When oxaloacetic acid and acetyl-coenzyme A (acetyl-CoA) labeled with radioactive carbon-14 in position 2 are incubated with citrate synthase, an enzyme of the tricarboxylic acid cycle, only the following enantiomer of [2-14C]citric acid is formed stereoselectively. Note that citric acid containing only 12C is achiral. Assign an R or S configuration to this enantiomer of [2-14C]citric acid. (Note: Carbon-14 has a higher priority than carbon-12.) C-COOH 14CH,COOH citrate synthase ČH,COOH + 14CH,CSCOA НООС -COH CH,COOH Oxaloacetic acid Acetyl-CoA [2-14C]Citric acid
When oxaloacetic acid and acetyl-coenzyme A (acetyl-CoA) labeled with radioactive carbon-14 in position 2 are incubated with citrate synthase, an enzyme of the tricarboxylic acid cycle, only the following enantiomer of [2-14C]citric acid is formed stereoselectively. Note that citric acid containing only 12C is achiral. Assign an R or S configuration to this enantiomer of [2-14C]citric acid. (Note: Carbon-14 has a higher priority than carbon-12.) C-COOH 14CH,COOH citrate synthase ČH,COOH + 14CH,CSCOA НООС -COH CH,COOH Oxaloacetic acid Acetyl-CoA [2-14C]Citric acid
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...
Related questions
Question
![When oxaloacetic acid and acetyl-coenzyme A (acetyl-CoA) labeled with radioactive
carbon-14 in position 2 are incubated with citrate synthase, an enzyme of the tricarboxylic
acid cycle, only the following enantiomer of [2-14C]citric acid is formed stereoselectively.
Note that citric acid containing only 12C is achiral. Assign an R or S configuration to this
enantiomer of [2-14C]citric acid. (Note: Carbon-14 has a higher priority than carbon-12.)
C-COOH
14CH,COOH
citrate
synthase
ČH,COOH + 14CH,CSCOA
НООС
-COH
CH,COOH
Oxaloacetic acid
Acetyl-CoA
[2-14C]Citric acid](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F87a42ae5-c820-4a8e-a772-eb6b3eb32e94%2Ffc09ddc1-b20a-4d0a-82de-da2c87df4a36%2Faopozon.jpeg&w=3840&q=75)
Transcribed Image Text:When oxaloacetic acid and acetyl-coenzyme A (acetyl-CoA) labeled with radioactive
carbon-14 in position 2 are incubated with citrate synthase, an enzyme of the tricarboxylic
acid cycle, only the following enantiomer of [2-14C]citric acid is formed stereoselectively.
Note that citric acid containing only 12C is achiral. Assign an R or S configuration to this
enantiomer of [2-14C]citric acid. (Note: Carbon-14 has a higher priority than carbon-12.)
C-COOH
14CH,COOH
citrate
synthase
ČH,COOH + 14CH,CSCOA
НООС
-COH
CH,COOH
Oxaloacetic acid
Acetyl-CoA
[2-14C]Citric acid
Expert Solution

This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution!
Trending now
This is a popular solution!
Step by step
Solved in 2 steps with 8 images

Recommended textbooks for you

Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning

Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning

Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning

Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning

Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning

Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY