8-8-8 Regioslective Hydrolysis Raney Ni Direct Hydrogenation + HCI 2) Na₂CO₂ NH₂ Hydrolysis COOH

Q: In electrophilic aromatic substitution reaction by drawing the structures of the compounds given…

A: Electrophilic aromatic substitution :- Electrophilic aromatic substitution simply means attack of…

Q: Write a reaction scheme and draw the reaction mechanism for the williamson ether synthesis.

A: The Williamson ether synthesis is an organic reaction in which the forming an ether from an…

Q: Complete the reaction below. 1) What are the names of the starting compound and product? 2) Draw out…

A: The given reaction is an acid catalysed lactone formation reaction from a hydroxy carboxylic acid.…

Q: Provide a reasonable arrow pushing mechanism for the following reaction: OH NaOH

A: At first base abstract alcoholic proton and form alkoxide,then negative charge is back and…

Q: Draw a general Mechanism for Electrophillic Aromatic Substitution (EAS) reaction

A:

Q: In electrophilic aromatic substitution, a group attached to the aromatic ring does not affect ring…

A: In electrophilic aromatic substitution(EAS) reaction, an electron-deficient species    (i.e…

Q: 4. Device the synthesis of the following molecules starting from the given precursor. a) b)…

A: 1) The reagents CH3Cl/AlCl3 will convert benzene to toluene then radical bromination will produce…

Q: Previde a curved arrow mechanism for the following reaction. NaCl

A:

Q: HI (excess)

A: While writing the mechanism use electron pushing arrow from electron rich center to electron poor…

Q: ㅅ *Br:

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Why alkyl groups considered as an ortho- , para-directing?

A: To find: Why alkyl groups are considered as an ortho-, para-direction

Q: 2. Draw a curved arrow mechanism for each of the following reactions. KOH heat H₂O S H₂O KOH (cat.)

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: (SYN) For each compound in Problem 23.49, determine whether fuming sulfuric acid should be added to…

A: (a)

Q: да H₂SO4 H2O НО. 9₂H Н + ОН

A:

Q: H,0 HCI ()

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

Q: H2SO4 (cat) МеОН (solvent) HS. ОН

A: Step 1: Hemi acetal formation. Step 2: Hemi acetal is attacked by double bond results carbocation.…

Q: Draw the appropriate reagents/ solvent

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: Select the keyword or phrase that will best complete each sentence. Key terms: backside carbocation…

A: SN1 :- unimolecular nucleophilic substitution reaction. It is two step reaction involes formation of…

Q: D July 애 H Drodunt

A: Debromination gives primary carbocation. Now, elimination of proton gives product.

Q: + HO Br

A:

Q: (b) Show how to synthesize the molecule at right, using the molecule at left as a carbon source,…

A: The addition of an enolate ion to an alpha-beta unsaturated carbonyl compound is called a conjugate…

Q: Select the bond that must break when these electrons flow as shown by the mechanistic arrow

A: Water is amphoteric in nature it act as acid as well as base. It can donate proton as well as it…

Q: Foresee the resulting products from exciting the given molecule and determine which product is…

A: The objective of this question is to predict the resulting products from exciting the given molecule…

Q: Choose the best reagents to complete the reaction shown below.

A:

Q: Answer in  not more than 5 sentences Discuss how to use a desiccator. When should a desiccant be…

A: Dessicator is sizable enclosure which is used for chemicals which are hygroscopic in nature.

Q: Please be certain to use good curved arrow notation for your mechanism. HYH2O HO,

A:

Q: Draw a mechanism for the reaction below. CHỊNH, dan CHÍNH,

A: We have find out the product of given reaction.

Q: C.) Obtain oxidation reduction products in four different ways using benzaldehyde and appropriate…

A: Solution- Oxidation reactions of benzaldehyde : 1. 2.

Q: provide synthesis. Use benzene and any reagents four carbona or leasa

A: The objective of the question is to provide a synthesis using benzene and any reagents with four…

Q: Please kindly provide the curved arrow mechanism for the conversion of the starting material to the…

A: These tye of questions are done using carbocationic rearrangements. Driving force for the reactions…

Q: NaOH

A: The base will first abstract the proton from alpha carbon of the carbonyl, and it forms an enolate…

Q: When the alkene below reacts with Hg(OAc)2, two mercurinium ions form in equal amounts. Draw both…

A: The given question contains various reactions of alkenes. The reactions are explained below-

Q: 2C.) Provide missing reagent(s) in the box. Br OH

A: For a Diels-Alder reaction to occur the diene should be in s-cis conformation

Q: Complete the following nucleophilic addition reactions: Part A __ CH3–CH2–CH2CH + CH CHOH H+

A: In the above reaction an aldehyde and alcohol is treated in the presence of H+ (acid). This will…

Q: How the synthesis is conceptually divided ?

A: A sound knowledge of mechanistic organic chemistry, detailed information on the art and science of…

Q: Complete the mechanism for the resonance stabilization. Draw the curved arrows, and complete the…

A: The objective of this question is to elucidate the resonance stabilization in the transformation of…

Q: 2. Please complete the following reaction and draw a step wise mechanism. A1C13

A: Friedel-Crafts alkylation reaction is an organic coupling reaction that replaces an aromatic proton…

Q: What acetylide anion and alkyl halide can be used to prepare attached alkyne? Indicate all…

A: The given alkyne hept-2-yne can be prepared through 2 routes.

Q: Give a clear handwritten answer with explanation..give the mechanism with explanation of given bleow…

A: In this question, we will see the reaction mechanism for the given transformation from the reactant…

Q: 10. Draw a complete curved arrow mechanism for the following reaction sequence. CC13H + KOt-Bu +

A: CCl2 carbene formation take place Carbene insert into alkene below the plane Explanation:

Q: Complete the following synthesis. Show all intermediate products, and reagents. x-α

A: Solution: Organic synthesis is a most interesting topic in which we must have knowledge about some…

Q: Show all the arrow mechanism including the PROPER reagents.

A:

Q: Explain why substitution is difficult on accomplish on the benzene ring?

A: Benzene is a planar molecule having delocalized electrons above and below the plane of ring. Hence,…

Q: Draw generic mechanism for SN2 & SN1 reactions

A: We have to give the generic mechanisms for Sn1 and Sn2 reaction.

Q: де + HOCH₂CH₂OH HCI он +

A: