i See Periodic Table See Hint Add curved arrows to this enol structure to show the formation of the next intermediate.

Q: Question attached

A: Intramolecular reaction This reaction takes place within the same molecule. This reaction is…

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A: Nucleophile is a nucleus loving species. Water is a universal solvent.We have to find out when water…

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A: ch3 ch2 oh + Bf3 ch3 s ch3 + Alcl3 Ch3 co ch3 + Bf3 C6H11+ + H2O Br2 + FeBr3

Q: H ウー Liq. NH3 H. H H

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A: Preparation of 2,4-Dibromobenzoic acid from benzene can be done as follows:

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A: Dibenzaldehyde can be synthesized in aldol condensation reaction,In this reaction an enolate ion…

Q: Give detailed Solution with explanation needed    ...don't give Ai generated solution...don't give…

A: Step 1: The starting compound is isobutane (2-methylpropane), which has the structure:…

Q: :0:

A: Nucleophilic substitution reactions: these are the type of reactions in which nucleophile reacts…

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A: We have to carry out the given synthesis. The required synthesis is shown below

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A: Please note- As per our company guidelines we are supposed to answer only one question. Kindly…

Q: In Williamson ether synthesis reaction, NaH plays both roles as base and deprotonation to alcohol.…

A: Williamson synthesis is an old method of synthesis of ether , using Sn2 reaction mechanism :…

Q: Hofmann Elimination Reaction NH₂ Draw all missing reactants and/or products in the appropriate boxes…

A: Hoffmann elimination rule :

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Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A: Given : structure of reactant.

Q: draw the step one product and draw curved arrows to show the nucleophilic addition step.

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A: When an alcoxide ion reacts with alkyl halide it forms ether. This reaction is known as williamson…

Q: benzoic acid from benzamide equation (use curly arrows)

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A: The objective of this question is to show the reaction involves the esterification of methyl…

Q: Please explain in clear terms. I don't understand the sentences following "Now, if stronger will be…

A: See nucleophile means -vely charged spececies and it attack on electrophile means +vely charged…

Q: In this reaction, which is the leaving group? A) B) to E) None of the other options H Br C)

A: This reaction shows an elimination reaction . This is E2 elimination.

Q: Rank the following compounds in order of increasing reactivity [least CH3CONH2> CH3COCI > CH3COOC2H5…

A: Reaction in which a nucleophile displace leaving group of acyl derivatives like acid halide,amide…

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Q: Draw bith the higher molecular weight prlduct and the lowe weight product

A: This is a SN2  type reaction:

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Q: What is a primary alcohol converted into when it is reacted with Hypochlorous Acid?

A: Hypochlorous acid (HOCl) acts as an oxidizing agent when reacting with primary alcohols.

Q: groups and which of these functional groups will be more reactive to nucleophilic addition

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Q: _(4a)_ + NaHCO, H2O (4b)_

A: Benzoic acid react with sodiumbicarbonate gives sodiumbenzoate and carbondioxide and water.

Q: Please don't provide handwritten solution...

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Q: Synthesize attached compound from cyclohexanol using any other organicor inorganic compounds.

A: The reactant given is cyclohexanol.

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A: Lithium aluminum hydride is strong reducing agent. It reduces carboxylic acid to alcohol.

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A: Phenolics: Phenolic compounds are compounds that have one or more hydroxyl groups on the aromatic…

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Q: from and alcohol of two carbon or less Cl

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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.