Hów will you accomplish the following conversions ? Give plausible mechanism in each case, identifying the important intermediates : (O Furan derivative from acetophenone bY Pyridine derivative by a four component reaction.

Q: Indicate the structure of product X and propose a detailed mechanism for its synthesis, under the…

A: The Grignard reagent reacts with acid chloride to form tertiary alcohol. Initially, one mole of…

Q: Identify the structure of the product in the following reaction. Provide a suitable mechanism with…

A: In this question, we will see the product and mechanism.  You can see below.

Q: Writethe mechanisms for each of the following reactions and briefly comment on the expected product…

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Q: An inexperienced graduate student treated dec-5-ene with borane in THF, placed the flask in a…

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Q: Provide the organic products of the following and also show the mechanism involved in (a)? (a)…

A: Wittig reagent (CH2=PPh3) has been used both the reaction .

Q: d) For each of the following pairs of structures, circle the stronger Brønsted acid. H´ `OCH3 `NH2…

A: Hello. Since your question has multiple parts, we will solve the first question for you. If you want…

Q: Which of the conditions below would provide the following transformation? ?

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

Q: 18. Suggest a plausible mechanism with structures of the following reaction: Br, H,0 CH3 CH2B.…

A: In the reaction mechanism of the above reaction, first the alkene will attack on the Br2 molecule as…

Q: + NH₂ H*

A: The detailed mechanism of following reaction is.

Q: 3, Suggest reactions to accomplish the following transformations in the forward synthesis direction.…

A: The retro-synthetic methodology deals with the schematic representation of the synthesis of produces…

Q: II) Propose a reasonable, selective synthesis of the compound below from benzene and any other…

A: Benzyl alcohol and 4-chloronitrobenzene are synthesized separately and then they are coupled in the…

Q: 1.

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Q: Predict the major products of the following reactions, and give the structures of any intermediates.…

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Q: When N-bromosuccinimide is added to hex-1-ene in CCl4 and a sunlamp is shone on themixture, three…

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Q: When cyclodecane-1,6-dione is treated with sodium carbonate, the product gives a UVspectrum similar…

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Q: A student in Ochem proposed the following synthesis. Explain the problem with this approach and…

A: LDA ( lithium diisopropylamide) is a larger base .Thus it accepts the it accepts protons from less…

Q: Proposeamechanismfortheconversionofcis-hex-3-enetotheepoxide(3,4-epoxyhexane) and the ring-opening…

A: The oxacyclopropane rings formed in the epoxidation process of alkenes are useful in forming diols,…

Q: c. Propose a synthesis for the compound D shown below, starting with benzene. Identify appropriate…

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Q: Complete the Reaction below and provide the following (i) a detailed stepwise mechanism to account…

A: When ketones react with primary amine they form imines.

Q: a. Propose a synthesis for compound D shown below, starting with benzene. Identify appropriate…

A: Here we have to propose a synthesis of the given compound from starting material from benzene in…

Q: Acetoxybenzene (PhOC(=O)OCH3) is much less reactive than ethoxybenzene (PhOCH2CH3) in electrophilic…

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Q: Suggest ways of synthesizing the following compounds, how would youmake the disconnections and what…

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Q: Propose a detailed, step-wise mechanism for the following transformation, make sure to SHOW all…

A: Desulfonation reaction In organic chemistry, the desulfonation reaction is the hydrolysis of…

Q: Give the products of, AND mechanisms of formation for, ALL reactions in BOTH synthetic schemes. OH…

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Q: Draw the major organic product(s) generated in the reaction below. Pay particular attention to…

A: Welcome to bartleby ! As per company rules we can't answer more than one question per session . So,I…

Q: CH

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Q: 2. Provide the product for the following reaction. Provide the sterochemistry an regiochemistry…

A: Hello. Since the question contains multiple subparts the first three subparts are solved. In case…

Q: NaOEt

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Q: An inexperienced graduate student treated dec-5-ene with borane in THF, placed the flask in a…

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Q: (i) What would you expect to be the order of reactivity from the following pyridine Derivatives…

A: Pyridines do not undergo (ES) electrophilic substitution reactions easily, they can do so when there…

Q: Give the major organic product(s) of the following reactions or sequences of reactions. Show all…

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Q: Me KO-Bu Me sO,Ar

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Q: Outline viable syntheses for the compound given below from the specified starting material. Please…

A: In this question, we will synthesized the compound which is naphthalene derivative and this is…

Q: What would be the product of the following reaction? Suggest a mechanism. H+

A: The reaction of a reactant thio-ester undergo acid hydrolysis is as follows, firstly lone pair of…

Q: Propose a synthesis for the formation of compound A below. Start with benzene and inorganic reagents…

A: Here we have to propose a synthesis for the formation given compound starting from benzene in…

Q: Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene…

A: The mechanism with all the proper steps has been explained in the image below.

Q: Nitrobenzene undergoes sulfonation to give three disubstituted products. One of the adducts is…

A: The reaction taking place is given as,

Q: 3. Provide the major organic product of the following EAS Reaction.

A: Given : structure of reactant EAS reaction happens according to activating group.

Q: b) Predict the major product of the following reactions and suggest mechanism. NO2 'BUOK CN CO2Et…

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Q: Predict the product of the following epoxide ring opening and provide a mechanism for its formation.…

A: Here epoxide ring-opening takes place in presence of an acid i.e. HBr. The product and mechanism…

Q: H,Cro, CH, NH, H+ NABH,CN -он -H NABH, но H- -он HO, CH,OH H H,C.

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Q: Give the expected products of the following reactions. Include a protonation step wherenecessary.…

A: Given reaction,         Cyclopentyloxirane with ethyllithium

Q: Suggest ways of synthesizing the following compounds, how would youmake the disconnections and what…

A: The following compound can be synthesized using esterification.

Q: (b) Suggest a synthesis of each of the following compounds, starting from suitable precursors.…

A: Carbene react with alkene to give corresponding cylcoproane derivatives. Reaction of carbene is…

Q: Proposing a plausible arrow pushing mechanism for the following transformation. Show all steps. H3O*…

A: In the above reaction, the double bonded O of the ester group will take proton first. Now the other…

Q: (S)-2-Butanol, CH3CH2CHOHCH3, slowly racemizes on standing in dilute aqueous sulfuric acid.…

A: Racemization is possible only when there is breaking and making of one or more bond connecting…

Q: Optically active 2-bromobutane undergoes racemization on treatment with a solution of KBr. Give a…

A: Optically active 2-bromobutane undergoes racemization on treatment with a solution of KBr. A…