3. The following reactions do not work well to produce the given substitution product. Explain why, and if something can be done to make the reaction work, offer a change.

Q: synthesising this molecule with the given reactant

A:

Q: 1. For the transformation below, provide a detailed arrow-pushing mechanism. If intermediates occur…

A: The given substrate to you, has a acidic hydrogen and a good leaving group -OEt. Thus to find the…

Q: 2. Write "most" under the compound which is most reactive toward electrophilic aromatic substitution…

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

Q: give the major products of each reaction

A: We have given three organic reactions.  Major product : the major product of reaction is the product…

Q: Please help me solve this synthesis. It takes 5 steps

A: OKAY, I will give complete synthesis by using 5 steps.  You can see step by step solution. How to…

Q: c) Circle the most electrophilic carbon in the structure below and explain your choice.

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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: The reaction shown here yields three different nucleophilic substitution products that are…

A: Nucleophilic Substitution reaction- The replacement one atom or group of atom from reactant…

Q: C. How many of the following structures are allylic? D. How many are arylic? E. How many are…

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Q: 4. Propose a reasonable mechanism, using curved arrow notation, for the following reaction. Be sure…

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Q: The structure of compound A is shown below. OH

A: primary carbon- carbon attached to  one carbon  secondary carbon-carbon attached to 2 carbons…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: The reaction is carried by Sandmeyer's reaction  Diazotisation of aniline followed by cuprous…

Q: 2) For two of the following pairs of compounds, identify the most basic atom in each compound, and…

A: Here we have to find the most basic atom and the most basic compound from the given pair of…

Q: Explain the below ? Carbanions are nucleophiles

A: Nucleophiles are electron rich species which donates electrons to electron deficient species. Eg.…

Q: Draw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as…

A:

Q: Follow the flow of electrons indicated by the curved arrows in the reaction and predict the product…

A: The possible product for this reaction shown below

Q: Describe three ways the following reaction can be carried out:

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Q: The product in this reaction is basic enough to be protonated by a dilute HCl solution. Draw the…

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Q: Possible product to this reaction

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Q: The reaction is a nucleophilic substitution, A is OH- and B is an alkyl bromide. Give the reaction…

A: The nucleophilic substitution reaction of alkyl bromide with OH- is given below

Q: Oxidize the below molecule as many times as possible. Then name each product. CI

A:

Q: A terminal alkyne is more acidic than an alkene and alkane because after deprotonation the lone pair…

A: Acidic strength of weak acid (organic acids) are explained by stability of its conjugate base…

Q: Consider the following reaction being performed with a low concentration. Think about what type of…

A: The product of the given reaction is

Q: Provide a name for each molecule. OH

A: Since you have posted a  question with sub-parts , we are entitled to answer the first three…

Q: 4. Which nitrogen in this molecule is the most basic? Explain briefly your choice.

A: Ans: Nitrogen "2" is more basic than all nitrogen.   Nitrogen is basic because it is one of the…

Q: Come up with a reasonable mechanism for the following reaction

A: In this question we want to draw reasonable mechanism for this reaction.  This reaction is Aldol…

Q: Describe two ways the following reaction can be carried out

A: Wolff Kishner reduction is a reaction to reduce ketones to alkanes. The reagent used to reduce…

Q: Explain (using resonance forms and words ) why compound 1 undergoes hydrolysis faster than compound…

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Q: CI

A: The detailed solution of your question given below_ Since, we know that the nucleophile attack in…

Q: Explain how an El reaction that generates an alkene may be reversible under the reaction conditions…

A: Here we have to explain why E1 reaction is reversible under reaction conditions but E2 reaction is…

Q: Explain why CH3CONH2 is a stronger acid and a weaker base than CH3CH2NH2.

A: Since the acidic strength of the compound depends on the stability of the anion formed by the…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: In this process, benzene sulfonic acid is reacted with aqueous sodium hydroxide. The resulting salt…

Q: Explain why a high reaction temperature favours elimination reactions, instead of substitution…

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

Q: 1. Illustrate and explain how the compound below can be used to produce different alkenes.

A: In this question, we will illustrating and explaining how the given compound ( which have alkyne…

Q: Et3N N. NH2 ZI O: O:

A:

Q: Draw the Substitution and Elimination Reactions:

A: In the substitution reactions, there is replacement of an atom or a group of atoms occur with…

Q: Both questions help please 1) ‘When a hydrogen halide adds to an asymmetrical alkene, the addition…

A: IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds

Q: Select the TWO most electrophilic carbons in this molecule. CI :

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Q: Part 3 out of 4 Select the compound that results from the reaction with following resonance…

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Q: 4. Predict the product and show the detailed mechanism for the reaction below. Use cyclohexane chair…

A: E2 elimination is elimination reaction where the rate of the reaction depends on both the reactant…

Q: Can you please help show how to use the given reactant in order to synthesize this molecule?

A: Alcohols react with alkyl halides to give an ether. Alkene undergo epoxidation followed by…

Q: The reaction that converts cyclopentanol into cyclopentene is a(n)

A:

Q: The SN2 reaction shows a reversible mechanism when the basic strength nucleophile and leaving group…

A: Generally SN2 reactions are substitution nucleophilic biomolecular reactions. The mechanism involves…

Q: b) Support your answer with the appropriate energy diagrams. (Energy diagram should show two…

A:

Q: H-CI

A: Protonation of alkene give more stable carbocation. Addition of chloride ion to carbocation gives…

Q: Write product and mechanism

A: Oxime reacts with H2SO4 to give caprolactam.

Q: (Chapters 5–13) For each of the following, 14. a. Label the reactive features, highlight the most…

A: Since you have asked a question with  multiple sub-parts, we will solve  first three sub-parts for…

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.