propose the retrosynthesis of the following compound

Q: Supply missing reagents and prodacts in the following reaction schene. Ne mechani ple and disregond…

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Q: Mechanism. Studies have shown that aldol condensation can be catalyzed Propose a mechanism for the…

A: Various synthesis reactions are studied in organic chemistry. Aldol condensation is one of them. It…

Q: CH3 CH3

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Q: NaOEt, EIOH

A: Firstly we will discuss about Aldol condensation and Aldol Reaction.  Aldol condensation name is…

Q: 4. (a) Carry out retrosynthesis of the following compounds with forward synthesis as per the…

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Q: Propose a mechanism for the following rxn (give pdt if not given) HBr ROOR

A: Br is attached to allylic position in presence of an peroxide.

Q: Propose retrosynthesis and later synthesis LOCH3

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Q: Retrosynthesis of Ethyl (Z)-3-cyclohexyl-2-propenoate

A: Interpretation- Retrosynthesis of " (Z)-ethyl 3-cyclohexyl-2-propenoate " is to be proposed.

Q: CH3 N. CH3 Но Ph

A: For retrosynthetic analysis one has to identify the compound, should have the knowledge of…

Q: Show two Robinson annulation products

A: Let us discuss the reaction.

Q: Propose a retrosynthesis of the following compound using the michel reaction.

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Q: What is the major neutral organic product for the following sequence?

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Q: Give the reaction mechanism for the following: a. Aldol condensation b. Claisen condensation…

A: In an aldol condensation,  the enolate ion combines with a carbonyl molecule to produce a…

Q: Ph Ph ZI

A: Ans

Q: Show how the following targets can be formed via an aldol reaction of two carbonyl compounds using…

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Q: Show a reasonable mechanism for the following reaction (Hint: Michael addition followed by…

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Q: Provide such a synthesis plan for the retrosynthesis that follows. Any additional substances are…

A: We have to carry out the given retrosynthesis. The retrosynthesis is given below

Q: Write a reaction sequence of 4 steps and, afterwards, write the retrosynthesis

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Q: н. CH3 CH3ONA H3C CH3 CH3OH

A: Epoxide openning in basic medium is the SN2 reaction .

Q: Synthesize the target molecule on the right from the starting molecule on the left. Start with a…

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Q: CH3 H3C CH3

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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: (b) Provide the retrosynthesis along with forward reaction for the the following compounds as…

A: Retrosynthesis is the imaginary breaking of bonds of the molecule in such away that the molecule is…

Q: Propose retrosynthesis and later synthesis OCH3 OCH3

A: Retrosynthesis and synthesis are given below for following structure -

Q: Propose retrosynthesis and later synthesis

A: With the help of proper planning of various organic synthesis , we achieve the target molecule (the…

Q: Propose a synthesis for the following compound

A: To solve this problem we have to do it in multiple steps to get the desired product .

Q: Show

A: We will write the mechanism of aldol

Q: Busulfan is a cell cycle non-specific alkylating antineoplastic agent or simply a chemotherapy drug…

A: The final product is given below -

Q: Propose a synthesis.

A: The details solution for this reaction is provided below in attach image.

Q: (c) During Corey's synthesis of allomone he utilised the ketone shown below. Outline the…

A: The α,β-unsaturated carbonyl compound is identified by the presence of the double bond in the…

Q: Propose an efficient synthesis for the following transfor X (a) OF

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Q: Nitration of aniline is carried out after acylation because :Select one a. O-and p-products are…

A: Given,  Nitration of aniline is carried out after acylation because ? select one  a). o- and…

Q: г? НО

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Q: NH2 NH2 HNO3 H2SO4 `NO2 Major Product

A: Given,

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: 4. Provide a retrosynthesis only. Ph Ph Ph Ph

A: Retrosynthesis of the following compounds is given below.

Q: HO HO HO

A: For retrosynthetic analysis, one has to identify the compound, For identifying the compound in…

Q: retrosynthesis of the below targeted compound 'N'

A: Retrosynthesis is the process of breaking the target molecule imaginary in the mind in such a way so…

Q: он

A:

Q: For the following molecules, suggest two retrosynthesis pathways with their synthetic equivalents.…

A: Here we have prepare the following compounds by two retrosynthesis pathway

Q: here would you cut during retrosynthesis for the following molecule 4 1l ansuuers

A: Given target molecule is beta hydroxy ketone , which is product of aldol condensation reaction.

Q: CEN ОН

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Q: How To Synthesize a Compound Using the Robinson Annulation ?

A: Given:  Synthesize a Compound Using the Robinson Annulation

Q: Show the retrosynthesis and the synthesis of the following compounds: OH Target material Starting…

A: Dear student, the given question is a multiple question, hence I solved first question according to…

Q: 4. Provide a retrosynthesis only.

A: Retrosynthesis : at first three ethers are cleaved to give corresponding alcohols. Then functional…

Q: Propose retrosynthesis and later synthesis COOET EtOOC CH3

A: By retrosynthetic analysis, we actually try to move backwards on the synthetic line and try to reach…

Q: Provide a reasonable disconnection (retrosynthesis ) for the following Target Molecule and complete…

A: A retrosynthesis is the planning to form the target molecule (TM) which is complex in nature. The…

Q: CEN он

A: We have given that  Propose a multistep synthesis to prepare the following compound ?

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.