Show mechanism for Friedel–Crafts Alkylation Using a 3° Carbocation ?

Q: Show how to synthesize the molecule on the right, starting from the molecule on the left plus any…

A: A.  first alkyne is reduced partially to alkene by using Lindlar's catalyst. Then it is converted…

Q: Draw the product(s) for the following reaction

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

A: E2 elimination is a one step concerted mechanism reaction in which dehydrohalogenation (or any other…

Q: OMe Br H,N

A:

Q: What sequence of reagents can be used to accomplish th

A: The given reaction can be accomplished by the following steps 1. Bromination to form alkyl bromide…

Q: Draw the product for the following reaction.

A:

Q: D2. Draw the reaction full mechanism for TPCP. Carbanion Enolate HO Dibenzylacetone Вenzil но…

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Q: Draw a stepwise, detailed mechanism for attached reaction.

A: A detailed mechanism for the given reaction can be drawn as,

Q: Draw any product of dehydrohalogenation ?

A: The type of elimination reaction in which a hydrogen halide is removed or lost from the reactant is…

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: Show correct mechanism  for the starting material to product  A with curved arrows. For  product  B,…

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Q: Br Na C: CEN

A: Given reaction,

Q: Ho,

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Q: Retrosynthesis for: OH Br product starting material

A: Retrosynthetic Analysis or Retrosynthesis is a planned approach for organic synthesis reactions. The…

Q: Which alkyl halide would yon expect to react more rapidly by SN2 mechanism? an La or

A: A simple or primary alkyl halides are more suitable for SN2 mechanism. In SN2 mechanism, the…

Q: Show two Robinson annulation products

A: Let us discuss the reaction.

Q: What are the errors in the following answer?  Note: If the product has ortho or para substitution,…

A: In a substitution reaction, one substituent in a chemical compound is replaced by another.  When a…

Q: (c)

A: In this question we have to tell the major product of the Claisen rearrangement.

Q: how mechanism for synthesis of acetic acid using CH3COONa and HSO4

A: To illustrate: Mechanism for synthesis of acetic acid using CH3COONa and HSO4

Q: Draw the product for the following reaction

A: Solution

Q: Explain mechanism for the addition of two equivalents of HX to an alkyne ?

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Q: (thiongl chloride) SOCI2 HQ NaOH - H2D - HO. B. C, D, E (similar to problem with making unsummetniel…

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Q: Of the choices below, which two pieces will undergo a Robinson annulation to giv che product shown?

A: The Robinson annulation is reaction where the Michael addition followed by Aldol condensation takes…

Q: Circle one or more: SN1 SN2 E1 E2 OMs NaSPh, THF Mechanism:

A: Given reaction:

Q: Use Newman’s projection to predict the major product for an E2 reaction of the substrate shown…

A: Elimination reactions are those which convert saturated compound to unsaturated compounds for…

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: What alkyne (or diyne) yields attached set of oxidative cleavage products?

A:

Q: NaH

A: Aldol condensation : In presence of base when ketones or aldehyde reacts to another keto or aldehyde…

Q: Show mechanism for Vinyl Acetate (product) using Wacker Process Start with Potassium…

A: The process which is used for preparation of aldehydes and ketones from alkene is known as Wacker’s…

Q: 1. EtMgBr A 2. H*, H20 1. (Et)2CuLi 2. H*, H20

A: The mechanism of the following is:

Q: For each of the following pairs of substrates, which do you think will undergo an Sn1 reaction…

A: SN1 reaction is a nucleophilic substitution reaction . This reaction involves formation of a…

Q: one `H Benzaldehído Acetona Dibenzalacetona

A:

Q: 24. Propose an efficient synthesis for each of the following transforma Br (a)

A: The question is based on the concept of organic reactions. We have to convert the reactant into…

Q: What reagentls) will perform the following miction?

A: The given reagent is a ketone. It belongs to the carbonyl family. the IUPAC name of the compound is…

Q: Is TMS a good leaving group by itself? Can this all happen in one step? Please show the mechanism if…

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Q: ne major product?

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Q: Show the Reaction of ROH with SOCl2 + Pyridine—An SN2 Mechanism ?

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Q: Propose this mechanism

A: Given reaction,

Q: Draw the mechanism of how you can make cyclohexyl ethanoate from ethane

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

Q: Which substrate will go through E1 reaction fastest? Br Br A) B) ㅇ BY BV DJ ㅇ

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: alkyl halde The mechanism of this reaction is SN (SN2 or Sy1?). Explanation: Jvcleophile

A: SN2 reactions occur in a single step whereas SN1 reactions are those that occur in 2 steps. SN2…

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: show mechanism please using s like Sn1 Sn2 E1 E2 رے سلHo Но

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Q: raw the two aldohexoses and one ketohexose that can be derived from the enol shown below

A: Given : We have to make two aldohexoses and one ketohexose.

Q: ·NEN & shown below?

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Q: Question attached

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Q: transformation. OH Major synthesis Mini synthesis Draw a synthetic scheme to perform the following…

A: I have given the answer in the explanation section .Hope you will understand that.

Q: Possible aldol/claisen/conjugate addition question. Draw the final product. Show all work so I can…

A: Aldol condensation and claisen condensation are not possible here because carbonyl compound have no…

Q: practice problen ?

A: Please find the attachment.