What reagents are necessary to carry out the conversion shown?

Q: Show how these conversions can be effected: Ethanol to propane nitrile

A: The conversation of ethanol to propane nitrile is shown below :

Q: Please find the product and provide the arrow pushing mechanism. Show all charged atoms and…

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Q: Draw the product of the reaction shown below. Use wedge and dash bonds to indicate relative…

A: In OsO4 reagent Osmium is in +8 oxidation  It is electron deficient it reacts wih electron rich…

Q: What series of synthetic steps could be used to prepare (CH3)2CHCHO from (CH3)3CH?

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Q: By means of a series of equations outline a method for carrying out the ff. conversions. You may use…

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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: Which of the following is a second chain propagation step in the free radical chlorination of…

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Q: Which method is suitable for converting 2-hexyne to (Z)-2-hexene? A. Na or Li in liquid NH3 B. H2,…

A: Alkynes are the organic compounds which contains at least one triple bond present in it. While…

Q: What is the major organic product of the following reaction?

A: Grignard reagent- Usually it is written as RMgX means alkyl magnesium halide. This is important…

Q: Design the synthesis of: (a) CH3C≡CCH2CH3 from HC≡CH and appropriate alkyl halides.…

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

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: Show how to make these deuterium-labeled compounds, using CD3MgBr and D2O as your sources of…

A: Deuterium-labelled compounds are produced when a D2 or D2O along with catalyst undergoes…

Q: Provide the starting material and reagent to prepare the following product as the exclusive product…

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Q: Write the appropriate reagents and products for each of the following reactions: ? ОН

A: Here we have to use dehydrating reagent to form the given product. We can use reagents such as- 1)…

Q: Draw the product of this nydrogenation reaction. Use wedge and dash bonds to indicate…

A: Interpretation: We have to determine the product for the following given reaction.

Q: CH2CI CH2CI CH2CI CH2CI CIH2C CH2CI CH2CI CH2CI A в D I. Which of the heterocycles would be the most…

A: Q2 i) Diels alder reaction refers to a chemical reaction takes place between a conjugated diene and…

Q: Please answer all three parts (a to c). a) Draw X. Assume that work-up occured. b) Step by step…

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Q: . Identify the product of the following reaction.

A: Hydro halogenation of alkynes: Addition of first equivalent (HBr) to terminal alkyne to give…

Q: Alkenes can be hydrated via the addition of borane to yield alcohols with non-Markovnikov…

A: In an organic reaction mechanism, a curved arrow represents the transfer of electrons. In an organic…

Q: Pick the reactant or solvent in each part that gives the faster SN2 reaction.a. reaction of -OH with…

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Q: Provide the reagents necessary to carry out the following conversion. Explain briefly what each step…

A: In given reaction reduction of epoxide to alcohol is done.

Q: Provide the appropriate reagents or product in the following examples.

A: Given ; reactant

Q: What synthetic goal is achieved by subjecting an alkene to an oxymercuration- demercuration reaction…

A: Alkene on oxymercuration and demercuration gives alcohol as a major product. This is addition…

Q: In base-catalyzed halogenation of acetone, how do you explain why the second (and third)…

A: # Halogenation of acetone takes place via the Enolate  formation in the basic medium. # the…

Q: In snythesizing diethyl ether from ethanol using concentrated sulfuric acid, increasing the reaction…

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Q: Which reaction intermediate is formed when 4-methylcyclohexene reacts with Br2 dissolved in CCl4

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Q: to convert (R)-2-chlorobutane to (S)-2-methoxybutane.

A: Given: To provide the reagents necessary to convert (R)-2-chlorobutane to (S)-2-methoxybutane.

Q: Provide the IUPAC name with clear explanation, as well as the retrosynthetic analysis and general…

A: Here we have to write the IUPAC name of the following given compound and it's synthesis from staring…

Q: Rank the compounds from most reactive to least reactive under conditions of both SN1 and SN2.…

A: Here we have to rank the compounds from most reactive to least reactive under conditions of both SN1…

Q: 1-butene Reagents Reagents n-butylbromide sec-butylbromide

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Q: Complete the following reactions by providing the missing structure(s). Answer must include a…

A: Introduction: Markovnikov rule: It describes the mode of addition reaction to the unsymmetrical…

Q: Provide the reagents necessary to carry out the following conversion. ОН

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Q: How might you bring about the following conversion? రు

A: In ozonolysis double or triple bond in an organic compound is cleaved by ozone. Intermediate of…

Q: Provide the reagents necessary to carry out the conversion shown. + HO OH HO

A: 1. O3 2. DMS 3. Na2Cr2O7/H2SO4/H2O

Q: Show how to accomplish the following conversion using reagents from the table. Br Br When only one…

A: To Solve this problem we have to complete the given reaction .

Q: Determine the reagents necessary to carry out the following conversion, and type them in the space…

A: Given reaction is, (E)-3methyl-3hexene ----> 3-methyl-3hexanol Here alkene is get converted into…

Q: reagents x and y are?

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Q: The following transformation is

A: The convertion of alkene to alkane can be done by hydrogenation of carbon carbon double bonds. The…

Q: Give the names of reagents and conditions for each of the reactions I and II

A: Alkyl benzene undergo two types of reaction  1) electrophilic aromatic substitution : Requires a…

Q: Give all possible hydration products of 3-methyl-1-hexyne. Show reaction and reagents

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Q: HO Он НО

A: The reagents necessary to carry out the given conversion has to be identified.

Q: Show the reagents and experimental conditions necessary to bring conversion in good yield.

A: Oxidising agents are used to convert alcohol to acids.

Q: Using the curve arrow symbolism, provide a step by step mechanism that accounts for the…

A: Here, polar protic solvent water is present. That's why under heating condition SN^1 mechanism is…

Q: what is the structure of D and E

A: In an organic reaction the  reactant convert to product using suitable reagent, with the change of…

Q: Complete the following nucleophilic substitution reactions. In each reaction, show all electron…

A: The reaction is completed by nucleophilic substitution reaction, where Br- is a leaving group and…

Q: The oxymercuration/demercuration of the compound (methylcyclohexene) below will form what product?

A: Oxymercuration-demercuration of 1-methylcyclohexene with water and mercuric acetate is followed by…

Q: Perform the following conversion using the wittig reaction. Also write the mechanism.

A: Wittig reaction  In this reaction the Aldehyde or the Ketone React with the triphenyl phosphonium…

Q: Provide the reagents necessary to carry out the following conversion. HO,

A: The product of this reaction can be synthesized via carbocation intermediate. For this we need: 1. A…

Q: each case below select the synthetic procedure/s that could be used to carry out the transformation,…

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Q: Show how to make these deuterium-labeled compounds, using CD3MgBr and D2O as your sources of…

A: Since you have posted a question with multiple subparts, we will solve the first three subparts 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.