How would you carry out the following reaction?

Q: Propose a plausible mechanism for the following transformation. OH [H,SO] MESH Mes

A: Sequence in the mechanism :-  Protonation of etheral oxygen Attack of nucleophile to the most…

Q: How would you carry out the following synthesis? ÇCH3 SO3H

A: We have to synthesis p-sulphonicacetophenone from benzene. Since both sulphonic and aceto group both…

Q: ÇOOH `NO2

A: Toluene is an aromatic hydrocarbon which belongs to the class of benzene which is also an aromatic…

Q: Predict the major product for the following reaction. H2SO4

A: Given reaction,

Q: Propose mechanism consistent with the following reactions a and b. HBr HBr ? b) регоxdes

A:

Q: OH H30* он

A: To show the mechanism of the following reaction

Q: Starting from ethane, provide a synthesis of the compound below showing all the reagents necessary…

A:

Q: 1. 98% H2SO4 Ме OMe Br- -78 °C 2. Li e ČO,Me OMe -78 °C-rt, THF

A: Robinson annulation followed by Quasi-favorskii reaction will give the desired product.

Q: b) Propose a detailed reaction mechanism for the following conversion. он Acetone HCI но но. -OH OH…

A: Acetone /HCl is used for the protection of syn-1,2-diol. For protection with acetone/HCl glucose…

Q: OH

A: This transformation in three step  Step 1  Protection of more reactive group( aldehyde)with 1,2…

Q: 1. Propose a mechanism to rationalize the following transformations. TSOH a) HO H2SO4 THE b)

A: Mechanism of organic reaction.

Q: Propose mechanisms for the reactions shown below. a. p-TSOH (cat) N- HN H. N- HN с. OCH3 но. o OCH3…

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

Q: How will you Synthesize benzyl the following morecule from bromide ?

A: In this question we will synthesized the given compound by using benzyl bromide  You can see details…

Q: 14. Propose a mechanism for following transformation. M₂O 0

A: In this question, we will write the details mechanism steps by using curved arrows for the given…

Q: What reagents will accomplish the following multistep synthesis?

A:

Q: How would you carry out the following synthesis of cyclohexane cyclohexanol cyclohexane

A: Note:Hey there! Thank you for posting the question. Since the question is not complete, the…

Q: OH Аcetone HO Но HCI HO- OH HO,

A: This reaction is protection of glucose with acetone.     Mechanism:   Step 1: In aqueous…

Q: Propose a mechanism for the following reaction:

A: The given reaction is represented as follows:

Q: Q17. (Continued) b) Provide the reagents needed to execute the following reactions. i) ii)

A:

Q: 17. Show how you would synthesize the reactions. a.

A:

Q: COH HO,

A: This is an example of homologation of alcohols

Q: -NH O2N

A: The heterocyclic compounds have a heteroatom such as oxygen, sulfur, nitrogen in the cyclic…

Q: CH NO2

A:

Q: Propose a mechanism for the following reaction:

A: Given reaction is

Q: 3. Propose a plausible mechanism for the following transformation: OH

A: Organic transformation in acidic medium:

Q: 5. Provide a mechanism for the following transformation: H2SO4 ÓH

A: We have to predict the mechanism for given reaction.

Q: 0. 1) СО2, Р, д 2) Н2О, H*

A: This is a klobe synthesis  in which major product is salicylic  acid

Q: c) Propose a mechanism for the following reactions. OH o BrMg MgBr HO ii) H20

A: Organic reaction mechanisms: Reaction of anhydride with Grignards reagent.

Q: Question attached

A: The way in which cyclohexane is converted to 1,3-cyclohexadiene has to be given,

Q: 3) Propose a mechanism for the following reaction. HO H2SO4

A:

Q: How would you carry out the following synthesis? CCH3 SO3H

A:

Q: Show how you might synthesize the following compound  from a haloalkane and a nucleophile.

A: Concept introduction: SN1 reaction: The displacement of atom or group by nucleophilic is known as…

Q: HO 20 we getRilum ierOH

A:

Q: How would you synthesize the following ether?

A:

Q: H20 ヤ

A: To the alkynes, the addition of water underogoes in the presence of a strong acid, usually sulfuric…

Q: iv) NGÔM, HO Heat

A: Note : Retro aldol followed by intramolecular aldol condensation. (For mechanism, see below).

Q: Propose a two-step synthesis for the following transformation. ? HO

A: Alcohols undergo dehydration to form ether. The reaction takes place via SN2 mechanism.

Q: Predict the product and provide the mechanism for the reaction below:

A: c) The given reaction involves the formation of enamine

Q: Propose a mechanism for the acid-catalyzed reaction below:

A: The possible mechanism explained below for this reaction.

Q: How would you carry out the following synthesis?

A: a. Friedel-Craft acylation followed by bromination then Grignard reagent preparation and then…

Q: 4) How do you perform the following reaction?

A: Applying concept of organic synthesis.

Q: OH H.

A: In the given transformation, carboxylic acid(-COOH) is converted to an      aldehyde(-CHO)

Q: c) Show how you would carry out the following transformations. (4 Marks) -HO-

A:

Q: но OH H-C=C-H

A: ->NaNH2 is a strong base which can abstract most acidic hydrogen . ->Na/liqNH3 can give trans…

Q: How would you carry out the following syntheses? (a) Br

A: Given are organic reactions.

Q: .Propose a synthetic route to carry out the following transformation. ? HO,

A: In this reaction acid react with alcohol in presence of acid to form an ester .  Here in this…

Q: How would you carry out the following reaction?

A: We have given that  Conversion of benzene to imine.  Imine :  imine  is  chemical compound…

Q: || CH3

A: Given,

Q: NO2

A:

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.