Can you please draw out a complete curve arrow mechanism with the reagent and intermediate steps?

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 a multi-step synthesis with intermediate steps to produce the following molecule?

A: Multi-step synthesis of this molecule:The IUPAC name is 4, 5 dichloro 6, 6 dimethyl octane. The…

Q: HO,

A:

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: Given : a reaction and structure of reactant, intermediate and product.

Q: Draw the curved arrow mechanism for the following transformation. Show the mechanism that leads to…

A: NOTE: There is a small error in the reaction. The reactant will be an alkyl halide like bromide and…

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

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

Q: There is a missing reagent, provide a structure for it.

A: Dehydration means water get removed from molecule and alkenes are organic compounds containing…

Q: Copy the given reactions and supply curved arrows to account for the formation of the products.

A:

Q: Draw the FULL electron-pushing mechanism for the reaction, including ALL intermediates (with formal…

A: The ester hydrolysis mechanism for the given reaction is given below.

Q: Please provide a detailed mechanism (with arrows) for this reaction.

A: Here we have to provide the mechanism of synthesis of sulfathiazole-

Q: Draw all products, including stereoisomers, in the following reaction.

A: The given reactant is a 3° (tertiary) alkyl halide.

Q: + en

A:

Q: The attached reaction does not afford the major product that is given.Explain why this is so, and…

A:

Q: Image attached

A: Alkyl halides on reaction with strong base undergo elimination reaction. In product double bond…

Q: What is Lucas reagent made of? explain.

A:

Q: Can you help propose a sy

A: 1. Cyclohexane is converted in to cyclo-1,3-hexadiene :  cyclohexane upon treated with chlorine…

Q: Show the mechanism in propagation step of monobromination for Compound X below. Compound X

A: Halogenation of alkane: Alkanes can be halogenated in the presence of light or heat. The alkane does…

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: Can you help answer this problem and elaborate the steps clearly and show any reagent and…

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

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

A: Given:

Q: Could you please help draw a complete curved arrow mechanism with reagent and intermediate? I’m…

A: Base is needed to carry out the reaction as it will abstract alpha proton from Tiglyl CoA.

Q: Draw a curved arrow mechanism of the following SN2' reaction.  Make sure you show the intermediate…

A: In the given question we have to write following mechanism and intermediate involved in it.

Q: for

A: The reduction of carbonyl group to the methylene group to form hydrocarbon is done with the help of…

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: Please draw the missing product and the arrow pushing mechanism. Please identify all charged atoms…

A:

Q: Using

A: We will give mechanism of the reaction.

Q: H3C-NH2 но. „CH3 H3C-NH2 но. CH3

A: Ans

Q: Draw the final organic product for this reaction:

A: Here first of all , the base (NaOH) abstracts the proton from the diketone to produce an  enolate…

Q: What is the final product (D) of the following reaction sequence?

A: In the first step, p-chloronitrobenzene reacts with Fe/HCl followed by NaOH to form p-chloroaniline

Q: This reaction takes place via a pinacol rearrangement. Draw curved arrows to show the movement of…

A: Sulphuric acid(H2SO4) is used as dehydrating agent which rearranged ketones and also side products…

Q: Choose the major product of the following reaction sequence

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

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: d provide all the necessary reagents in class and any reagent

A: In Organic synthesis the reactant is converted into desired product using specific reagent

Q: он CN

A:

Q: Provide a curved arrow mechanism for the following reaction. CH;CH>OH + enantiomer

A: This reaction follows SN1 mechanism, In SN1 mechanism firstly leaves group leaves and carbocation…

Q: arrows

A: Ethylene glycol is a protecting group for carbonyl group and it will give acetal/ketal formation…

Q: Which is a correct mechanism step in the formation of an acetal?

A:

Q: ОН Br ОН

A: For synthesis, first we have to block acid and alcohol group as ester and ether respectively .…

Q: Friefly explain why the following synthetic step is incorrect, and rewrite it so that it is correct.…

A: Need to correct the product for the given reactant.

Q: This is a retro synthetic analysis problem, shown here is the final product (initial material is…

A:

Q: Write the correct mechanism and major product for a), and indicate the reagent needed for b) to…

A: Two question based on alkenes, which are to be accomplished.

Q: complete the following synthesis produces using a proper reagent and products

A: Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional…

Q: Can you show step by step of this missing reagent and show the synthetic intermediate?

A: Selective reduction of ester in present of ketone is done by NaBH4. We protect the ketone so that…

Q: Draw the Wittig reaction mechanism with arrow pushing.

A: Wittig reactions are helpful in alkene synthesis using aldehyde/ketones on treating with triphenyl…

Q: terminal alkene

A:

Q: Diagram 2: Compound Y.

A:

Q: Provide a curved arrow mechanism for the SN1 reaction below: CI CH3 H,C NACN

A: SN1 is a unimolecular nucleophilic substitution reaction. A carbocation is formed after the eviction…

Q: Use any reagent, mention it and complete all reaction steps in clear handwritten please!

A: The reaction given is,

Q: Find the diene and dienophile for the following product (retrosynthesis): ? + ? B B

A: Retrosynthesis: When Reaction  is carried out from product to Reactant side Then reaction is called…

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.