Click the "draw structure" button to launch the drawing utility. Compounds containing triple bonds are also Diels-Alder dienophiles. With this in mind, draw the product of the following reaction. draw structure ... 2+1 = CH3O OCH3

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Q: 14. State the ratio of atoms in one molecule of each of the following: a. stearic acid, C18H3602 b.…

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Q: The following chemical equations shows the stepwise Formation Constant expression (K₁ toks) of each…

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Q: Of these two products, which ionic compound is insoluble in water? O AgCl O NaNO3 10 60 5

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Q: d-) H₂CCCC₂H 1) 0₂ 2) Zn/H.O С

A: Ozonolysis of alkyne will occur.

Q: recrystallisation

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A:

Q: HC HO CH CH C1 h Chemical formula: C1

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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.