(f) This part of the question refers to the substituted alcohol (N) given below. CH3 Br N (i) Classify N as a primary, secondary, tertiary or quaternary halide. (ii) Based on this classification, which reaction mechanism (SN1 or SN2) would you expect N to undergo faster? Why?

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A:

Q: CN .CN NH3 CH3OH Br Br `NH2

A:

Q: Propose a reasonable mechanism that would account for the reaction shown here. H2O HBr НО

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A: A question based on reaction mechanism and stereochemistry, which is to be accomplished.

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A: Trichloroethanol may be prepared by the direct reduction of chloral hydrate in water with sodium…

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A:

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Q: reaction or conditions in each pair that you expect will react FASTER for the mechanism provided.…

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A:

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Q: Which of the following reacts fastest with methanol by the SN1 mechanism?

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Q: 6

A: First mercuration of alkene will happen.

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Q: Provide a reasonable mechanism that provides the major product for the reaction scheme provided…

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Q: HO: What is wrong with the mechanism described below?

A:

Q: Which of the reactants in the picture will undergo the fastest SN1 reaction in ethanol? O D

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Q: b. Write the reaction mechanism for each using the right arrows and define it as Sn2, Sn1, E2 or E1.

A:

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A: Given reaction,

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A:

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A: The details solution for this reaction is provided below in attach image.

Q: Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane…

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A:

Q: Complete the following reactions, write major product(s) and specify the mechanism if ; SN1, SN2, E,…

A: We will write the product

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Q: 3. Give the mechanism, using the arrow notation, for each of the reactions below.

A:

Q: 2) Rank these molecules by their SN2 reaction rate. If a difference in reaction rate is hard to…

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Q: CH3 CH2BR NBS hv

A:

Q: Give 3 examples of a reaction mechanism of E1 that follows Zaitsev's rule.

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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.