Q1: Device a synthesis of the following compound from cyclopentanone, benzene, and organic alcohols having ≤ 3 C's. you may also use any required organic or inorganic reagents. HO C6H5

Q: Bonus: 0-0-0-0

A: Approach to solving the question:  Detailed explanation: Examples: Key references:

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Q: Please help me with this, double check your answers other tutors got it wrong.

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A: In the reaction between an alcohol i.e ROH and HX, the below steps takes place. (The reaction…

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Q: Cesium Chromate + strontium phosphate -->

A: Cesium Chromate is Cs2CrO4 strontium phosphate is Sr3(PO4)2

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A: Balanced the given redox reaction under acidic solution---

Q: HBr `OCH3

A: The answer of following guestion is given below.

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Q: Write Kep for Ca3(POg)2 salt ..

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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.