Draw the structure of the product that is formed when the compound shown below is treated with cold, diluted KMNO4, HO". Be sure to indicate stereochemistry if required. Interactive 3D display mode H,C. CH3
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.
Can you assist me in identifying the error in my drawing? Is the stereochemistry correct? Any feedback will be greatly appreciated. Thank you.
Question:
Draw the structure of the product that is formed when the compound shown below is treated with cold, dilute KMnO4, HO-. Be sure to indicate stereochemistry if required.
![Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
H: 120 EXP. CONT.
H
+
N
CH3
HOll
CI
Br
(1]
ČH3
F
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Please specify the configuration at both stereocenters.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb041252e-6a65-4a9d-bb85-93f64c65df81%2F634c1401-e511-4c60-abb1-78d8a02982c1%2Fc5ag35a_processed.png&w=3840&q=75)
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