ОН ОН н, аcetone CH3 H3C- H3C `CH3 НО ОН ОН НО glucose

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: Supply the missing compounds in the following synthesis scheme. 1. NaNH2 (3 equiv) H CCI4 Br2 1.…

A:

Q: Provide a mechanism for the following transformation. NH2 NaNO2/HCI/H,0 OH CH3 H3C- -CH3 H3C CH3 CH3…

A: Given : We have to make the product for the given reaction.

Q: Both of the following reactions will give the same SN2 product. Draw the mechanism for each of these…

A: SN2 reaction is nuclephilic substitution reaction of second order where a nucleophile attack at a…

Q: Propose a mechanism for the following reaction.

A: A mechanism for the following reaction has to be proposed

Q: Propose a reasonable mechanism for each product in the equations below. OH H2SO4 / H20 HO Br OH Br,…

A: First reaction is the epoxide ring opening in the presence of acidic condition and the hydroxide…

Q: Provide the mechanism and the product for the following reaction. (HINT – pyridine is a Brønsted…

A: In organic chemistry, the reaction can proceed via several pathways. The four major reaction…

Q: Propose a detailed mechanism for the following reaction: HO OH H₂SO4 O y

A:

Q: CCHCH3 CH30 H3CH2C е. CH2CH3 CH3OH

A:

Q: Propose a mechanism for the following reaction:

A:

Q: (CH3),COCH3 HI (CH3)½CI CH3I + + H20

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

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

A: Here I have shown a detailed mechanism of the reaction

Q: Propose a mechanism for the following reaction:

A: Furan is a heterocyclic diene. Br2 undergoes addition reaction with furan in CH3OH solvent which…

Q: Draw the Mechanism of Ether Cleavage in Strong Acid—(CH3)3COCH3 + HI → (CH3)3CI + CH3I + H2O

A:

Q: Propose a mechanism for the following reaction H2SO4 CH3-0-H OCH3

A:

Q: Give the major product of the following reaction. MeO H2

A: Given,

Q: H3C

A: Detail synthetic pathway is given below

Q: H,SO4 + CH3-0-H OCH3

A: The given reaction is the addition of hydro-alkoxy in an acidic medium. The first step is the attack…

Q: Propose a mechanism for the following reaction:

A: Please find below the reaction mechanism

Q: Draw a plausible mechanism for the following transformation. H2SO4 + NH,NH2 + 2H20

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

Q: H3CO. NaOH H3CO H3CO OCH

A: An aldol condensation is a reaction in which an enolate ion reacts with a carbonyl compound to form…

Q: HO NH2 H3O+ HO NH HO Но

A: 4-(2-aminoethyl)bnzene-1,2 diol reacts with acetaldehyde in the presence of acid, it results in the…

Q: Provide a mechanism for the following cyclization to make a spiroketal: H,SO4, H,O НО OH spiroketal

A: The reaction taking place is given as,

Q: HCI H20 +

A:

Q: Y.. HN HN MEOH, H2SO4 NaOH HO. Work through the above synthesis and draw the structure of compound…

A:

Q: H2NNH2, KOH Hао, heat

A:

Q: 1. (CH3CH2),CuLi 2. H20, H*

A: [As per rules only first question could be answered]   Organocuprate, a soft nucleophile, preferably…

Q: Propose a mechanism that accounts for the following reaction. H2SO4 OH

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: Propose a mechanism for each of the following reaction. (i) CH2-SMe2 Ph3 B PHCH2OH (ii) H2O2/ NaOH

A: The given reaction is, The mechanism for the reaction is shown below,

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

A:

Q: 2. Propose a stepwise mechanism for the following transformation, producing the observed…

A: Grignard reagent, RMgX is a useful reagent in organic synthesis. Where X be any halogen. Epoxides…

Q: Please state if the substrate below undergoes a carbocation rearrangement in an SN1 mechanism

A: In SN1  mechanism carbocation rearrangement takes place when that carbocation is not stable and and…

Q: Show the synthesis for the following Reactions. M Ô olt Nit2 Br -NH₂

A: Please find the attachment

Q: Predict the Retrosynthesis of the following compound : NH. OH CH -OH HOOC-CH2-NH2 + Do I H,C-NH-CH,…

A: Note: Epoxides are opened by alkyl amines. Therefore here the starting materials are oxirane and…

Q: Propose a mechanism for the following reaction.

A: In the above reaction, the reactant contains an acidic H. Hence the base NaOEt will take proton from…

Q: OEt 1. NaOEt 2. H3O*

A: The given reaction is,

Q: DBU OTs DMSO Me Ме Me

A: A question based on elimination reaction, which is to be accomplished.

Q: Draw a plausible mechanism for the reaction. CH-OoC,,H35 CH-OH 3 NaOH 3 CH-OO C17H35 CH-OH Nao…

A: ->-OH is nucleophile hence, give nucleophilic addition elimination reaction.

Q: Draw the products of the following reaction and show the mechanism; CH3-CH2-CCH3Br-CH3 + CH3OH

A: This is the SN1 reaction .

Q: Propose a mechanism for the following reaction:

A: Acid base reactions are faster and a base abstracts the most acidic proton.

Q: OH OH a) CH3 b) c) Br

A:

Q: Draw the complete mechanism and product of the following reaction. 1. NaOCH,CH3, THF 2. Br

A: In this Reaction alkylation is occurring at alpha hydrogen of ketone by using base (NaOC2H5) and…

Q: Show the complete mechanism for the formation of a hemiactetal, when 3-methyl-2-butanone eacts with…

A: Ketone with 1 equivalent of alcohol in acidic medium forms hemiacetal.

Q: Provide the mechanism for the following: CH3COOH + CH3 -OH O CH₂CH₂CH₂C CH3ÖCH₂CH₂CH3 + H₂O

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

Q: Provide the mechanism and the product for the following reaction. (HINT – pyridine is a Brønsted…

A: The given reaction undergoes from cyclic ester to cyclic amide with the help of given reagents.

Q: Draw the mechanism and predict the major product for each of the following reactions. (a) (b) O (c)…

A: The Reagents NaBH4 and LiAlH4 is a very good reducing agents which converts aldehyde or ketones into…

Q: Provide a detailed mechanism for the following reactions and determine the major product: HO. se +…

A: Note - The given question is a multipart question, hence I solved first three questions according to…

Q: Propose a mechanism for cach of the following reactions ОН H2SO4 + H2O ОН

A: This reaction is the dehydration of alcohol by the formation of carbocation as intermediate. Hence…

Q: Propose a mechanism for this reaction. CI + Cl2 + HCI CH3COOH (racemic)

A: The given chemical reaction is written as,

Q: Draw the product of the following nucleophilic substitution reaction and provide a full mechanism…

A: The substitution reaction is a class of organic reaction in which an atom or iron replaces another…

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.