Using acetylene as your only source of carbons show how you would make 3-methylpentane

Q: Show the preparation of 1,2,3- triphenylpropene starting from benzaldehyde

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

Q: show how you would synthesize the chloride, bromide, and iodide from the corresponding alcohol.(a)…

A: Alkyl halides can be prepared by alcohols by many methods which are described as below- By action…

Q: Starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of…

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Q: Show how you would synthesize the following aromatic derivatives from benzene.(a)…

A: Alkylation of benzene will occur in the presence of t-butyl chloride and Aluminum chloride, which…

Q: 2. By using the same alkene, how do you synthesize the following alcohols? Give the alkene and show…

A: The formation of alcohol from the alkene with the same number of carbon atoms can be done by the…

Q: Starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of…

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Q: Propose a Synthesis of compound A from the starting material shown. As you plan your synthesis…

A: Let us discuss step by step mechanism of the following conversion.

Q: Starting with diethyl malonate, and using any other reagents of your choice, show how you would…

A: Starting with diethyl malonate, and using any other reagents of your choice, show how you would…

Q: How will you prepare 3-methyl but -1 – yne by starting with ethyne?

A: The reactants or reagents required to prepare 3-methyl but-1-yne by starting with ethyne are 1)…

Q: From the compound below, illustrate how will it be synthesized starting with benzene? Provide the…

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Q: Propose a synthesis of meso-4,5-octanediol starting from 1-pentyne. Specify the reagents you would…

A: NaNH2/NH3 : Abstracting acidic hydrogen CH3CH2CH2Br : Alkylating agent H2/Lindlar catalyst : Alkyne…

Q: Starting with acetylene and 1-bromobutane as the only sources of carbon atoms, show how to…

A: Given reaction,      5,6-Epoxydecane from acetylene and 1-bromobutane

Q: The ground rules are: you may start with anything that incorporates no more than 5 carbons in your…

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Q: Propose a method on how you will synthesize 5-methyl-4- octanol from 4-methyl-4-octene.

A: Hydration of alkene involves breaking of pi bond in alkene resulting in formation of a C-H and C-OH…

Q: Show reagents and experimental conditions to synthesize the following compound  from 1-propanol…

A: Acid-catalyzed dehydration reaction of alcohol with H2SO4 leads to the formation of alkene, the…

Q: ) From Benzene Show how you would make the following structure но. Br

A: Electrophilic substitution reactions are chemical reactions in which an electrophile displaces a…

Q: Show how you would convert 1-methylcyclopentanol to 2-methylcyclopentanol.

A: Given reaction,

Q: What change would you make to the above synthesis to prepare the trans-2-methyl-4-octene isomer?

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Q: Show how to make the following compound from propene? It may require multiple steps

A: Propene can be converted to 2-methylpent-2-ene by the following reactions. In the first step,…

Q: Using acetylene as your only source of carbons, show how you would make 3-methylpentane.

A: Applying concept of organic synthesis and reagent.

Q: Starting with acetylene and 1-bromobutane as the only sources of carbon atoms, show how to…

A: Introduction: Firstly, acetylene was treated with sodium amide and with 2 equivalent of…

Q: Using your reaction roadmap as a guide, show how to convert butane into 2-butyne. Show all reagents…

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Q: 2. Starting with butene, show how you could prepare butanoic acid in three reaction steps. 3. Write…

A: Dear student Since you have not mentioned any specific question no. here ,so I am answering question…

Q: Write a mechanism for the acid-catalyzed addition of water to: (a) 2-butene

A: Due to double bond character of the alkenes, they are electron rich species, therefore they can…

Q: Name the reagents you would use and in what order to convert 1-butyne to 3,4- dihydroxyheptane

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Q: Make 2-bromine, 4-nitro-benzoic acid, starting from benzene and using appropriate reagents.

A: Step-1: Friedel-Crafts alkylation Step-2: Nitartion, gives para product as major Step-3: Bromination…

Q: starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of…

A: Detail synthetic scheme for 3-octanol and a ketone are given below

Q: Show reagents to bring about the following conversions

A: A reagent is defined as the substance or compound that is added to the system so that a chemical…

Q: Show how you would synthesize fluorocyclohexane if you started with cyclohexane.

A: Direct senthesis of fluoro cyclohexane is not possible because Fluorine  is less reactive than…

Q: Using 1-pentene as your only source of carbon atoms, how would you use Gilman reagents to prepare…

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Q: 2. Using 1-butyne as the starting material, write the necessary reactions to convert to the…

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Q: Propose a method on how you will synthesize (a) 1-bromopentane from 1-pentanol and (b)…

A: In the organic conversion, various reagent converts the reactants into products. Reagents attacks…

Q: Show how you would make the following ethers, using only simple alcohols and any needed reagents as…

A: From nucleophilic substitution reaction we will prepared

Q: Show reagents and experimental conditions to synthesize the following compound  from 1-propanol  Q.)…

A: In primary alcohol, the -OH functional group is bonded to the carbon that has a nearby by the carbon…

Q: In this chapter, we studied the mechanism of the acid-catalyzed hydration of an alkene. The reverse…

A: In organic chemistry, The interconversion of the functional groups play an important role. The…

Q: How would you synthesize the following 3-hexanone from butanenitrile using reagents from the table?

A: Consider the given conversion as;

Q: Show reagents and experimental conditions to synthesize the following compound  from 1-propanol  Q.)…

A: The structure of 1-propanol is shown below: The structure of  2-Propanone is shown below: The…

Q: Show how you would convert toluene to 3,5-dibromotoluene in good yield

A: Direct bromination of toluene can't give 3,5-dibromotoluene in good yield because methyl group…

Q: Use a sheet of paper to answer the following question. Take a picture of your answers and attach to…

A: The nucleophile is CH3CH2O-.  The reactant, a conjugated enone undergoes an addition reaction by the…

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

A: Both the compounds are alkenes. An alkene can be transformed into a carboxylic acid by oxidation.

Q: Show how 2-butanone could be prepared by a procedure in which all of the carbons originated in…

A: Carboxylic acids are reduced to alcohols in presence of strong reducing agents. ,   PCC is mild…

Q: Using only propane as your source of carbon show how to synthesize 2-methyl-2-pentanol.

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Q: how would you try and make trinitrotoluene starting with benzene?

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Q: Propose a synthesis of 3-hexanone starting from acetylene and any other necessary reagents. Be sure…

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Q: In each case, show how you would synthesize the chloride, bromide, and iodide from the corresponding…

A: Halogenation of alcohols : The replacement of OH ( hydorxyl group) by a halogen is known as…

Q: Using acetylene as the starting material, propose a synthesis of 3-hexyne:

A: Alkyne can give a Nucleophilic Substitution reaction with an alkyl halide in presence of a suitable…

Q: Starting from ethyl chloride ,How will you prepare ethanol and n-butane?

A: To Find: synthesis method: i) Ethyl Chloride to Ethanol ii) Ethyl Chloride to n-butane

Q: Show how you would make the following ethers, using only simple alcohols and any needed reagents as…

A: Given compound,