V. @Given the following reaction shall the detailed 1 mechanism fer me Conversion of A to B •OCN3 y OCH3 Na och 3 CH 3 OH. (B) OH (A) Ⓒ using the same detailed mechanism, instead of a cyclonexare ving as shown in product B, propuse a structure and mechanism fer a product wil 1.d. cyclopentane ning instead of a cyclohexane ving. Ⓒ Explcompund with why campandy. campand campand (B) is preferred over the a cyclopentare ring.

V. @Given the following reaction shall the detailed 1 mechanism fer me Conversion of A to B •OCN3 y OCH3 Na och 3 CH 3 OH. (B) OH (A) Ⓒ using the same detailed mechanism, instead of a cyclonexare ving as shown in product B, propuse a structure and mechanism fer a product wil 1.d. cyclopentane ning instead of a cyclohexane ving. Ⓒ Explcompund with why campandy. campand campand (B) is preferred over the a cyclopentare ring.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.2: Preparing Alkyl Halides From Alkanes: Radical Halogenation

Problem 4P: Taking the relative reactivities of 1Â°, 2Â°, and 3Â° hydrogen atoms into account, what product(s)...

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V. @Given the following mechanism fer me Y OCHS NaOH reaction show the detailed conversion of A to B •OCN3 CH3OH. OH (A) (B) c Ⓒ using the same detailed mechanism instead of cyclonexare ring as shown in product. B, propose and fer a product wil a cyclopentane ning instead of a cyclohexane viny. Ⓒ Exploumpand I with why campand (B) is preferred over the campanay campand with a cyclopentake ring..
V. @Given the following reaction show the detailed mechanism fer me 1 Conversion of A tu B •OCN3 OYOCH'S (A) Na och 3 CH3OH. almost the Ⓒ detailed using the identical. cyclonexare ving as a structure and .d. cyclopentane ning instead (B) OH а mechanism, instead of shoaln in product B, propase mechanism fer a product W/ a cyclohexane ving.
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