2. The following transformation takes place when a strong base such as methoxide is used. Please propose a reasonable mechanism for this reaction. животни и два La + H₂ CO₂Me H MeO₂C Ome MeO₂C MeO₂C CO₂Me CO₂Me

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A: This is E1 reaction i.e unimolecular elimination reaction.In this reaction, alkyl halide is…

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A:

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A:

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A:

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A: Given reaction,

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A:

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A:

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A:

Q: using the starting materials given below. Any reagent needed can be used and you may need more than…

A: Applying concept of organic synthesis and reagent.

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A:

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Q: 9. Mechanism: Propose a mechanism for the following transformation. Br L Br H₂O

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Q: b. HO,

A: The following compounds can be synthesized by the following reactions:

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.