Show mechanism for Vinyl Acetate (product) using Wacker Process Start with Potassium tetrachloroplatinate and use Acetic Acid to be the nucleophile.

Q: Please transform and give starting material or product. Show stereochemistry and mechanism as…

A: In this question, we will give the product and Mechanism. You can see details Solution below.

Q: Draw mechanism for fischer esterification using the reagents benzoic acid, methanol and sulfuric…

A: Given : Fischer esterification using the reagents benzoic acid, methanol and sulfuric acid. To find…

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: What is the reaction mechanism for

A: gyi

Q: what is the polymer formed when resorcinol and formaldehyde are combined with naoh? Shows complete…

A: Please find the below attachment.

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: Explain why the following reaction sequence will not occur:

A: -NH2 is an electron donating group. Hence, it increases electron density more on ortho and para…

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: Need help. Please draw out mechanism on how to get the product.

A:

Q: Show the mechanism for this reaction using arrow pushing

A: Friedel craft alkylation  Catalyst AlCl3 Carbocation stability…

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,…

A:

Q: Ho,

A:

Q: Is it possible to synthesize from these two when cutting in this way? Also, please explain the…

A: The provided retrosynthesis will not work for the synthesis of given target molecule. This…

Q: Select the electrophile (A, B, or C) in the following reaction step.

A: Electrophile is an electron deficient species or a neutral compound having an incomplete octet or…

Q: show the mechanism for the reaction

A: The reactions involving organic compound are called organic reactions.  Reaction mechanism gives the…

Q: e the product from the following reaction sequence?

A: The product of the given reaction sequence can be drawn as

Q: Show the full mechanism for the following reaction.

A:

Q: Show the mechanism

A:

Q: Complete the following multi-step synthesis.

A: Nito benzene upon nitration agin it give meta-dinitrobenzene , it  reduced selectively with NH4HS…

Q: Complete the following reaction scheme , Complete the following reaction scheme

A:

Q: What is Lucas reagent made of? explain.

A:

Q: Propose stepwise mechanism of following reaction.

A:

Q: Hept-2,5-dione + OH- = ?  please show mechanism too...

A: This reaction proceeds via an intramolecular Aldol mechanism to form a beta-hydroxy five-membered…

Q: Provide the retrosynthesis and a forward synthesis for the transformation from the starting material…

A: Synthesis: Step 1: Dehydrobromination using NaOEt. Step 2: Epoxidation using mCPBA. Step 3: Acid…

Q: NH, но Br

A: The given compound contains an alcohol functional group and bromine substituent. In presence of…

Q: Draw the arrow pushing mechanism of the following reaction

A: Given substrate is 3°alkylhalide hence in presence of polar solvent and heating conditions favours…

Q: Draw the product and show the mechanism

A: We have to draw the products and show the mechanism for the given reactions.

Q: Please show mechanism and explain every strep

A: We have to predict the mechanism for given reaction

Q: Topose a synthesis of the aldehyde using ethane and propane as your only sources of carbon atoms.…

A: Since you have posted multiple questions in a session, as per guidelines we are entitled to answer…

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: NaH

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

Q: draw a complete synthesis from starting material. List out all solvents and reagents used and draw…

A: Here we have to write the major products formed in the following sequence of reactions.

Q: Draw the step-by-step mechanism using curved arrows of the following reaction in acidic condition.

A: NaOCl in an acidic medium acts as an oxidizing agent. The given reactant is;

Q: Can you please draw me the synthetic route (not mechanisms) for this reaction by using…

A: Step I : conjugate addition of OH to unsaturated ketone. Step II : it is an haloform reaction in…

Q: 3. Name other two reagents which are used for acetylation. Give mechanism for each reagent.

A: Acetic anhydride and acetyl chloride are two reagents for acetylation of aniline.Mechanism for…

Q: Show the reaction mechanism methyl magnesium bromide with propanal and also propanone

A: SOLUTION: Step 1: Propanol reacts with methyl magnesium chloride and further hydrolysis gives…

Q: major ProdvCtS on only -ome H3PM, anes Et, NH

A: in organic chemistry functional group can be converted to another functional group via certain…

Q: Synthesize From

A: The acidic proton in the ketone substrate can be abstracted by the base in order to generate…

Q: Propose Mechanism to get the follwing synthetic target

A: An organic reaction mechanism is a complete step by step account of how a reaction of organic…

Q: BuLi

A: Organolithium is a reagent that acts as a base or nucleophile in the reaction as per the given…

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

A:

Q: Draw the synthetic pathway including reagants + products

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

Q: mechanism for the following reaction

A: Given reaction: A mechanism for the given reaction can be drawn as

Q: Show the mechanism for the following reaction

A:

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

A:

Q: Select the major product of the reaction:

A: The answer to the following question is-

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

A: Friedel-Crafts alkylation: This is an example of electrophilic aromatic substitution reaction. When…

Q: practice problen ?

A: Please find the attachment.

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.