Show how you would synthesize the following esters from appropriate acyl chloridesand alcohols. e) tert-butyl acetate (f) diallyl succinate

Q: N. d)

A: The question is based on the concept of organic synthesis. we have to identify the carbonyl…

Q: Show how an acetoacetic ester synthesis might be used to form a d@diketone such asheptane-2,6-dione.

A: Reactions in which an ester is alkylated at the alpha position to both carbonyl carbon atoms using a…

Q: Propose a mechanism for the following transformation when an ethyl magnesium bromide in excess was…

A:

Q: H. H.

A: We have to  Propose a synthesis for the following given compound,

Q: Show how you would synthesize the following alcohols by reducing appropriate carbonylcompounds.(a)…

A:

Q: Show how you would use anhydrides to synthesize the following compounds. In eachcase, explain why an…

A: a.

Q: Show how you would synthesize the following esters from appropriate acyl chloridesand alcohols.(a)…

A: Since your question has multiple sub-parts, we are solving only first three sub-parts for you. If…

Q: Propose an efficient synthesis for the following transformation. Hint: For the first problem you…

A: As there are two individual questions are given, only first question is solved here. Please re-post…

Q: Show how you would convert propan-1-ol to the following compounds using tosylateintermediates. You…

A: The starting material for given reaction is, We can transform an alcohol group into tosylate…

Q: Draw the reactant you would use to make the epoxide shown using a Sharpless epoxidation with t-BUOOH…

A:

Q: -0 0-

A: -> Acetal can formed when carbonyl compound reacts with alcohol in presence of acid .

Q: Show how you will carry out the synthesis of the following substances from benzaldehyde and any…

A:

Q: (a)

A: Given : Compounds of intramolecular aldol condensation To find : Products Solution : The given…

Q: How would you prepare the following ketones using an acetoacetic ester synthesis?

A: Acetoacetic ester synthesis involves the formation of alpha substituted acetone.

Q: Show how you would use anhydrides to synthesize the following compounds. In eachcase, explain why an…

A: The use of anhydride to synthesize the give compound is shown as,

Q: Show how you would convert propan-1-ol to the following compounds using tosylateintermediates. You…

A: Given: Ethyl propyl ether

Q: Show how you would convert aniline to the following compounds.( b) chlorobenzene

A: Given conversion,

Q: OEt acetoacetic ester

A: The given synthesis is an example of synthetic uses of acetoacetic ester.

Q: Show how you would synthesize the following esters from appropriate acyl chloridesand alcohols.(a)…

A: The following esters can be prepared as follows:

Q: Propose a mechanism for each of the following reactions:

A: Please find below the mechanism for reaction a. Note : The rearrangement of carbocation happens only…

Q: g) h) N

A:

Q: Starting with acetoacetic ester and any other reagents propose a synthesis and a mechanism for the…

A: In this question, we want to Synthesized the Final Product by using Acetoacetic ester.  You can see…

Q: Propose a mechanism for each of the following reactions:

A: a) Let us see the mechanism for the reaction In the above reaction, 95% of the product formed is…

Q: Show how the following ketones might be synthesized from the indicated acids, usingany necessary…

A: This is the reaction given

Q: Show how you would synthesize the following:  cyclohexylmethanol from an alkyl halide using an SN2…

A: The above conversion can be bought bouth by the following reactions.

Q: `N' H

A: This is synthesis of indole from phenylhydrazine and cyclopentanone

Q: S Na* SCH CH3 a thioester ethyl thiolate

A: It is a general case of attack of RS- nucleophile on Electron deficient Carbonyl Carbon to form…

Q: Show how you would synthesize the following esters from appropriate acyl chloridesand alcohols. (c)…

A: Given   The given compounds are benzyl benzoate, cyclopropyl cyclohexanecarboxylate and acyl…

Q: Show how you would accomplish the following synthetic transformations. You may useany necessary…

A: Given conversion, pyrrolidine to N-ethylpyrrolidine

Q: Show how you would use direct alkylation to synthesize the following compounds.(a)…

A: Benzyl trimethyl ammonium iodide can be prepared by the direct alkylation reaction of benzyl amine…

Q: Show how the malonic ester synthesis can be used to prepare the following substituted acetic acid

A: Given compound,

Q: b) Show a complete reaction mechanism for the synthesis of compound K via malonic ester synthesis.…

A: We need to synthesize compound K via malonic ester synthesis.  The reaction is attached in the…

Q: Show how to synthesize the following compound  using either the malonic ester synthesis or the…

A: The malonic ester synthesis of 2-Propyl-1,3-propanediol undergoes a nuclophilic attack using strong…

Q: Show how you would synthesize t appropriate acyl chlorides and alco a) ethyl propionate b) phenyl…

A: The given product is cyclopropyl cyclohexanecarboxylate.

Q: Propose a mechanism for the following reaction. КОН in MeOH

A: Robinson annulation: This method is used for the formation of six membered ring by creating three…

Q: Show how you would use direct alkylation to synthesize the following compounds.(a) pentan-1-amine

A: The structure of pentan-1-amine is shown below.

Q: Show how you would use direct alkylation to synthesize the following compounds benzylamine

A: SOLUTION: Step 1: Reaction of benzyl chloride with excess of ammonia results in the formation of…

Q: Claisen condensation of ethyl isobutyrate.

A: It is an organic coupling reaction which results in formation of a carbon-carbon bond between either…

Q: 0 OMe

A: Here we have to synthesize the following given compound by two canbonyl condensation reaction.

Q: Draw a complete mechanism using arrows to show how the following ylide is formed from Ph3P and…

A: In the given example, PPh3 can be considered as a nucleophile which replaces the halogen atom to…

Q: Show how you would synthesize the following derivatives from appropriate carbonyl compounds. (b) (c)

A: The carbonyl compounds on treatment with amines forms Schiffs bases.

Q: What starting materials are required to synthesize the following compound, using the Fischer indole…

A: Fischer indole synthesis is mainly the cyclization of arylhydrazone which is made from arylhydrazine…

Q: Show how you would synthesize octanal from each compound. You may use any necessary reagents.(a)…

A: The preparation is depicted as follows,

Q: Draw the structures of the nucleophilic B-keto ester and the aB-unsaturated ketone acceptor that…

A: The retrosynthesis of the given compound gives us the nucleophilic beta-keto ester and alpha-beta…

Q: 1. Provide a detailed mechanism for the following reaction and give the structure of the product 1.…

A: This equation contains  multiple Questions so for multiple Questions, I will just give first…

Q: Propose a synthesis for the following transformation. OEt H' HO,

A: