Write a detailed, stepwise mechanism for the following free-radical monochlorination. reaction. CH3 + Cl₂ - (CH₂)₂CHCH₂CH₂ + Brz Draw the major monobromination product in the following reactions, and name it by IUPAC rules. -CH₂Cl + HCI Methylcyclopentane + Brz

Q: Use the References to acce important valuen if needed for this question Does a reaction occur when…

A: This reaction will not occur.

Q: HCI

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A: Hello. Since the question contains more than three sub-parts, the first three sub-parts shall only…

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Q: My teacher marked option b) as a mistake.

A:

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A: Here is the answer

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A:

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A:

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A: It is the electron density surface of the molecule. In this molecules the red colour show the  more…

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.