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

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.39P: Following are diastereomers (A) and (B) of 3-bromo-3,4-dimethylhexane. On treatment with sodium...

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