What is a correct mechanistic step of this reaction?

Q: e a short note on how to perform the Acree-Rosenheim reaction test. Make sure to mention the…

A: The Acree-Rosenheim test is performed in the chemical laboratory. Generally, the active reagent for…

Q: Could you help provide a complete curved arrow mechanism for this transformation?

A:

Q: What steps is needed to complete this transformation:

A: The complete transformation is

Q: HEAT

A: In this question, we want to draw mechanism for this reaction.  You can see details mechanism below.…

Q: What would be the major product if they are reacted with the reagents in the second column?

A: Since, you have asked multiple subparts questions, we will solve the first three subparts questions…

Q: alkylhalide in order of decreasing reactivity in an SN¡ reaction:

A: The order of reactivity of alkyl halides towards SN​1 reaction is-  Tertiary halide(3°) >…

Q: What would be the product of this ozonolysis mechanism? Would it be one product (the same reagent…

A: Ozonolysis of alkenes involves cleavage of carbon-carbon double bond resulting in the formation of…

Q: This

A: We will write the steps for given conversion

Q: H HCI

A: Welcome to bartleby !

Q: The correct product of this reaction is

A: Since we know that additional of HBr to alkene take place by ionic Electrophilic addition reaction .…

Q: What is the major product of the reaction at the photo?

A: In an aromatic nucleophilic substitution reaction, a nucleophile attacks on the carbon atom of the…

Q: Please

A: We will write all the intermidiate

Q: How does each of the tripling [RX] changes affect the rate of an E2 reaction?

A: INTRODUCTION: E2 reaction is also known as elimination bimolecular.It is a one step reaction.E2…

Q: draw the 2 products as a result of step-wise oxidation of the compound  above (image linked)

A: Alcohol is treated with strong oxidising agent to convert into carboxylic acid.

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: We know that SN1, E1 and SN2, E2 mechanisms follow the first and second order kinetics respectively.

Q: What is required in a typical transformation reaction?

A:

Q: scheme

A:

Q: Write the letters that correspond to the starting material ______ and the product ______ for the…

A: We have to determine the starting material and the product

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Supply the reagent for the…

A: The given reaction is: To identify the suitable reagent.

Q: What is the product of the below reaction?

A: This is a reaction where the alkynes are getting reduced to trans alkenes in the presence of Na,…

Q: Can you help propose a sy

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

Q: Which reagent(s) complete this transformation?

A: .When secondary alcohol  react with  oxidising agent  then convert into ketone . .Reactant name is 2…

Q: Which of the following is the most reactive in an E2 reaction?

A: E2 is bimolecular elimination reaction.

Q: Check any and all boxes to indicate which reagents can be used to carry out this transformation…

A: In this question, we have to choose the correct reagent for the given transformation.

Q: please help me to make synthesis of chrysin (5,7-dihydroxyflavone) in 4 or more steps and start for…

A: Chrysin is a dihydroxyflavon in which the two hydroxy groups are located at positions 5 and 7. It…

Q: In an SN1 reaction, what are the Stereochemistry Consequences: (Retained, Inverted, Lost,…

A: The SN1 reaction is one type of nucleophilic substitution reaction.  Basically, There are two types…

Q: Choose the reagent(s) that would be most likely to complete this reaction. Br

A:

Q: Which solvent listed below will result in the highest rate of this reaction?

A: Given reactant  is 3° butyl chloride hence it undergo through SN1 mechanism.  In SN1 mechanism…

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: What is the starting material in the reaction below?

A:

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

A: The shift occurs in ionic species .and the shift males the carbocation more stable.  In 1st…

Q: For each pair, which compound would be more reactive in a S?1 type reaction?

A: Given : Reaction mechanism is SN1.

Q: Br ОН - Br Но- + +

A: 1) Both reaction have same rate.  2) it is supported by polar aprotic solvents.

Q: write or draw the synthetic step to get to the following compounds. (Grignard reaction)

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

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: + HA Please write the mechanism arrows for it as an Sn1 mechanism please

A:

Q: Show the Reaction of 2° and 3° ROH with HX—An SN1 Mechanism ?

A: SN1 means Substitution nucleophilic unimolecular reaction, in this, the rate depends on only the…

Q: in this E2 reaction what is the major product

A:

Q: Check any and all boxes to indicate which reagents can be used to carry out this transformation…

A: the reaction is reductive ozonolysis, where alkene is converted to aldehyde and ketone group,in…

Q: Can you assist with identifying starting donor and acceptor compounds are needed to form the…

A: In this question, we want to identify Donor and Acceptor in Michael Reaction.  You can see details…

Q: Need help finding the order of Reagents  to form the product

A:

Q: Why are electrons easily available to the attacking reagents in π – bonds?

A: Pi bonds are formed by the sideways overlapping of the atomic orbitals and hence,the extent of…

Q: Provide a complete curved-arrow mechanism for this transformation

A: The above reaction involves 3 steps. The ester is first alkylated at the alpha position in the…

Q: Draw the product of the attached reaction:

A: In this reaction, OH- acts like base and it abstract the more acidic hydrogen and then negative…

Q: ?? Remember - can't use simple enolate/enol 7. for SN2 type reaction.

A: For addition to alpha to carbonyl compound, we have to convert that centre to nucleophilic centre.…

Q: which term describes the next mechanistic step in the catalytic cycle of the heck's reaction

A: A multiple choice question based on alkene, which is to be accomplished.

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

A:

Q: break down of this reaction in sequence and a complete reaction scheme

A: In the given reaction ferrocene is reacting with acetic anhydride in the presence of H3PO4 to…

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…