Draw the missing product from the reaction below. OTs K* "OC(CH3)3 + K*¯OTS + HOC(CH3)3 draw structure ... What is the stereochemistry at any stereogenic centers in the product? The product is a racemic The product does not have a stereogenic mixture. center. The product retains the stereochemistry of the reactant. The product is an inversion of the stereochemistry of the reactant.
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.
![Draw the missing product from the reaction below.
OTs
K* "OC(CH)3
%23%3
+ K* ¯OTS + HOC(CH3)3
draw structure...
What is the stereochemistry at any stereogenic centers in the product?
The product does not have a stereogenic
The product is a racemic
mixture.
center.
The product retains the
stereochemistry of the reactant.
The product is an inversion of the
stereochemistry of the reactant.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fcfc726ac-887c-4d0e-8766-f0024c12ed63%2F2c0c69cb-5e76-4b93-adbb-eab5a2891480%2Fr5te8w_processed.jpeg&w=3840&q=75)
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