If the H colored red is eliminated as H*, then two possible diastereomers can form. Draw the curved arrows for this electrophile elimination step, and draw each of the diastereomeric products. H He H20 + H3C-C-c~CH3 H

Q: - please break down each step as much as possible, draw all possible products and consider…

A: DMSO is polar aprotic solvent , hence it favours SN2 reaction  In SN2 reaction nucleophile (RCOO-)…

Q: Consider the nucleophilic substitution reaction shown here. (a) Argue whether this reaction takes…

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Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

A: SOLUTION: Step 1: The reaction of primary alcohol with HX to form haloalkanes follow SN2 mechanism.…

Q: Br NaOEt

A: Reagent used over here is NaOEt. This is a strong nucleophile and a strong base. So it will favor…

Q: Does either reaction produce multiple stereoisometric products? Which reaction occurs fastest? Does…

A: The reactions that involve the elimination of the leaving group belongs to a molecule by the…

Q: Draw a complete, detailed mechanism for the following 1. R'—ОН, Н reaction. R-C=N 2. H20, НО R OR'

A: The above reaction is an acid catalyzed reaction of nitrile with an alcohol which results in the…

Q: Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: The regiochemistry in the electrophilic addition reaction shown here does not adhere to the original…

A: Markovnikov's rule  : This rule is applicable in electrophilic addition in C=C double bond.…

Q: Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing…

A: Given reaction step:   For this reaction step, curved arrows have to be drawn.

Q: Draw curved arrows for the following reaction step. Arrow-pushing Instructions CH3 CH3 H-0-H H3C-C+…

A: This is SN1 reaction  When tertiary butyl chloride reacts with water forms carbocation and gives…

Q: Draw the product of this elementary step in an E1cb mechanism. Use the curved arrow mechanism to…

A: To solve this problem we have to write the mechanism of the given reaction .

Q: H. H2N-H + OH + H-CH3 + H-OCH, - H (ii) OCH2 + H20 (ii) OCH2 CH3 + но-сн

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Q: Determine the mechanism and draw the products of attached reaction. Include the stereochemistry at…

A: SN1  : It is the uni-molecular Nucleophilic Substitution. The first step of the mechanism is the…

Q: Draw a veasonable mechanism for this reaction that involves free radicals. CoH hv DH cat. OH Ph H,C

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Q: For each reaction, draw the complete mechanism and the major organic product(s), paying attention to…

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Q: CH,OH OH + CO2 H. OH H ОН OH ČH,OPO,2 ČH,OPO,2

A: First aldehyde to carbo

Q: Which EAS reaction is matched with the WRONG electrophile

A: We have been asked which electrophile is wrong for particular Reaction in electrophile aromatic…

Q: Draw the products of attached reaction and indicate their stereochemistry.

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Q: In this reaction, which species acts as the electrophile? Click on a letter A through D to answer.…

A: The species which act as an electrophile are the ones that are electron deficient. The species…

Q: Consider the interesting cascade transformation below. Provide a detailed mechanism including all…

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Q: Identify the cyclohexyl substrate which would undergo the slowest E2 with base.

A: To identify the cyclohexyl substrate which would undergo the slowest E2 with base.

Q: Br CH;SH

A: In protic medium Sn1 mechanism preferably occurs. At 1st step carbonation is formed after the loss…

Q: Draw the curved arrow notation and products for each elementary step described by the sequence shown…

A: CH3MgBr is  Grignard Regent, it is a nucleophilic reagent. They attack the electrophilic carbonyl…

Q: The following four reactions will be the focus of the upcoming chapters (substitution and…

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Q: H F LL H LL F F

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Q: Draw all possible products in the following reaction and circle the most stable product. Br КОН ELOH

A: In this question, we will draw all products for this reaction and the circle the most stable…

Q: Draw the products of each reaction by following the curved arrows.

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Q: Draw a complete, detailed mechanism AND prediet the major organic product for the follawmg trans…

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Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

Q: If H1 is eliminated from the carbocation shown here in an electrophile elimination step, then three…

A: In E1 mechanism, a carbocation is formed first and then a double bond by the abstraction of proton.…

Q: Draw a detailed mechanism that shows how the starting material is converted into each of the…

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Q: Draw the major product of this reaction. Include any relevant stereochemistry. Ignore inorganic…

A: Phosphonium ylides are used in the Wittig reaction, a method used to convert ketones and especially…

Q: If the anionic species shown were to eliminate a leaving group, the three possi- bilities would be…

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Q: 8.33 For each of the following substrates, predict whether a carbocation rearrangement will take…

A: A carbon atom which has a positive charge and three bonds is known as carbocation.

Q: hv D. C.

A: This is an example of 1,3-sigmatropic carbon shift followed by electrocyclic ring opening.

Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

A: Williamson Ether Synthesis:- It is the reaction between an alcohol and a strong base followed by the…

Q: Br2 H20 CH3CH,CH,CCH,Br CH,CH,CH,C=CH

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

Q: Question attached

A: In substitution reaction, a carbocation intermediate is formed. Sometimes, rearrangement reaction…

Q: For each pair of compounds determine which will undergo electrophilic substitution faster. (a) (b)…

A: As there are more than three parts of this question, we have solved the first three parts for you,…

Q: If H* is eliminated from the carbocation shown here in an electrophile elimination step, then three…

A: Given:

Q: Determine the mechanism and draw the products of each reaction.

A: (a) The structure of the given alkyl halide shows that carbon atom, on which bromine is present, is…

Q: 6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap…

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Q: Which reagent(s) will result in the nucleophile attacking the more substituted side of an epoxide?…

A: Given condition is nucleophile must attack to more substituted side of the epoxide.

Q: What is the most likely product from the following sequence

A: The first step of the reaction is the Friedel-Kraft acylation reaction and the second step of the…

Q: Draw the major 1,2-addition product and the major 1,4-addition product of the following reaction.…

A: The thermodynamic product is formed at higher temperature.

Q: Why does this epimerization step result in the preferred diastereomer? H TMSO- Ме Me TMSO- ÓMe ÓMe

A: When a pair of stereoisomers has no mirror image relationship of each other, then they are termed as…

Q: NaSMe Br

A: This reaction undergoes nucleophilic substitution SN2, when nucleophile attacked on bromine attached…

Q: v0 Draw a plausible mechanism for each of the following transfor- tions:

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Q: CI NaNH2

A: Benzyne is an unsaturated cyclic hydrocarbon derived from and structurally similar to benzene but…