V. @Given the followingmechanism fer meYOCHSNaOHreaction show the detailedconversion of A to B•OCN3CH3OH.OH(A)(B)cⒸ using the same detailed mechanism instead ofcyclonexare ring as shown in product. B, proposeandfer a product wila cyclopentane ning instead of a cyclohexane viny.Ⓒ Exploumpand I withwhy campand (B) is preferred over thecampanay campandwith a cyclopentake ring..

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V. @Given the following reaction mechanism fer me conversion Y OCHS. NaOH CH3OH. (B) show the detailed of A to B •OCN3 OH (A) c Ⓒ using the same detailed mechanism, instead of cyclonexare ring as shown in product. B, and fer a product wil ning instead of a cyclohexane ving. propose a cyclopentane Ⓒ Explumpandy with why campand (B) is preferred over the campanay cumpand with a cyclopentake ring..

V. @Given the following reaction mechanism fer me conversion Y OCHS. NaOH CH3OH. (B) show the detailed of A to B •OCN3 OH (A) c Ⓒ using the same detailed mechanism, instead of cyclonexare ring as shown in product. B, and fer a product wil ning instead of a cyclohexane ving. propose a cyclopentane Ⓒ Explumpandy with why campand (B) is preferred over the campanay cumpand with a cyclopentake ring..

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter23: Carbonyl Condensation Reactions

Section23.SE: Something Extra

Problem 42MP

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