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.
Mechanism to all parts?
![3) Predict the products of the following reactions:
a)
b)
c)
lã
Br
Mg
Ether
Mg
Ether
(N)
H₂O
1. 2x (N) from above
2. H₂O+
MgBr
Reading Through PP10 From Jan 27th and the textbook Ch 10 and Ch 14, give an explanation using
both diagrams and words for why alcohols tend to have higher boiling points than ethers.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1ef05a66-795b-406c-abf3-738695280729%2Ff800ec39-1eb9-46d6-85da-785cda87d79d%2Fv5fnzxn_processed.jpeg&w=3840&q=75)
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