Show all working explaining detaillly each step

Q: ): In the space provided below please give the detailed mechanism for the following transformation.…

A: The reaction given is,

Q: Give a clear handwritten answer with explanation...give the mechanism of all sub parts  reactions…

A: 1) SN2 mechanism: Concerted mechanism with inversion of configuration 2) E2 mechanism: Concerted…

Q: fallowing What are theproducts reactions. Draw mechanis.m. and specify their stereachemistry- fthe…

A: since you have posted multiple questions in a single session, we are entitiled to answer only first…

Q: Provide to llaving Br a detailed, step by step mechanism for reaction OCH₂CH3 OCH₂CH3 OCH₂ CH3

A:

Q: Draw the mjor product of both question with mechanism asap

A: Given structure of reactants.

Q: O CH3CCH₂CH₂CH3 NaBH4/CH3OH

A: NaBH4 acts as a reducing agent by providing H- ion . It reduces Aldehyde into a primary alcohol and…

Q: Show all the steps necessay,in order to make each of the followring compoundS, Starting with benzene…

A: Preparation of 2,4-Dibromobenzoic acid from benzene can be done as follows:

Q: Rank the following species from best nucleophile to poorest nucleophile in an aqueous solution:

A: Nucleophilicity depends upon the tendency to donate electron pair. This tendency depends upon…

Q: a) Which of the following compounds is (are) capable of H-bonding to itself? Circle all that apply.…

A: Given compounds are: In the above given compounds, A is a ketone, B is an alkene, C is alcohol, D…

Q: Leite product and meehaniun PAGE NO. DATE:

A: Hoffmann bromide reaction is a type of reaction used for the conversion of amide to amine. This…

Q: Do all that's asked please label so I know

A: The question is based on molecular properties of the compounds. Lewis structure is a method of…

Q: Na OEt ELOH

A:

Q: ditions, and products for each step (you may set-up as retrosyntnesis ii you prefer). No chanisms…

A: Develop a multi-step synthetic route for the following transformation. Outline all reagents,…

Q: HO OH

A: Welcome to bartleby !

Q: HO. orion °° Y

A: To find: mechanism of the given reactions.

Q: (b) ethanol, HCI соон heat

A: Esterification reaction: Carboxylic acid reacts with alcohol in the presence of an acid catalyst to…

Q: complete the reaction, show detailed mechanism

A:

Q: Please give mechanism with name of all of compounds and product and all other steps

A: NaBH4 is mild reducing agent, as it is insoluble in non polar solvents, therefore alcoholic or…

Q: a How wod you prepar fulowing conpounds you may use any other magarta 777 LIAH, но HO Me MeMger

A: Reduction is the process of adding up of hydrogen atoms onto a functional group using certain…

Q: n two of uiese Teaction sequences will this transformation?

A:

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: Predict the product of photochemical ring closure of the three given, show the MO involved and…

A: Photochamical products findings

Q: Question: Provide the appropriate reagents. Please be as detailed as possible он но Et,N

A:

Q: (iii) Explain wvhy carbon shows a very high ability to catenate?

A: Catenation can be defined as the self-linking of atoms of an element to form chains and rings. This…

Q: Please answer with detailed mechanism and choose the reagent in all the steps.

A: The sequences of reaction given below

Q: TsO, Et,N: DMSO

A: Removal of OTs gives a carbocation which undergoes ring expansion via alkyl shift to produce another…

Q: Show all working explaining detailly each step Answer should be typewritten using a computer…

A: Rate of reaction is written as  Rate = k [NO]2 [Cl2]

Q: Prepare the following showing the stepwise mechanism: COOEt NH, 'N' H

A:

Q: write down adetaled mechanism for the fallowing transformations. CN

A: Thank you for submitting an excellent question but according to our code of honor only one question…

Q: 1. MeONa, MEOH 2. H3O* workup

A: The goes via enolization at first then intramolecular SN2 reaction followed by quasi-favorskii type…

Q: A. Catenation? B. Inert pair effect?

A: The explanation of the both the phenomena given in the following steps

Q: (c) Provide two different yet valid for the following retrosyntheses compound (with synthesis). off

A: Synthetic planning starts with the final product ( target molecule) , which is fixed and…

Q: Provide suitable strategy for obtaining NO2 from pyridine. Suggest mechanism.

A: To explain: the mechanism along with the reagents for the preparation of 4-nitropyridine from…

Q: prourde reagent tocary followng vans tormation. out the

A: Solution: Due to carbonyl carbon of ester it shows nucleophilic substitution reaction. This is the…

Q: What woud them mechanism be to go from cyclohexanol to methylcyclohexanol?

A: In order to prepare methylcyclohexanol from cyclohexanol we should follow the following steps:…

Q: from b.

A: For this transformation, oxidation of the alkene is carried out.

Q: Show all the steps necessanyyinorder, make eace of Hhe following Compaunds, Starting with benzene.…

A: The preparation of given organic compound from Benzene can be done as follows:

Q: CH₂OH H

A: Here we have explain major product formed in the following given reaction.

Q: O CN

A: Detail solution of retrosynthetic pathway and forward reaction is given below

Q: Show all working explaining detailly each step Answer should be typewritten using a computer…

A: Part A :- The change in enthalpy is the change in heat energy of a reaction Sum of product…

Q: BuLi

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

Q: o et o Et

A: The given reaction is an example of paternobuchi reaction. At first exciplex is formed and then…

Q: Outline the mechanism for the conversion of benzene to methylbenzene

A: The mechanism for conversion of benzene to methylbenzene is shown in the image below.

Q: Give major product part a,b,c properly

A: Solution- major product of given below with there reaction;

Q: most basic?

A:

Q: a.Work out the hybridization assert of both nitrogen atoms O B. Write the acronym of compound in…

A: DBU Is a Base which is used for Acidic Hydrogen Abstraction.

Q: In an early transition state the TS structure resembles?

A: A transition state is defined as a short-lived intermediate that is formed during a reaction and…

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.