15) There are two parts to this question (a & b), be sure to answer both. (a) frs) When (R)-alkyl halide shown is allowed to react with CH3S-Nat, an optically active product is formed in high yield. Draw this product(be sure to show/write stereochemistry). HERE HSCH₂C Br (b (R) H₂C H Optically active alkyl halide +CH,SNat Acetone www.w (5) SCHE Optically active product s) For the reaction in part (a), show a mechanism for the formation of the products that

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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15) There are two parts to this question (a & b), be sure to answer both.
(a) frs) When (R)-alkyl halide shown is allowed to react with CH3S-Nat, an optically active
product is formed in high yield. Draw this product(be sure to show/write stereochemistry).
KELEN
H₂CH₂C
Br
(b)
you arew.
(R)
H
H₂C
Optically active alkyl halide
+CH,SNa
Acetone
340-SONG
Optically active product
3) For the reaction in part (a), show a mechanism for the formation of the products that
Transcribed Image Text:15) There are two parts to this question (a & b), be sure to answer both. (a) frs) When (R)-alkyl halide shown is allowed to react with CH3S-Nat, an optically active product is formed in high yield. Draw this product(be sure to show/write stereochemistry). KELEN H₂CH₂C Br (b) you arew. (R) H H₂C Optically active alkyl halide +CH,SNa Acetone 340-SONG Optically active product 3) For the reaction in part (a), show a mechanism for the formation of the products that
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