Predict the product of the following substitution reaction?

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: Draw the starting alkyne that would lead to this major product under these conditions.

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Q: OH 1. LIAIH4, THF OCH2CH3 2. H3O* HOCH,CH3

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Q: Nucleophilic Aromatic Substitution Draw the curved arrow reaction for this experiment showing the…

A: Solutions                               We Know that These products can be obtained from following…

Q: For each of the following pairs of species, encircle the stronger nucleophile in acetone?

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Q: Provide the mechanism for the 1st reaction in this synthesis: ВНЗ/ТHF

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Q: Add two curved arrows to the reactant side to illustrate the movement of electrons in the E2…

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Q: Following Curved Arrows to Draw a Reaction Product Follow the curved arrows and draw the products of…

A: This reaction is an elimination reaction  In which alkyl halide is converted into an alkene with the…

Q: True or false: the carbocation shown will undergo rearrangement. (Show your work and provide a brief…

A: The stability of the carbocation depends on the delocalization of the positive charge and the…

Q: Provide the mechanism for the 1st reaction in this synthesis: КОН

A: We have to draw the mechanism of given reaction

Q: detailed electron pushing mechanism fkr this reaction. It needs to be done as an SN2 reaction.…

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Q: Which one should be considered the major kinetic product of the following reaction?

A: Alkadienes electrophilic addition reactions 1. 1,2-addition : At lower temperature conditions…

Q: Show how a 1,2-shift forms a more stable carbocation from attached intermediate.

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Q: The major product of this question please

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Q: Draw the curved mechanism arrows that show the SN2 reaction of phenoxide with chloroethane and draw…

A: SN2 is bimolecular substitution reaction , which occurs in a single step and in this case no…

Q: The replacement of bromide ion to the iodide ion as a leaving group in the substitution reaction…

A: In the given problem, the nucleophile attacking is OH- and the leaving groups are Br and I. Since,…

Q: [H] N-H

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Q: scheme

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Q: Make one reaction scheme using proper compounds in the box below for Williamson ether synthesis.…

A: The reaction given is Williamson ether synthesis.

Q: Substitution with a(n) to an aromatic ring would result in reaction? Deactivator group, fast…

A: Activator - electron donating group  and para and ortho directing  Example - OH, OCH3 Deactivator -…

Q: Follow the flow of electrons indicated by the curved arrows in the reaction and predict the product…

A: The possible product for this reaction shown below

Q: What is the mechanism that leads to the circled, minor product? Is a hydrogen from one of the…

A: The alkyl halides are known for the direct bonding of the halogen to the carbon of the hydrocarbon.…

Q: Add two curved arrows to the reactant side to illustrate the movement of electrons in the E2…

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Q: Please help me, I have the mecahnism good but I am very confused on what the intermediate and…

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Q: Show a curved arrow mechanism for the formation of the major product below. major minor The…

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Q: For the reaction below provide all possible product(s) and circle the major product.

A: This reaction is Aldol Condensation reaction in the presence of acid water. You can see details…

Q: エース z-z L H H + CH Anything you need け。

A: Detail mechanistic pathway is given below

Q: Draw the major product of the reaction sequence. Omit byproducts. 1) C,H, MgBr, then H,O* 2) H, SO,,…

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Q: Now point out (Circle) the MAJOR CONTRIBUTOR(S) in you need consider all the resonances including…

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Q: Major product and mechanism for this reaction?

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

Q: Draw arrows to show a typical SN1, SN2, E1 and E2 reaction

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Q: Circle the better nucleophile in polar protic solvent. Below each answer, BRIEFLY explain your…

A: Polar protic solvents are capable of forming hydrogen bonding because they have atleast one hydrogen…

Q: What is the starting material in the reaction below?

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Q: Br2 undergoes electrophilic addition to maleic anhydride as shown here. Explain why this reaction is…

A: Here in this compound the C=C double bond is resonance stabilized by two keto group adjacent to…

Q: Draw the COMPLETE mechanism (including ALL curved arrows and final product) for the reaction below.

A: The given reaction is Diels Alder reaction .This is the type of Cycloaddition reaction .In this…

Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.

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Q: Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging…

A: Step-1 : 3-bromo-2-methylbutan-2-ol formation Step-2 : Epoxide formation Step-3 :…

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Which compound below undergoes…

A: Alkenes undergo addition reaction with HBr to form alkyl halide. The H+of HBr acts as an…

Q: The transform below undoes a nucleophilic substitution reaction. How would you carry out the…

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Q: There is at least one flaw in this synthesis scheme. Select the proper set of reagents from the…

A: The proper set of reagents to carry out the transformation given in the following step

Q: For the reaction below provide all possible product(s), and circle the major product.

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: CH3 H;C-C-i: CH, CH3 H,C CH,

A: SN1  stands for nucleophillic substitution reaction where rate of the reaction depends on only the…

Q: Circle the most acidic position in each molecule that could be deprotonated to give an enolate.

A: Enolate is an organic anion generated by the deprotonation of carbonyl compounds. Enols are 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: For each reaction below, show mechanism including curved arrows

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Q: . Complete the proper curved arrow mechanism for the reaction shown below. Br H-Br

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Draw the product by following the curved arrows. This reaction is an example of a [3,3] sigmatropic…

A: Sigmatropic rearrangement is shifting of sigma bond with the reorganization of pi-bonds in a system.…

Q: (e) Identify the Michael donor and Michael acceptor that could be used to synthesize this molecule…

A: The reaction in which nucleophilic addition of carbanion to an α,β-unsaturated carbonyl compound is…

Q: a) Show a detailed mechanism for the reaction to produce nitrogen gas and the two carbon radicals…

A: "Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: then

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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.