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

Q: Draw the products of each Lewis acid-base reaction and label the electrophile and nucleophile. CH3…

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

A: The elimination-then-addition reaction of an aromatic compound involves two steps: elimination of a…

Q: Show all the steps necessay,in order to make each of the followring compoundS, Starting with benzene…

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

Q: Both compounds A and B below give the same carbocation intermediate C in the SN1 reaction. However,…

A: In this question, we will Identify which Compound ( A or B ) give carbocation intermediate ( C )…

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…

Q: х бон

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

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 :

Q: Is the following true or false? When you consider the normal polarity of a carbonyl molecule it…

A:

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.

A: To provide the arrow mechanism for the first step of the Fischer esterification reaction and the…

Q: Illustrate Williamson synthesis by giving chemical reaction   Plz only give in five sentences only…

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)

A: The objective of the question is to understand the mechanism of conversion of benzamide to benzoic…

Q: Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a…

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: Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and…

A:

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

A: This is a SN2  type reaction:

Q: 2. For each pair of structures below... i. ii. iii. Circle the structure that is more likely to be…

A: Firstly we must know about the nucleophile?  What is nucleophile?  Nucleophile is an electron rich…

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

A: Four compounds are given, in which different types of functional groups present. From them we chose…

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

A: Some general rules to follow when drawing arrow pushing mechanisms:Arrows Represent Electron…

Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows to predict the…

A: When an ether reacts with HCl, an alcohol and an alkyl chloride will be formed.

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

A: The reactant given is cyclohexanol.

Q: Draw a mechanism for the reduction of the carboxylic acid with lithium aluminum hydride (LAH).…

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

Q: When the depicted alkyne is treated first with sodium amide and then with the alkyl halide shown,…

A: We have given when  alkyne is treated first with sodium amide and then with the alkyl halide. It is…

Q: Consider molecules A–D. Does the arrow pushing in each structure lead to an acceptable resonance…

A:

Q: The Friedel-Crafts alkylation reaction how it works it helpf to form new carbon bonds and adds alkyl…

A: A question based on Friedel-Craft alkylation reaction, which is to be accomplished.

Q: from and alcohol of two carbon or less Cl

A:

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.