Propose a reasonable mechanism. H*/ H2O

Q: Provide mechanism and major organic product. 1) NaOCH,CH3' CH;CH2OH 2) H30*

A: Given reaction is interanolecular reaction

Q: 1. NABH4 CI 2. H,O

A:

Q: H,0 HCI ()

A: The given compound is a heterocycle ,namely N-methyl-2-pyrrolidinone. It is a polar aprotic solvent,…

Q: NaO. + NaO Compound A

A: Attack of nucleophile to the carboxyl carbon of ester  Loss of leaving group leading to the…

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

A: Acetone/H+ reagent is generally used in sugar chemistry to protect diol. This reagent reacts with…

Q: Propose a mechanism. Br2, H20 H2C=CHCH2CH2CH2OH -CH2B.

A: Bromine reacts with alkene to form the bromonium ion. Since internal nucleophile (-OH) is present,…

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

A:

Q: CN NaOH HO H20 NC

A: Solution :         NaOH and water used as a reagent.NaOH is a base that is used to abstract…

Q: 5. Provide a complete, arrow-pushing mechanism which explains the observed re Br CH;CH2OH for

A: Organic reaction mechanisms.

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: The given reaction is,

Q: ден Please provide a mechanism for the following: а ден + Он Я ден H3C соон

A:

Q: Propose a mechanism for the following reaction:

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Q: Proposed a mechanism to determine the final product NEN CIO

A:

Q: Bonus: Propose a mechanism Must be perfect for any points NaOEt OEt EtO EtO HOE!

A: Given reaction,

Q: Qs1 Propose a correct synthetic route. Can be more than one. ÇOOH NO2

A: Since you have posted multiple questions in a single session, we are entitled to answer first…

Q: Propose a mechanism for attached reaction:

A: In this reaction, 'O' gets protonated to alcohol followed by the delocalization and the attack of…

Q: Please provide a synthetic route for this molecule CH3 Ome

A: Synthetic route has been described.

Q: Draw the mechanism ffrom benzaldehyde to this using:   i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+,…

A: Given,  The mechanism for target product formed from benzaldehyde by using  i)NaBH4 ii)TsCl, py…

Q: HCI H20 +

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: a) Propose a mechanism for the following reaction.

A: Given : structure of reactant and product.  This is a oxymercuration reaction.

Q: HN CH3B H,0 H* (cat)

A:

Q: ~NBU2 HO NaOH H. CI ELOH

A: The first step of the reaction involves the acid-base reaction. The NaOH being a strong base will…

Q: Provide a mechanism for the reaction below: H H. HCI

A: Chloromethylation is reaction of aromatic rings with formaldehyde and hydrogen chloride. The…

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: In intramolecular reactions, the reactive sites are present in the same molecule. The simplest…

Q: Provide the complete mechanism using Curved Arrow Formalism for the reaction of pyruvic acid…

A:

Q: Show the steps of the following

A:

Q: Draw a complete mechanism for the reaction below. HCI

A: Alkenes undergo addition reaction in the presence of hydrochloric acid, the addition follows…

Q: DBU OTs DMSO Me Ме Me

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

Q: propose a mechanism

A: In the given reaction OH- attack at carbon of CO group and negative charges generates at Oxygen then…

Q: Draw a stepwise, detailed mechanism for the attached reaction.

A:

Q: Propose this mechanism

A: Given reaction,

Q: N- HC(aq)

A:

Q: Draw a stepwise, detailed mechanism for the following reaction.

A:

Q: H,C-H,C-H2C-C C-H 2. HC H.

A: Terminal hydrogen of alkyne acts as acidic proton  Thus NaNH2  acts as base and carryout acid base…

Q: H₂O H₂SO4 ?

A:

Q: Write a detailed mechanism for this transformation. .O. HCI HO но HO НО H20

A: Carbonyl compound (aldehyde and ketone) reacts with an alcohol to form hemiacetal in the presence of…

Q: Draw a mechanism for the following reaction: Br t-Buo

A: The mechanism for the following question is- The tert-butoxide was used to form alkene by the…

Q: NO2 Propose an efficient synthesis NH2

A: We have to draw the product  for efficient synthesis as follows in step 2:

Q: Propose a mechanism for the following reaction:

A: In organic chemistry, there is a class of reactions that belongs to rearrangement reactions. This…

Q: Propose a mechanism for the following reaction:

A: Please find below the reaction mechanism

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: 3) Write a detailed mechanism of: CH CH. HNOT H'SO NO

A:

Q: H H H. H,C H,C H,C H,C H H3C. H3C

A: Interpretation: We have to draw the curved arrows mechanism for the given reaction.

Q: (d) Explain the observed stereo-selectivity in the formation of product using Chelation model. OMe…

A: The mechanism of this reaction is done in the below.

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: Draw the expected major product and the complete reaction mechanism for the following reaction. i.…

A: Ketones are the organic compounds that contain carbonyl group in a compound.

Q: H3Ç CH3 он он но. Но но Но

A: