Naproxen, sold under the brand name Aleve among others, is a nonsteroidal anti- inflammatory drug (NSAID) used to treat pain (e.g. menstrual pains), inflammatory diseases such as rheumatoid arthritis, and fever. It is taken orally. The most potent enantiomer (the (S)-enantiomer) is produced by an asymmetric catalytic hydrogenation using Noyori's BINAP- ligand and ruthenium: CH3 COOH H2. [Ru(OAc),BINAP] coOOH MeO Meo (S)-Naproxen, 97% ee PPh PPH2 (R)-BINAP (i): After the reaction has completed analysis shows that the reaction mixture contains 392 g of (S)-naproxen (Mw 230,26 g/mol). How much of the (R)-enantiomer is expected to have been formed when the enantiomeric excess is 97% for the reaction? (ii): Explain briefly why the %enantiomeric excess can be regarded as a key green metric.
Naproxen, sold under the brand name Aleve among others, is a nonsteroidal anti- inflammatory drug (NSAID) used to treat pain (e.g. menstrual pains), inflammatory diseases such as rheumatoid arthritis, and fever. It is taken orally. The most potent enantiomer (the (S)-enantiomer) is produced by an asymmetric catalytic hydrogenation using Noyori's BINAP- ligand and ruthenium: CH3 COOH H2. [Ru(OAc),BINAP] coOOH MeO Meo (S)-Naproxen, 97% ee PPh PPH2 (R)-BINAP (i): After the reaction has completed analysis shows that the reaction mixture contains 392 g of (S)-naproxen (Mw 230,26 g/mol). How much of the (R)-enantiomer is expected to have been formed when the enantiomeric excess is 97% for the reaction? (ii): Explain briefly why the %enantiomeric excess can be regarded as a key green metric.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question
4
![(A):
Naproxen, sold under the brand name Aleve among others, is a nonsteroidal anti-
inflammatory drug (NSAID) used to treat pain (e.g. menstrual pains), inflammatory diseases
such as rheumatoid arthritis, and fever. It is taken orally. The most potent enantiomer (the
(S)-enantiomer) is produced by an asymmetric catalytic hydrogenation using Noyori's BINAP-
ligand and ruthenium:
CH3
Ha Ru(OAc),BINAP)
COOH
COOH
Meo
Meo
PPH2
(S)-Naproxen, 97% 00
PPH2
(R)-BINAP
(i): After the reaction has completed analysis shows that the reaction mixture contains 392 g
of (S)-naproxen (Mw = 230,26 g/mol). How much of the (R)-enantiomer is expected to have
been formed when the enantiomeric excess is 97% for the reaction?
(ii): Explain briefly why the %enantiomeric excess can be regarded as a key green metric.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd45b7e38-406f-4a21-8154-727a144708f4%2Fbe31b1d6-8a81-4e84-af86-9cdc1b5f3d17%2Fjpu05ox_processed.jpeg&w=3840&q=75)
Transcribed Image Text:(A):
Naproxen, sold under the brand name Aleve among others, is a nonsteroidal anti-
inflammatory drug (NSAID) used to treat pain (e.g. menstrual pains), inflammatory diseases
such as rheumatoid arthritis, and fever. It is taken orally. The most potent enantiomer (the
(S)-enantiomer) is produced by an asymmetric catalytic hydrogenation using Noyori's BINAP-
ligand and ruthenium:
CH3
Ha Ru(OAc),BINAP)
COOH
COOH
Meo
Meo
PPH2
(S)-Naproxen, 97% 00
PPH2
(R)-BINAP
(i): After the reaction has completed analysis shows that the reaction mixture contains 392 g
of (S)-naproxen (Mw = 230,26 g/mol). How much of the (R)-enantiomer is expected to have
been formed when the enantiomeric excess is 97% for the reaction?
(ii): Explain briefly why the %enantiomeric excess can be regarded as a key green metric.
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