Supply synthetic routes to the following molecules using the indicated starting materials

Q: 5. Design a synthesis of the target molecule from the starting material shown. of ОН

A: Please find below the synthesis reaction.

Q: What is a multi-step synthesis with intermediate steps to produce the following molecule?

A: Multi-step synthesis of this molecule:The IUPAC name is 4, 5 dichloro 6, 6 dimethyl octane. The…

Q: OH 1. LIAIH4, THF OCH2CH3 2. H3O* HOCH,CH3

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

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Q: Which one of the molecules shown below prefers to exist as its enol tautomer?

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Q: Choose the best option for the diene precursor to the target molecule.

A: This is Retro Diels Alder reaction in which we have to find the diene and the dienophile.

Q: What would a possible synthetic route for the following reaction be?

A: To obtain the desired product we have to prepare vic.dihalide in cis position then reaction of this…

Q: Give the mechanasim Br₂ ccty HBr H₂02 НВО C

A: Reaction 1 : Br2 addition to alkenes produces trans -1,2-dibromo compound. Reaction 2 : HBr addition…

Q: what is the starting material using Diekmann cyclization reaction

A: The Dieckmann condensation is the intramolecular condensation reaction of diesters with base to give…

Q: Supply synthetic routes to the following molecules using the indicated starting materials

A: The synthetic route for preparation of 2-hexanol is as follows,

Q: Supply the missing reagent for the following ? Br

A: The terminal alkyne is acidic in nature

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: We know that SN1, E1 and SN2, E2 mechanisms follow the first and second order kinetics respectively.

Q: tow is benzophenone suited for nueleophilie aromaic abstitution Which positions and the be…

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Q: Provide an arrow pushing mechanism for the following reaction. Make sure to include initiation,…

A: It is a radical addition reaction. It is first explained by Karasch. It is also known as Karasch…

Q: SH 5 steps

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Q: Provide the appropriate reagent(s) for the following formation

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Q: What reagents, and or solvents/temperature belong below and above the arrow to produce the final…

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Q: Can you help propose a sy

A: 1. Cyclohexane is converted in to cyclo-1,3-hexadiene :  cyclohexane upon treated with chlorine…

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KI in acetone.

A: The addition of nucleophile and removal leaving group takes place in simultaneously in SN2 reaction…

Q: (a) Consider the reaction below, and answer the questions that follow: UV ight (i) Draw a curved…

A: The reaction sequence given in the question represents a uv mediated ring closing reaction of a…

Q: From pyridine and any other organic or inorganic reagent synthesize the following molecule

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Q: What reaction sequence would lead to the following transformation? ?

A: here we are required to predict the reagent needed  to carry out the following conversion.

Q: For the following reaction, draw the correct product that you would expect to form under Robinson…

A: Given - Product = ?

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: In substitution reactions, two mechanisms are, SN2 and SN1  . In elimination reactions, two…

Q: Provide the missing reagent to complete the following reaction. CH,CH,CH,ONa ? Write your answer on…

A: Alkyl halide reacts with sodium alkoxide ion to form an ether by the Williamson ether synthesis. The…

Q: b) A key piece in the synthesis is the molecule below. Provide a reaction that makes this piece that…

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Q: Choose the reagent(s) that would be most likely to complete this reaction. Br

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Q: Please provide a synthetic route for this molecule CH3 Ome

A: Synthetic route has been described.

Q: Please clearly draw the overall reaction taking place between methyl salicylate and sodium…

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Q: Please design syntheses that convert the starting materials on the left to the products on the…

A: Following is the synthesis of the given product from the starting material.

Q: HO HO,

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Q: What is a multi-step synthesis for the following:

A: The final product can be prepared in the following steps:Step 1 : Preparation of alkene from alkyl…

Q: Show all the arrow mechanism including the PROPER reagents.

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Q: Show the electron-flow mechanism of the chosen synthetic schemes. This involves predicting major and…

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Q: reagents

A: Friedel crafts alkylation reaction are mostly used in this question.

Q: Provide a synthesis for ethyl acetate starting with ethanol (shown above).

A: Given here ethanol molecule, and we are asked toprovide a synthesis for ethyl acetate starting with…

Q: H. H. CH3 CH,0 CH3 Sx2E2 CH3

A: It is an example of bimolecular nucleophilic substitution.

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: Determine the product of the reaction

A: In the hydro-chlorination reaction, first proton is added in the least substituted carbon then the…

Q: ) For your assigned letter rank the molecules provided from lowest (1) to highest (3) based on their…

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Q: Br2 and light CC14 solvent

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Q: H

A: Applying concept of organic synthesis via wittig reaction and organometallic.

Q: The following transformation is

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

Q: 2. Provide the missing reagents required for the synthetic pathway shown below: H3C-=-CH3 H3C CH3

A: In first step alkyne (butyne) is converted into cis-butene (alkene) with the help of either…

Q: The following Grignard reagents are desired: a) cyclohexylmagnesium bromide b) sec-butylmagnesium…

A: Grignard reagent falls under organometallic compounds and has magnesium bonded with halide or…

Q: он он H3C он HO, target compound starting material

A: Following is the mechanism of the product formation from the given starting material.

Q: Which of the following synthetic routes is the one that will most successfully generate a.

A: Alpha hydrogens are acidic in nature when base is used it is abstracted and gives conjugate base,…

Q: (e) Identify the Michael donor and Michael acceptor that could be used to synthesize this molecule…

A: The reaction in which nucleophilic addition of carbanion to an α,β-unsaturated carbonyl compound is…

Q: What is a correct mechanistic step of this reaction?

A: The given reaction is SN2  reaction because the  inversion of stereochemistry of reaction  occurs .…

Q: Br CH3-CC CH3 + 2HB1 CH3 C CH2 CH3 Br

A: Given reaction is addition reaction of alkyne. 2 moles of HBr is added across carbon carbon triple…