[1] CH3CH,MgBr (excess) THE, ether [2] H3O*

Q: Devise a synthesis of attached product from the given starting material.  More than one step is…

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Q: Draw a stepwise mechanism for the following Friedel-Crafts acylation. CH3 AICI, + HCI CH

A: Given reaction,

Q: Draw a stepwise mechanism for the following reaction, one step in the synthesis of the…

A: The stepwise mechanism for the following reaction is given as- Here Grignard reagent (CH3CH2MgBr)…

Q: Draw a stepwise mechanism for the following reaction, a key step in the synthesis of the…

A: Proton abstraction from the acid HCl. Nucleophilic attack on to the carbonyl carbon by the lone…

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Q: Draw a stepwise mechanism for the following reaction of a Grignard reagent with a cyclic amide.

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Q: Draw a stepwise mechanism for the following reaction.

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Q: Draw a stepwise mechanism for the following reaction, which was used in the synthesis of ezetimibe…

A: Initially proton abstraction from alpha carbon to carbonyl group by LDA takes place. Formed anion…

Q: Draw a stepwise mechanism for the sulfonation of an alkyl benzene such as A to form a substituted…

A: This reaction is the electrophilic substitution reaction followed by basic medium

Q: Draw a stepwise mechanism for the formation of A from an alcohol and acid chloride. A was converted…

A: Since the alcohol group is having lone pair electrons and hence can attack on electrophile. Since,…

Q: Draw a stepwise mechanism for the conversion of lactone A to ester B using HCl in ethanol. B is…

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Q: Identify A in the following reaction scheme, and draw a stepwise mechanism for the conversion of A…

A: Compound A can be drawn as

Q: Draw a stepwise mechanism for the intramolecular Friedel–Crafts acylation of compound A to form B. B…

A: Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction.…

Q: Draw a stepwise mechanism for the sulfonation of an alkyl benzene such as A to form a substituted…

A: Stepwise mechanism for the sulfonation of alkyl benzene to form a substituted benzene sulfonic acid…

Q: Identify A in the following reaction scheme, and draw a stepwise mechanism for the conversion of A…

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A: The diester undergoes Dieckmann reaction in the presence of base to form beta-ketoester. The base…

Q: Draw a stepwise mechanism for the following intramolecular reaction.

A: The stepwise mechanism for the above intramolecular reaction has to be given below,

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A: A stepwise mechanism for the given reaction can be shown below

Q: Draw a stepwise mechanism for the following reaction.

A: In this reaction a fused ring system converted into a single ring system with the help of acid…

Q: Draw a stepwise mechanism for the following reaction.

A: The formation of electrophile (CH3)2CHCH2+ is shown below. This carbonation or electrophile…

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A: A mechanism for the given reaction can be shown as

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Q: Devise a synthesis of compound A from the given starting materials. You may use any other inorganic…

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Q: Draw a stepwise mechanism for the following reaction that forms ether D. D can be converted to the…

A: Since KOC(CH3)3 is a strong base. Hence it will take proton from the OH group and convert it into O-…

Q: Draw a stepwise mechanism for the following intramolecular reaction.

A: In this reaction, HCO2H acts as a source of proton.

Q: Draw a stepwise mechanism for the following intramolecular reaction, which is used in the synthesis…

A: The mechanism for the following reaction is as follows:

Q: Draw a stepwise mechanism for the attached reaction that forms ether D. D can be converted to the…

A: It is given that alcohol and an alkyl halide substrate are reacting to form an ether D, and further,…

Q: Draw a stepwise mechanism for the following reaction, one step in the synthesis of the…

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A: Given,

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A: The reaction of the carbonyl group with one mole of alcohol in the presence of the acid catalyst…

Q: Draw a stepwise mechanism for the conversion of lactone A to ester Busing HCl in ethanol. B is…

A:

Q: Draw a stepwise mechanism for the following reaction, a key step in the synthesis of linezolid, an…

A: Abstraction of proton from amide nitrogen with lithium.

Q: Devise a synthesis of each compound using 1-bromobutane(CH3CH2CH2CH2Br) as the only organic starting…

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Q: Draw a stepwise mechanism for the following reduction.

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Q: Devise a synthesis of each compound from aniline (C6H5NH2) as starting material.

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Q: Draw a stepwise mechanism for the formation of A from an alcohol and acid chloride. A was converted…

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Q: Draw a stepwise mechanism for the intramolecular Friedel–Crafts acylation of compound A to form B. B…

A: The stepwise mechanism is shown below,

Q: Draw a stepwise mechanism for the intramolecular Friedel–Crafts acylation of compound A to form B. B…

A: Friedel-Crafts Alkylation is used to alkylate aromatic compounds like benzene. This reactions makes…