The following reaction resembles the acid-catalyzed cyclization of squalene oxide. Propose a mechanism for this reaction.

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A:

Q: Practicce chemistry question

A: silicon dioxide generally Known as silicate not easily reactive with acids in normal conditions but ...

Q: Give the IUPAC name for attached compound.

A: IUPAC name of the compound is given by identifying the functional group and the parent name.

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A: So, we are provided with 1000 ppm each of Cu, Mn, K, Na and Ca.

Q: 2 please! It got rejected, so please send me my amount of questions back!☺️

A: NOTE ; Since you've posted multiple questions,we'll solve only first question for you. If you want a...

Q: Show how the following compound can be prepared from benzene:

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A:

Q: Please convert the problem three the flowing into moles to representative particles

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A: Tetrahedral.

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Q: Multiply 21.5 x 3.149 and report the answer to correct sigfigs. 67.704 6.83 67.7 0 67 70

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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.