OH Ph PhMgBr OEt Ph

Q: Draw a reasonable mechanism for the following reaction HO-S=0 HO OH OH

A: In this question, we will draw mechanism for each Reaction.

Q: (d). 1. MgBr 1. O3 (2 equivalents) 2. Me,s 2. H20

A: Organic compounds in which two carbon atoms of a hydrocarbon chain are bonded to each other by a…

Q: Select one deactivator & ortho para director to be on a benzene ring to start.  You will then add a…

A: Ortho- para structure on benzene ring is given as follows -

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

A:

Q: Provide the mechanism for the 1st reaction in this synthesis: ВНЗ/ТHF

A:

Q: NH2 Br ETONO + COOH Br Heat

A: The given reaction is an example of [4+2]-cycloaddition reaction. Firstly, the two reactants will be…

Q: (CH3)3SICI ZnCl2

A: Synthesis and reaction of enolate.

Q: 1. NABH4 CI 2. H,O

A:

Q: Draw a mechanism for this reaction: CH3 H,C-OH Br CH3 ČH3

A: The above Reaction is the Nucleophilic substitution reaction of the allylic Halide . In this above…

Q: H,0 HCI ()

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

Q: ive the complete mechanism for the reaction below. The major product should be that of something…

A:

Q: (b) OAc HOAC MsO

A:

Q: AGNO, 1. Draw out each reaction mechanism that occurs to create each respective product shown in the…

A:

Q: Draw the complete, detailed mechanism for the following reaction.

A: Base abstracts a hydrogen atom from CH3NO2 and it generates a good nucleophile (-CH2NO2). This…

Q: OH H2SO4 (cat.) H20

A:

Q: NaOH NH, + NH3 H20

A:

Q: Draw out the complete mechanism of the reaction and include all relevant electrons and arrows…

A: It is given that in the reaction benzaldehyde and acetone are the substrates which are undergoing a…

Q: 3. Write a detailed reaction mechanism for the following transformation. Upload your answer as an…

A:

Q: OH H2SO4 Нeat

A:

Q: In the following synthesis, there are 5 steps that must be done in the correct order (i.e. Step #1,…

A:

Q: HO 1. LIAIH4 2. H20 HO HO HO.

A: Mechanism

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 reasonable mechanism for the following reaction CX НО, OH H₂SO4 (cat)

A: Basically this reaction ia used in protection of aldehyde and ketone in order to prevent the…

Q: Circle the reactant that is a nucleophile and draw the mechanism using the appropriate arrows for…

A:

Q: Rank the following bases in order from slowest E2 reaction rate to fastest. ONa H20 NaOH NH3 OK ONa…

A: Nucleophiles which are strong bases are likely to undergo elimination over substitution. Bulky…

Q: Give a complete mechanism for the following Reaction: CI NH2 NH2 NANH2 / NH3 ČH3 ČH3 CH3

A:

Q: Draw a complete, detailed mechanism for the following reaction. A key intermediate is provided.

A: The mechanism for the given transformation has to be determined.

Q: Heat Benzaldehyde + KCN + EtOH

A: Concept introduction: Benzoin condensation: It is the coupling reaction that is occur between the…

Q: Rank the following E2 reactions in order of increasing rate. Ph, OTs OTs NaOH NaOH ? NaNH, A Ph.…

A: E2 reaction is bimolecular elimination reaction. Rate = kRXBase, X is the leaving group Rate is…

Q: сн NaOCH,CH3 н CнCH2он heat

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Q: ö: Br: H,0 heat ОН DH

A:

Q: NAOH NH2 + NH, H2O

A: See mechanism below.

Q: The E2 Mechanism Draw the major and minor elimination products for the reaction of…

A:

Q: NaOH N2OCH3 H3CO OCH heat

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

Q: CH2- HI

A:

Q: Provide the complete arrow pushing mechanism and the major product for the foll 8) reaction. Major…

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

Q: EtO, Eto OMe OMe NH 6 py: ба Ph Ph

A: In this mechanism, lone pair electrons on the N atom is attacked to the carbonyl carbon. Finally HCl…

Q: Provide a reasonable mechanism for the following reaction. TMSO SnCl, OMe Meo OMe

A: Note : Ketal deprotection follows Sn1 mechanism. The generated carbocation is attacked by double…

Q: draw out a detailed mechanism showing the transformation from stilbene to stilbene dibromide C14H12…

A: The reaction taking place is given as, => C14H12 + 2 HBr + H2O2 -------> C14H12Br2 + 2 H2O

Q: Ph Na Oet Eto OEt

A:

Q: .CI AICI, 'CI 'CI

A: Ans  Electrophilic substitution reaction takes place

Q: + `NH,

A:

Q: NaOH H. H,O

A: The question is based on the concept of organic mechanism. we have to explain the mechanism of aldol…

Q: nothe Write a detailed mechanism for this transformation но. HCI HO H20 H

A: The given reaction is an hydrolysis of ether

Q: Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions…

A:

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: Which rearrangement product will form preferentially during the [1,2]-rearrangement of an R-group?…

A: The rearrangement product is stable if the intermediate carbocation formed is stable. We have to see…

Stoichiometry

Stoichiometry is a chemical division that evaluates the quantitative content of the chemical process with the help of the reacting molecules or products taking part in the reaction. The term “stoicheion” in “Stoichiometry”, is an old Greek term for "element" whereas “metron” means "measure".