Reactions of Ethers
Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.
Epoxides
Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.
Williamson Ether Synthesis
An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.
Name the following skeletal structures
![The image depicts the structural formula of an organic compound, specifically a hydrocarbon. The molecule is represented with lines indicating bonds between atoms. In this structure:
- There is a main carbon chain consisting of five carbon atoms.
- Attached to the second carbon in the chain is a methyl group (CH₃).
- Chemical groups shown in the diagram are CH₃, indicating that these positions are occupied by methyl groups.
- This type of diagram is often used to represent the molecular structure of organic compounds, highlighting the arrangement of carbon and hydrogen atoms.
The number "5" and the letter "A" below the structure might indicate a label or reference for this compound in a set of similar diagrams or exercises.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F872b6c9e-2fcf-4b9e-96ef-3fd5bb9956d7%2Feb6288ed-bb4f-412b-bed2-1bb6202b9d5f%2Fyzw4owd_processed.png&w=3840&q=75)
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