Sulfonation of benzene is a reversible reaction. Using the principal of microscopic reversibility, propose a complete mechanism for the removal of the sulfonate group from benzenesulfonic acid.

Q: 2.

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Q: 2.

A: Reaction 1 : Esterification followed by C-acylation. Reaction 2 : C- acylation followed by Michael…

Q: In the acid-catalyzed dehydration of 2-methyl-1-propanol, what carbocation would be formed if a…

A: The hydrocarbons which contain all single covalent bonds with the general formula Cn H2n+2 are…

Q: Chlorocatechelin A was isolated from a bacterial culture, but it had to be synthesized in the…

A: Given :  To propose a plausible mechanism for a reaction starting from ortho-vanillin.

Q: Provide the full mechanism for nitration of benzene. Show how the electrophile is formed and how the…

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Q: c) When compound A is treated with the strong base lithium diisopropylamine (LDA) followed by an…

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Q: Strong support for the mechanism of the nucleophilic aromatic substitutionreaction that proceeds…

A: Bromobenzene will react with KNH2 to give the benzyne intermediate which will further react with the…

Q: Write a mechanism for the following reaction

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

Q: 4. Give a detailed mechanism for a reaction of ethylamine and acetyl chloride under basic…

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Q: Propose a reasonable synthetic route for the following conversion. Show all isolated intermediates.

A: Answer is given in below image

Q: Acid-catalyzed transesterification and Fischer esterification take place by nearly identical…

A: Concept introduction: Transesterification involves the interchange of alkoxy groups when ester is…

Q: A student in Ochem proposed the following synthesis. Explain the problem with this approach and…

A: LDA ( lithium diisopropylamide) is a larger base .Thus it accepts the it accepts protons from less…

Q: Write the detailed mechanisms for the following transformations.

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Q: Outline a detailed mechanism for the problem below. No other reagents other than those given are…

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Q: Using the disconnection approach propose a reasonable retrosynthetic route to accomplish the…

A: The retrosynthetic analysis for the compound:

Q: Bringing together your knowledge of the reaction chemistry of substituted benzenes, suggest a…

A: Convertion of A to B can be done in two steps. They are,

Q: Provide the structure of the hydrate of cyclopentanone.   b. Provide the major organic product…

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Q: Enamines can react with acyl chlorides via nucleophilic addition-elimination, such as in the…

A: A 1,3-diketone has been obtained via nucleophilic addition-elimination reaction between the enamine…

Q: Depict a competent mechanism for the formation of DEET using m-toluic acid and oxalyl chloride, with…

A: Synthesis of DEET using m-toluic acid, oxalyl chloride and diethylamine, whose mechanism is to be…

Q: Write a detailed mechanism for this transformation. OH HCI НО НО H2O -OH

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Q: 1. Describe how the compound A could be prepared from benzene. Write the mechanism of this reaction.…

A: Organic reactions are those in which organic compounds  react with each other. For example:…

Q: CH

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Q: Write the overall balanced equation for the transformation of bromobenzene into benzoic acid through…

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Q: For each of the following transformations, propose a realistic synthesis:

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Q: Define the General Mechanism–Acid-Catalyzed Nucleophilic Addition ?

A: A nucleophilic expansion response is a compound expansion response where a nucleophile structures a…

Q: Account for complete retention of configuration in the solvolysis of (1).

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Q: Define the Mechanism - Conversion of Acid Chlorides to CarboxylicAcids ?

A: Acid chlorides: Also known as Acyl chloride is one of the derivatives of acid in which OH group is…

Q: provide the (S) configuration reaction mechanism for the synthesis of camphor from isoborneol

A: camphor:  .  It is a terpenoid .  Molecular formula C10 H16O  Oxidation of isoborneol in presence of…

Q: Write a detailed mechanism for the following reaction. KCN. HCN

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Q: Propose a multi-step synthesis for converting 1-methylcyclohexene to racemic 6-hydroxyheptanoic acid…

A: The mechanism of this reaction is hereby attached .

Q: Outline a mechanism for the following reaction: CH3 CH3 CH3 CH3 NaNH2 NH2 NH3, 350°C `NH2 NH2

A: Mechanism of the reaction.

Q: 5. Optically pure 2-octyl sulfonate was treated with varying mixtures of water and dioxane, and the…

A: SN2 reaction proceeds through inversion in configuration Dioxane acts as a nucleophile. It reacts…

Q: Ph H₂SO4 Ph SO₂H Producto minoritario SO₂H Producto mayoritario

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Q: Synthesize the following ether from any two alcohols. YOU MUST SHOW the complete retrosynthetic…

A: synthesis of ether from alkylhalide and alkoxide ion is aceed williamson etherification   To do…

Q: Propose a mechanism for the acid-catalyzed hydration of propene. Remember that a mechanism must…

A: Alkene reacts with water in presence of acid to produce alcohol.

Q: 4. Provide a reasonable retrosynthetic route that involves a diazonium salt intermediate to…

A: First we can write the synthesis steps from starting material to get target molecule. The given…

Q: Esters can undergo hydrolysis to give an alcohol and a carboxylic acid. Lactone P which is a cyclic…

A: b) ester hydrolysis produces alcohol and carboxylic acid. Lactones hydrolysis produces a hydroxy…

Q: The following molecule is susceptible to nucleophilic attack at the carbonyl carbon as well as the B…

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Q: Complete the following reaction and provide a detailed, step-by-step mechanism for the process. !…

A: Hydration of alkene: Alkene gives hydration reactions in presence of an acid catalyst. In this…

Q: Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur…

A: Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur…

Q: Suggest a synthetic equivalent for each of the following synthons: (i) [ArCO]+, (ii) [ArCO]-, (iii)…

A: Note: According to our guidelines we are supposed to answer only first three subpart.  Kindly repost…

Q: Outline the mechanism of the reaction of 2 propanone with Ethanol/H+ showing the product/s that…

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Q: The following sequence of reactions features the Wolff-Kishner reduction - a reaction that converts…

A: The aromatic compound gives aromatic electrophilic substitution reactions. The aromatic compound can…

Q: Propose a plausible mechanism for each of the following transformations.

A: A detailed mechanism explained for first three reactions are given below