E Module 13 HW Chapter 21 - Selected Exercises Question 2 of 9 < > -/1 E Identify the reagents you would use to convert cyclohexanone into the following compound: 1)? 2) ? 3)? Choose from the following list of reagents: A C D Mel LIAIH4 LDA NaOEt/EtOH G H. NAOH H3O* Et2Culi R2NH [H*], (-H2O) H20, heat w
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.
![e Module 13 HW Chapter 21 - Selected Exercises
Question 2 of 9
<>
-/1 E
Identify the reagents you would use to convert cyclohexanone into the following compound:
1)?
2) ?
3)?
Choose from the following list of reagents:
A
Mel
LIAIH4
LDA
NaOEt / ETOH
F
G
H
R2NH
[H*], (-H2O)
NAOH
Et2CuLi
H20, heat
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4)
F1
F12
F9
F10
F8
F6
F7
F5
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7
8.
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![uestion 2 of 9
NaOn
H20, heat
[H*], (-H2O)
COET
Reagent 1:
Reagent 2:
Reagent 3:
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F10](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F495b7754-d09d-4802-adb5-6dc5cbab558a%2Faf8c0557-28d0-4046-927a-c8395957d1d3%2F5ijxfg0h_processed.jpeg&w=3840&q=75)
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