Make an electron-flow-mechanism for this synthetic scheme. This involves predicting major and by. products using electronic and structural effects. The arrow push mechanism must be shown. (4-bromo-3- nitroacetophenone to flurbiprofen) with label

Q: C NasH Hgot

A:

Q: Provide the Cruved arrow mechanism of anisole treated with bromine with iron (III) bromide. Include…

A: Here we are required to predict the mechanism of anisole with bromine with FeBr3.

Q: Explain in details the mechanism of preparing B-ionone from first step till last step. Please write…

A: Applying concept of organic synthesis and reagent.

Q: Give the mechanasim Br₂ ccty HBr H₂02 НВО C

A: Reaction 1 : Br2 addition to alkenes produces trans -1,2-dibromo compound. Reaction 2 : HBr addition…

Q: Provide the best retrosynthesis nantanol an ner

A:

Q: enzoate. The nitro substituent was introduced in the meta position of the methy Why does it…

A: It is due to the -R effect of the COCH3 gruop, a positive charge will be generated at the ortho- and…

Q: Please

A: We will write all the intermidiate

Q: Outline (not mechanism) all steps in the laboratory synthesis of the following from benzene and/or…

A: Interpretation -  To outline the all steps in the laboratory synthesis of the following from benzene…

Q: (A) Provide the major organic product for the reaction below (B) Would the product be optically…

A: Sugar undergoes oxidation reaction in presence of HNO3 . Both aldehyde and alcohol group is oxidis

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

A: The given reactant is a tertiary alkyl bromide which is an alkyl halide.  The reagent is KCN and the…

Q: Compare Electrophilic aromatic substitution reactivity to quinoline and isoquinoline. Please,…

A: Quinoline/isoquinoline - attack at 5,8 benzene positions 5 membered rings - electron rich, readily…

Q: Provide a note on Peterson syntheses, with suitable example and mechanism.

A: Peterson synthesis is synthesis of olefinic double bond from carbonyl using α-silyl alkane.

Q: The -NH, group is listed in our textbook as the strongest o,p-directing activator in electrophilic…

A: Given :

Q: OH Br NBS NaOH Acetone/H,O limonene bromohydrine limonene oxide

A:

Q: b) Visualise following instructed) (i) the retrosynthesis for the target compounds (as along with…

A:

Q: Draw the mechanism with curved arrows (Williamson Ether Synthesis). Please provide detailed…

A: Williamson synthesized the ether from alcohol

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

A: Nucleophilic substitution reaction is an organic reaction in which a nucleophile replaces another…

Q: Give the reagents and results/observation

A: NaHSO3 test : This is a characteristic test for carbonyl compounds. This test is given by small…

Q: Pentalene is most elusive molecule and has never been isolated. The pentalene dianion, however, is…

A: Aromatic Compounds are the compounds which are planar, cyclic, conjugation of π electrons and has to…

Q: TsO, Et,N: DMSO

A: Removal of OTs gives a carbocation which undergoes ring expansion via alkyl shift to produce another…

Q: Provide mechanism with curved arrows for Part B: Synthesis of benzil

A: PhC(=O)-CH(IH)-Ph on oxidation with HNO3 gives Ph-C(=O)-C(=O)-Ph which is called benzil.  At first…

Q: Give any reaction to show asymmetric synthesis.

A: Asymmetric synthesis. A  particular synthesis where a new chiral centre is created in an optically…

Q: Outline

A:

Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…

A: Ring opening reactions for A and B are given below :

Q: Design a reasonable synthesis for the following transformation. + C.

A:

Q: provide CLEAR AND NEAT mechanism with curved arrows for  Part A: Synthesis of benzoin

A: At first HO^- abstract the most active hydrogen from thiamine hydrochloride to get nucleophilic…

Q: Provide necessary carbonyl compound and phosphonium ylide to yield the alkene. What type of ylide…

A: Given,

Q: Please provide complete explanation. Thank you! Is recrystallization necessary in synthesizing…

A: Interpretation- We have to tell that , Is recrystallization is necessary  in synthesizing…

Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…

A:

Q: reasonable synthesis? might need to use both grignard and a gilman reagent (organocuprate)

A: Synthesis of product by using Gilmann and Grignard reagent.

Q: Perform a retrosynthetic analysis (please include - disconnection etc) and suggest a synthesis of…

A: The retrosynthesis method is used to determine the starting material by the fragmentation of the…

Q: Please provide a synthetic approach for the following reactions. Make sure to do the retrosynthetic…

A:

Q: Provide only one plausible retro synthetic scheme for the molecule below. In addition, provide a…

A:

Q: Can you please send me the answers for d) and e) attached.  Thanks. Are the following molecules…

A: Molecules are defined as the chiral molecules if the mirror image of the molecule is cannot be…

Q: The follow ing compound can be synthesized by a mixed Claisen condensation. Identify the two…

A: Claisen condensation reaction is a reaction between two esters in presence of strong base to form…

Q: Propose a stepwise mechanism for this reaction. The bicarbonate ion will act as a base in the…

A: The given reaction is,

Q: Provide a retrosynthetic analysis and forward synthesis for the compound shown below. and any other…

A:

Q: Provide mechanism (arrow pushing) for this Friedel Crafts alkylation, include electrophile and…

A:

Q: Outline the mechanism for the conversion of benzene to methylbenzene

A: The mechanism for conversion of benzene to methylbenzene is shown in the image below.

Q: Please explain benzyne mechanism?

A: Nucleophilic aromatic substitution reactions are not easy to carry out. As benzenes rings are…

Q: Provide mechanism with curved arrows for Part C: Synthesis of tetraphenylcyclopentadienone

A:

Q: A problem in dyeing fabrics is the degree of fastness of the dye to the fabric. Many of the early…

A: When a nucleophile displaces a leaving group from an aromatic system, then the reaction is termed as…

Q: In an essay provide written explanation, In Sunthesis of Diben zalacetone, why does the reaction end…

A: Dibenzalacetone is synthesized by using two moles of benzaldehyde with acetone in the presence of…

Q: Using curved arrows to show the flow of electrons, and being careful to balance mass and charge for…

A: Given : reaction

Q: Provide a curved arrow mechanism for the SN1 reaction below: CI CH3 H,C NACN

A: SN1 is a unimolecular nucleophilic substitution reaction. A carbocation is formed after the eviction…

Q: CN

A: The conversion involves reaction of aldehyde with grignard reagent followed by substitution reaction…

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: The plausible arrow pushing reaction mechanism is provided below in attach image .

Q: Provide the curved arrow mechanism of m-xylene treated with isopropylchloride with iron (III)…

A: