with the "a" which is being dropped when followed by a vowel. The three membered saturated ring is indicated by the prefix "ir" followed by the suffix "ane".
Therefore, $$1,2-epoxybutane$$ is called ethyloxirane. The O atom is automatically number $1$ , so the ethyl group is on $C-2$ . We have no locating number is necessary here, because there is no such compound as $$3-ethyloxirane$$
Oxide of the Correspondent alkene:Examples are ethylene oxide and propylene oxide. The first three methods are accepted by IUPAC.
The fourth is used only for simple alkenes such as ethylene, propylene, and butylene.

Note:Also note that thiols are compounds that are structurally identical to alcohols except that they replace the oxygen atom in the hydroxyl group with a sulfur atom. Likewise, sulfides are structurally identical to ethers, but they replace the oxygen atom with a sulfur atom, as shown below.