A. Provide an efficient synthetic route to convert cyclohexanone to 1,2 cyclohexanediol B. Show an efficient synthesis for the following

Q: What would be the starting material needed to make tetrahydrofuran using a Williamson Ether…

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Q: + i) +CH3-MgX H30

A: Grignard reagent :- Alkyl magn esium halide (RMgX)  is called grignard reagent. It is highly polar…

Q: 2) Show an acceptable mechanism for the following transformation using proper curved arrows. HO

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Q: Design a two step synthesis that converts 3-pentanone into 3'-pentyl acetate as shown below. H2 -CH3…

A: we can convert  one functional group to  another by various reaction pathway like substitution or…

Q: What reagent did you use alongside with the peroxide on the first reaction?

A: Here, I have shown all the reagents that are involved in reaction one with names.

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. to make ethyl ethanoate using ethanol as the only organic reagent b. to make 2-…

A: In both of the process, ethanol has to be oxidised first and then the required conversions to be…

Q: HNO3 Zn A B D H2SO4 HCI or

A: The benzene undergoes an electrophilic substitution reaction. It has a high electron density, as it…

Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…

Q: Design a stepwise synthesis to convert cyclopentanone and 4-bromobutanal to hydroxyl aldehyde A.

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Q: Draw the missing organic structures in this short synthetic sequence. Assume an appropriate workup…

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Q: Show two different methods to synthesize alcohol A using a Grignar reaction.

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Q: Show how this cyclic ether compound could be prepared from an alkyl halide compound in an SN2…

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Q: Beginning with the correct organic halide and benzophenone show how one would prepare…

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Q: Why do we react β-naphthol with ethyl iodide rather than react ethyl alcohol with 2-Iodo…

A: we react β-naphthol with ethyl iodide rather than react ethyl alcohol with 2-Iodo naphthalene

Q: Draw the product of cyclohexanone, bromine and base catalysis. thank you for your explanation in…

A: The major product of the given reaction is illustrate here: Let the base is NaOH. We know that Br is…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: Please use 1,4-dimethoxybenzene and tert-butanol to draw a final product

A: Methoxy group is electron donating group so it is ortho-para directing group.

Q: turbo-Grignard reaction, please tell me the reason for reacting 2-chloropropane first. After that,…

A: The Grignard reagent is expressed as RMgX, Where R can be an alkyl or aryl group and X is a halogen…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: A carbonyl electrophile and an enolate (formed after the deprotonation of an aldehyde/ketone)…

Q: Cross-aldol reactions are a convenient route to synthesizing B-hydroxyketones and aß- unsaturated…

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Q: Show another SN2 reaction using a different combination of an alkoxide and an alkyl bromide that…

A: The different SN2 reaction that involves different combination of an alkoxide that is sodium…

Q: Show the arrow pushing mechanism for getting tropylium ion from the benzylic carbocation

A: In the given question we have to rearrange the benzylic carbocation to tropylium ion.

Q: Show a mechanism for how the product is formed. Your mechanism must use curved arrows to represent…

A: Given : organic reaction.  Here elimination is occuring, since weak base H2O is given, E1 reaction…

Q: Br + enantiomer ? ? b) "Br |= iodine

A: Answer:- this question is answered by using the simple concept of chemical reactions of organic…

Q: Show the combination of alcohol and haloalkane that can best be used to prepare   ether by the…

A: Williamson ether synthesis is the method of synthesis of ether by the reaction of alcohol and alkyl…

Q: (disconnect to a "diketone" (a) (b) (c) starting material)

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Q: Explain why alkylation of an α-carbon works best if the alkyl halide used in the reaction is a…

A: The alkylation reaction of an α-carbon depends on the R-X (alkyl halide) used in the reaction. The…

Q: (a) Show how ethanol and cyclohexanol may be used to synthesize cyclohexyl ethyl ether (tosylation…

A: (a) In the reaction, ethanol undergoes tosylation and a tosylate compound is formed. Then, William…

Q: 2. Write a synthesis of the Wittig reagent C1

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Q: Propose an efficient synthesis for the ff. transformations: b

A: a) Transformation 1 -

Q: fill in the product. which crown ether would be best to use in the following reaction to help the…

A: To dissolve the starting material, 18-Crown-6 with a molecular formula of C12H24O6 will be the best.

Q: write or draw the synthetic step to get to the following compounds. (Grignard reaction)

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

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: Why some substituents make a benzene ring react faster than benzeneitself (activators) ?

A: Directive influence of the attached substituents on the benzene ring The ability of the attached…

Q: Give a reaction you could use to convert Benjamin to aniline

A: Organic reaction mechanisms conversation of benzene into aniline.

Q: Perform a retrosynthetic analysis (please include - disconnection etc) and suggest a synthesis of…

A: The retrosynthesis method is used to determine the starting material by the fragmentation of the…

Q: Show a synthesis to the product starting from an alcohol

A: Ketones are synthesized by the oxidation of alcohol. Alcohol is oxidized by a variety of synthetic…

Q: Please complete the following conversion and show work in mechanisms. Name the final product and…

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Q: Explain why alkylation of an a-carbon works best if the alkyl halide used in the reaction is a…

A: The alkylation reaction of an α-carbon depends on the R-X (alkyl halide) used in the reaction. The…

Q: Show the reaction mechanism when phenol is reaction with a solution of Br2 and glacial acetic acid.

A: Phenol reacts with bromine and undergoes bromination reaction to produce p-bromophenol as major…

Q: Show the combination of alcohol and haloalkane that can best be used to prepare   ether by the…

A: Williamson ether synthesis takes place between an alkyl halide and the alkoxide ion. In general, it…

Q: Intramolecular reactions are also observed in Friedel–Crafts alkylation. Draw the intramolecular…

A: Friedal-Craft alkylation: It is a kind of aromatic electrophilic aromatic substitution that occurs…

Q: Note the major differences between the IR of the starting material(vanillin acetate) and the product…

A: The question is based on the concept of IR SPECTROSCOPY. we have been given IR spectra of reactant…

Q: Use retrosynthesis analysis, to get synthons and synthetic equivalents to show how to prepare the…

A: Answer is explained below. The synthons and the synthetic equivalents are as follows:

Q: F. Suggest a synthetic route for 2,4-dinitroanline, starting with benzene and appropriate…

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Q: Like acid chlorides, acid anhydrides react with alcohols in the presence of pyridine to form esters.…

A: Electrophile is electron deficient species whereas Nucleophile is electron rich species

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

A: Starting from benzene, nitration would yield nitrobenzene and further reaction with xenon fluoride…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: Aldol condensation: The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…