How to get the molecule given below by getting out of bromobenzene and using the reagents you want? You synthesize? Show it.

Q: 5. Show a correct scheme (show all structures and reagents) that can be used to synthesize…

A: There are many steps involved in synthesising p-chlorophenol from benzene like electrophilic…

Q: a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of ethyl acetate. You…

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Q: Show how you would synthesize each compound from benzene, toluene, or phenol using the following…

A: Answer of the question given below,

Q: Give the reagents necessary for the synthesis above and please show the detailed step-by-step…

A: The reactant is Ethyl acetoacetate. The reactant contains the methylene protons which are highly…

Q: The most common application of Grignard reagents is the alkylation of aldehydes and ketones. For…

A: Grignard reagent is an organometallic compound because organic group that is alkyl or aryl group is…

Q: Propose a synthesis of the following molecule starting with benzene. Be sure to show all reagents…

A: The given compound is,

Q: Using the given starting reagents and benzene as the only source of carbon, perform the desired…

A: In the first step acetylene molecule will react with base NaNH2 and Cl2. acetylene chloride is…

Q: Indicate the directivity of the molecule below, and indicate if it is an 'activator' or a…

A: NO2(nitro group) is considered as an electron withdrawing group(EWG)

Q: How would you synthesize the following compounds from butanenitrile using reagents from the table?…

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Q: CN Br Na CN NaOH CN NaOH COOH Valproic acid

A: The solution is given below -

Q: Propose reagent(s) or product(s) for the attached transforamtion

A: Given Substrate is an epoxide. Reagent to the left (H3O+) leads to ring opening of epoxide in acidic…

Q: Use the starting material and any other reagents/solvents of your choice to synthesize the molecule…

A: In this question, we will synthesized the final organic product from the starting material alkene.…

Q: NH2

A: Naphthalene, on reaction with concentrated H2SO4 at 1600C gives 2-naphthalene sulfonic acid. On…

Q: Propose a synthesis of the compound shown below starting with benzene and any other acydic carbon…

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Q: Starting from benzene, propose a synthetic strategy that will synthesize the following molecule:

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Q: List the reagents needed to synthesize the following molecule in the correct order. (Beginning with…

A: The question involves concepts of Organic reactions. we have been given toluene. we have to convert…

Q: Minor product via E1 for 2-butanol and HCl?

A: Alcohol reacts with hydrogen chloride to give substitution and elimination reactions, depending on…

Q: This is the reaction I was referring to, I have no idea of what reagents can lead me to the…

A: In this reaction, the reagents are H2O and KMnO4.

Q: NH Phthalimide

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Q: Show the first step in the hydroboration mechanism using the reagents below.

A: In hydroboration - oxidation of alkene , there occur addition of H2O (anti-markonikov's addition) In…

Q: How would you convert the following compounds into butanoic acid using reagents from the table?

A: Organic conversions : 1. Alkylhalide with NaCN gives alkylnitrile further upon hydrolysis cyanide…

Q: Starting with phthalamide (below), provide a step-by-step synthesis of the amine shown below. You…

A: Formation of primary amine by Gabriel pthalamide synthesis. PCC oxidize alcohol to ketone. And…

Q: d. ethyl propanoate + xs NaBH4, later followed by acid e. butanal + 2 equivalents of ethanamine and…

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Q: and from H

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Q: Show how you could synthesize 3,5-dichlorophenol from phenol and any other reagent. он он CI

A: The question is based on the concept of organic reactions. We have to convert the given reactant…

Q: How would you perform the following syntheses? You may use any specialized organic reagents,…

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Q: : Starting from Benzene as the only organic reagent you have and use any other inorganic reagents to…

A: First step for synthesizing this compound is Friedel-Craft Alkylation reaction of Benzene: 1.

Q: Show how you would accomplish the following synthetic conversions. More than one step may be…

A: Answer  a) Cyclopentane + CI4           --H2O2 /Heat--->         Iodocyclopentane + HCI3

Q: For the compound below, propose an efficient synthesis using diethyl as a starting material. Provide…

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Q: (a) A useful synthesis of some diols includes the reaction of "bis-Grignard" reagents (compounds…

A: Organic  reactions:

Q: a) Show how to make the following ether starting from Propylchloride and 2-lodopropane, keep in mind…

A: The given ether can be synthesized by carrying out Williamson's Ether synthesis.  It is a SN2…

Q: Draw the structure of the two ketones which may be used to make the tertiary alcohol shown below by…

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Q: pentanal + 2 equivalents of methanol d. valeric acid + xs NaBH4 followed by acid

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Q: a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of ethyl acetate. You…

A: Ester formation can occur between acid and alcohol.  Self condensation meaning is between two same…

Q: When phenol is treated with Br2, a mixture of ortho-bromophenol and para-bromophenol is obtained.…

A: To synthesize ortho-bromophenol only from phenol.

Q: Propose a stepwise process for the synthesis of the benzene derivative shown below from benzene.…

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Q: The compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the…

A: The given structure of the compound appears as follows: The structural formula of the above…

Q: I. Propose a one-step synthetic route to get the following compound using only SN2. Explain. H3C=…

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Q: Use RSA, including disconnections, synthons and synthetic equivalents to show how to prepare the…

A: Detail synthetic scheme is shown below

Q: Show how you would syntheses 3-methoxybenzoic acid from 3-hydroxybromobenzene

A: 3-hydroxybromobenzene is treated with methanol, Williamson's synthesis takes place and a methoxy…

Q: Starting from Benzene as the only organic reagent you have and use any other inorganic reagents to…

A: The conversion acquires multiple steps. The Friedel craft alkylation of benzene followed by…

Q: Please help with the following: Propose a synthesis of the following molecule from the given…

A: Here we are required to synthesize the following diol

Q: Please fill in the blanks!! Which set of reagents (given below) would produce the products given in…

A: A Gilman reagent is defined as a copper and lithium reagent compound i.e. R₂CuLi in which R is an…

Q: Synthesis. Show how the compound below can be made from benzene and any other reagents of 4 carbons…

A: Solution -

Q: How would you perform the following multi-step syntheses using propiophenone, piperidine and any…

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Q: Please provide synthesis showing reagent  steps to get to the product compound. I appreciate your…

A: The transformation given is,

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.