The following reaction takes place several times faster than the reaction of 2-chlorobutane with HO-: (CH3CH2)2N CH2CHCH2CH3Cl (CH3CH2)2N CHCH2CH3CH2OH

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Q: 1. Predict the major product(s) from the treatment of acetone with the following compounds: (a)…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: a stepwise mechanism for the conversion of 2,6-heptanedione to 3-methyl-2-cyclohexenone with NaOEt,…

A: The stepwise mechanism for the conversion of 2,6-heptanedione to 3-methyl-2-cyclohexenone with…

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A: Acetate Ion will de-protonate the phenol to form phenoxide ion as follows,

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A: The given intramolecular bromoetherification reaction is as follows,

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Q: Draw all of the expected products from the following reaction: (2 equiv.)

A: An acid anhydride reacts with amine to form an amide.

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A: Alcoholic hydrolysis of ester using sulfuric acid as catalyst

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A: The compounds given are,

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Q: 5. 6 HO. + (in excess; used as solvent) 3 2

A: E2 elimination reaction

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Q: Which reagents would afford the product shown? 1 2 HO. NBS, heat; 2. Na2Cr2O7, H2SO4(aq) 1. KMNO4,…

A: NBS - It stands for N-bromo succinimide. It is a brominating agent. It releases Bromine radical on…

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A: The reaction os simple conjugate addition to unsaturated carbonyl compound.

Q: m. SN1 SN2 E1 E2 CH;CH2CH2CH2-OH + POCI3 with pyridine → Product(s) of reaction m.

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Give the major elimination product of the following compoune ? (CH3)3COK heat CH3

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: (e) Provide a reasonable mechanism of the following reaction .CI OCH3 CH3ONA Ether (5) (c) Show how…

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A: Applying concept of reagents and reaction.

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A: product X of the following SN2 reaction is given as

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A: The compound C formed in the reaction is shown below.

Q: CI I II IV

A: The correct answer is given below

Q: CH3CH2OH Br

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A: Given reaction,

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A: Concept is based on Nitration.

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A: Concept is based on aromatic electrophilic substitution reactions.

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A: To describe the mechanisms of the products(A and B) formed:

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A: Organic Transformation for Cyanide group to Primary Amine

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Q: 5) Which one of the following compound can react faster with concentrated H2SO4 under reflux(heat)?…

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A: The compound C formed in the reaction is shown below.

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A:

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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.