Provide the complete mechanism using Curved Arrow Formalism for the reaction of benzoic anhydride treated with the compound shown below. Tell which layer (aqueous or organic) the product(s) will be isolated in. *NH2

Q: You have learned two ways to make an alkyl benzene: Friedel–Craftsalkylation, and Friedel–Crafts…

A: Alkyl benzenes are the substituted benzene in which substituent is an alkyl group. Benzene undergoes…

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: 1)…

A: LiAlH4 acts as reducing agent.

Q: H E1 ČI

A: Here E1 elimination takes place . Since in E1 elimination carbocation intermediate is formed so…

Q: draw the electrophilic aromatic substitution (EAS) mechanism for the reaction with +NO2, water…

A: Electrophilic substitution of benzene derivatives: In electrophilic substitution of benzene, one of…

Q: Please draw a complete mechanism to account for the process shown below, including ALL resonance…

A: In the given reaction NaNO2 reacts with HCl to form NO+ which acts as an E+.

Q: Provide the curved-arrow mechanism to account for the following nucleophilic addition- elimination…

A: Nucleophile attacks on carbonyl carbon to produce tetrahedral intermediate. This tetrahedral…

Q: When the illustrated reagents are treated with a strong base the indicated reaction is observed to…

A: Witting reagent contains triphenyl as substituents and utilized in the generation of alkene. In the…

Q: Draw the complete, detailed mechanism for the addition of hexan-3-ol to dihydropyran and predict the…

A: The given reaction is,

Q: Propose a reasonable mechanism that would account for the reaction shown here. H2O HBr НО

A: Addition of strong acid such as HBr forms a carbocation in the reaction which is formed on a four…

Q: Predict the product of the reaction between acetic anhydride and each of the following compounds. If…

A: As here question has multiple subparts, so solve first three subparts. If student want complete…

Q: Give the major elimination product derived from each of the following elimination reactions. Pay…

A:

Q: Show the complete mechanism using Curved Arrow Formalism for the reaction of the compound shown…

A: INTRODUCTION: p-chlorobenzaldehyde reacts with EtOH and HCl to give an acetal.

Q: (e) When treated with base, the compound shown below cyclizes. Show the structure and relative…

A:

Q: CH3 NaOD/D20 CH

A: In the above reaction, we have reactant ketone with 1 acidic alpha H in it. And the reagents are…

Q: on to react with the ketone in the remainder of the mechanism. The reaction takes placCe under…

A:

Q: A student wanted to prepare (1-Ethylpropoxy)cyclopentane by heating cyclopentanol and pentan-3-ol…

A: The given structure is represented as follows:

Q: NaN N'

A: Nucleophilic addition- elimination reaction is a reaction in which the substitution of any group…

Q: omplete the following mechanism , show all steps and arrows in full

A: The Fries rearrangement reaction is an organic name reaction which involves the conversion of…

Q: Draw the complete mechanism you would expect for the reaction of tert. butyl bromide with sodium…

A: Tert. butyl bromide is bulkier group and when it's reacts with smaller stronger base then this base…

Q: (a) Draw the mechanism for the following transformation including reagents and any isolable species…

A:

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

A:

Q: heel HO он NaOH (a)

A:

Q: CH2CH3 H3CH2C- Br CH;OH 1) CH2CH3 CI H2Q 2) H3C-C- CH2CH3 (R) 3) CH;CH,CI NaOCH,CH3 CH3 4) NaOH…

A: SN1 Reactions: Nucleophilic substitution reactions, in which the tertiary or secondary alkyl halide…

Q: raw the structure of the alkene that would give only the following products upon ozonolysis followed…

A: The products of the ozonolysis reaction is given as,

Q: An enamine, R2C=C-NR2, behaves as a nucleophile in much the same way that an enolate anion does.…

A: Enolate ions have two or more reactive sites so they are called, ambident reactive species. The…

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

A: Alcohols undergo elimination reaction in the presence of acid to form an alkene as a product. The…

Q: When phenyl-5-bromopentanone is treated with triphenylphosphine, followed by base, a compound is…

A: The structure of triphenyl phosphine is

Q: For each sequence of reactions, draw the complete, detailed mechanism and predict the major organic…

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

Q: OTs - (strong base) В Doubling [B] doubles rate of rxn.

A: The reaction involves a carbocation intermediate and is commonly seen in reactions of secondary or…

Q: Provide a reasonable mechanism that provides the major product for the reaction scheme provided…

A: The reaction given is,

Q: Treatment of 1,2-dibromoethane with the dithiolate dianion shown in the reaction below leads to two…

A: 1st product C4H8S2

Q: Suggest a reasonable mechanism for the following reaction Ph OCH3 Ph. OCH3 FeCla Ph Ph OCH3

A: FeCl3 acts as a catalyst. It helps in removal of methoxy group to produce electrophile. Attack of…

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

A:

Q: When the depicted alkyne is treated first with sodium amide and then with the alkyl halide shown,…

A: We have given when  alkyne is treated first with sodium amide and then with the alkyl halide. It is…

Q: Explain how an El reaction that generates an alkene may be reversible under the reaction conditions…

A: Here we have to explain why E1 reaction is reversible under reaction conditions but E2 reaction is…

Q: HO H2SO4 H2O, heat

A: This reaction proceed through E1 mechanism And the product of this reaction is

Q: Provide the complete mechanism using curved arrow formalism for the reaction of pyruvic acid treated…

A:

Q: Write a plausible mechanism for this transformation. Only two sequential pericyclic reactions are…

A: In organic chemistry, pericyclic reactions are those in which the shifting of double bonds or…

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: Consider the following reaction. In the absence of peroxides, the major product of the reaction is…

A: Since we know that alkene react with HBr in absence of peroxide to form bromo-alkane by ionic…

Q: 3. Provide the complete mechanism for each of the following reaction. Н-Br

A: Provide the complete mechanism for each of the following reaction.

Q: Which of the following is the product of the reaction sequence below?

A:

Q: 1) NaH 2) 3) H*, heat

A: NaH (sodium hydride) is a strong base. It abstracts a proton from more acidic hydrogen. The…

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

A: Please find the attachment.

Q: The reaction of aniline with benzoyl chloride (an acid chloride) produces a mixture of two products,…

A:

Q: Treatment of but-2-yne with NCS affords an interesting molecule with two methoxy groups and two…

A:

Q: 1) NaOH H 2) H*, heat

A:

Q: Complete the mechanism for the acid-catalyzed alcoholysis of the epoxide by adding missing atoms,…

A: The two major steps in the reaction are protonation of epoxide and attack of nucleophile at the most…

UV Visible Spectroscopy

Spectroscopy refers to the absorption or emission of light or other radiations by matter. When a substance or chemical absorbs light or radiation, they reach an excited state followed by de-excitation or emission of the light or radiation forming distinct spectra. UV-visible spectroscopy or  ultraviolet-visible refers to the absorption and emission in the ultraviolet and visible regions of the electromagnetic spectrum.