please DRAW the carbene mechanism for the formation of this five membered ring. Please Draw. H3CO2C H3CO₂C Me toluene, reflux OMe Me ✗ N=N OMe
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A: Please refer below page.If you have any doubts please feel free to ask.Explanation:Step 1: Step 2:…
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- The following chiral compound undergoes a stereospecific E2 reaction, where only one stereoisomer is produced as product. What is the product of the reaction?Provide the E2 mechanism for the di-dehydrobromination of (meso)-stilbene dibromideBetween E1 and E2, which reaction mechanism is most efficient to synthesize the (E) stereoisomer of this product on an industrial scale?
- Azo coupling reaction. Provide a mechanism with intermediates and arrowsIdentify which substitution mechanism best fits the following statement: The reaction proceeds through a concerted mechanism. A) SN1 B) SN2Which of the following ff. halides is most likely to react through the SN1 mechanism? i. CH3Clii. CH2=CHCH2CH2Cliii. CH3CH=CHCH2Cl iv. CH2=CHCl
- Between E1 and E2, which reaction mechanism is more efficient to synthesize the (E) stereoisomer of this product on a large scale?Decide on the mechanism for each substitution, and then pick the solvent that affords the faster reaction. a.(CH3CH2)2CClCH3 + CH3OH in CH3OH or DMSO b.CH3CH2CH2Br + −OH in H2O or c. DMF (CH3CH2)2CHCl + CH3O− in CH3OH or HMPADraw curved arrows to illustrate the mechanism for the reaction of 3‑methylbutan‑1‑ol and HBrHBr. The starting material and intermediates have been pre‑drawn for your convenience.
- Ring opening reaction of tetrahydrofuran catalyzed by basic materialsThe dehydration of 1-phenylcyclohexanol with sulfuric acid follows an E1 pathway. What produces the substantial stability of the intermediate carbocation? Please explain using pictures and words.In an experiment, E,E-2,4-hexadien-1-ol is heated with malic anhydride to produce a bicyclic lactone. Propose a mechanism for the formation of the product, including the structure of the intermediate 4+2 adduct. The image of this reaction is attached.
