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.
Chapter10: Organohalides
Section10.2: Preparing Alkyl Halides From Alkanes: Radical Halogenation
Problem 4P: Taking the relative reactivities of 1°, 2°, and 3° hydrogen atoms into account, what product(s)...
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The molecule above the arrow is NaOCH3
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