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

Q: The major product of the following reaction is он H,SO, heat

A: First lone pair of OH will attack on H of H2SO4. See the written solution.

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: Use the appropriate reagent used in the reaction. (d),(e) please!!

A: Here we have to mention the appropriate reagent for reaction d and reaction e-

Q: i See Periodic Table See Hint Add curved arrows to this enol structure to show the formation of the…

A: The carbonyl compound shows keto-enol tautomerism. One form can be converted into another form in…

Q: make sure reagents are CLEAR   write out the mechanism. make sure to include resonance, reagents,…

A: Friedel-Craft alkylation is the importnat reaction for the introduction of alkyl group on the…

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: Draw a reasonable synthesis for this reaction

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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: Determine the missing reactants in the two routes to form the above ether.

A: williamsons synthesis Alkyl halides reacts with sodium alkoxide to form ethers Ether functional…

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

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

Q: What alkyl halide and nucleophile are needed to prepare the attached compound?

A: Synthesis of Nitrile compound can be easily done via substitution reaction of alkyl halide with KCN.…

Q: но of For the following products draw in the correct two reagents using molecules from the above…

A: Reaction 1 is the esterification reaction where carboxylic acid reacts with an alcohol to form an…

Q: Complete the following multi-step synthesis.

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

Q: At which position in the final product is there an ethyl attached?

A: Given that : We have to identify the position of the ethyl group in the final product :

Q: I need a detailed reaction mechanism of this synthesis

A:

Q: In an unsymmetrical epoxide, the nucleophile attacks at the lesssubstituted carbon atom. Explain…

A: In an unsymmetrical epoxide, the nucleophile attacks at the less substituted carbon atom because of…

Q: (a) Consider the reaction below, and answer the questions that follow: UV ight (i) Draw a curved…

A: The reaction sequence given in the question represents a uv mediated ring closing reaction of a…

Q: Next, provide a reasonable mechanism for product formation using appropriate curved arrow notation.…

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Q: What reaction sequence would lead to the following transformation? ?

A: here we are required to predict the reagent needed  to carry out the following conversion.

Q: Explain how a student will able to isolate the mono eliminated product in good selectivity used in…

A: products are seperated on the basis of their physical properties.

Q: Draw the mechanism with curved arrows (Williamson Ether Synthesis). Please provide detailed…

A: Williamson synthesized the ether from alcohol

Q: Write a detailed mechanism f

A: Protonation of alkene  Attack of alkene as nucleophile (intermolecular reaction)   Deprotonation

Q: Hello, can you write the explicit formulas of A, B, C and D in the synthesis below?

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Q: The product (name) in the reaction with H20/ acid catalyst and H9SO4. Pls draw the whole reaction…

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Q: Please help me how to get this answer form this reaction. Can you show step by step and explain.…

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Q: Williamson Ether Synthesis Why does this reaction not work well for tertiary alkyl halides?  -…

A: Williamson synthesis is the process of formation of ethers. This reaction is a substitution reaction…

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: Examine

A: We will write the required information

Q: Explain and show how did the lettered compounds found in each reaction in letter a and b only. this…

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Q: Provide the IUPAC name for the missing compound in the reaction

A: In this question we have to tell the IUPAC name of the product.

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

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Q: arrows

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

Q: Design a reasonable synthesis for the following transformation. + C.

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Q: Fill in the appropriate reagent or starting material in each of the attached reaction.

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

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Q: Synthesize From

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

Q: Please provide a synthetic approach for the following reactions. Make sure to do the retrosynthetic…

A:

Q: ОН Br ОН

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

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

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Q: Please rovide a synthetic approach for the following reactions. Make sure to do the retrosynthetic…

A: Given that,

Q: Ph

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

Q: sentence.] КОН, ТHF (Name reaction?) N. ww QUESTION 13 Which reaction sequence will successfully…

A: Ans

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

A: Aldehydes are the organic compounds which contains the aldehyde group (-CHO). The reaction of…

Q: Show reagents and steps

A: Applying concept of organic synthesis and reagent.

Q: Explain Tautomerization with example?

A: Tautomerization

Q: Write product and mechanism

A: Oxime reacts with H2SO4 to give caprolactam.

Q: NO2

A: The organic reaction takes place in many steps. These steps involve the use of various reagents.