**Learning Target 6****Criteria for satisfactory score**All chirality centers must be correctly identified. All molecular drawings must be valid Lewis structures (octet rule, formal charge, valence, geometry). Definitions and explanations must be complete and logical. The process of the assignment of absolute configuration of a chirality center must be presented, not only the answer, with commentary where necessary.**Tasks**Compound 6 (Figure 3) shows the structure of an anticoagulant medication and a direct factor Xa inhibitor.1. Assign absolute stereochemistry of the chirality center that is shown (dash bond).2. Highlight all remaining chirality centers.3. Draw an example of two molecules that are regioisomers.![Compound 6, an anticoagulant drug, has a complex chemical structure featuring multiple rings and functional groups, labeled as compound 6.](compound6.png)*Figure 3: This drug generated $1.4 billion in sales in 2020.*

When carbon is bonded to four different groups/substituents, then the carbon can be termed as the…

Learning Target 6 Criteria for satisfactory score All chirality centers must be correctly identified. All molecular drawings must be valid Lewis structures (octet rule, for- mal charge, valence, geometry). Definitions and explanations must be complete and logical. The process of the assign- ment of absolute configuration of a chirality center must be presented, not only the answer, with commentary where necessary. Tasks Compound 6 (Figure 3) shows structure of an anticoagulant medication and a direct factor Xa inhibitor. 1. Assign absolute stereochemistry of the chirality center that is shown (dash bond) 2. Highlight all remaining chirality centers. 3. Draw an example of two molecules that are regioisomers. Ο ΗΝ HN- CI compound 6 Figure 3: This drug generated $1.4 billion in sales in 2020.

Learning Target 6 Criteria for satisfactory score All chirality centers must be correctly identified. All molecular drawings must be valid Lewis structures (octet rule, for- mal charge, valence, geometry). Definitions and explanations must be complete and logical. The process of the assign- ment of absolute configuration of a chirality center must be presented, not only the answer, with commentary where necessary. Tasks Compound 6 (Figure 3) shows structure of an anticoagulant medication and a direct factor Xa inhibitor. 1. Assign absolute stereochemistry of the chirality center that is shown (dash bond) 2. Highlight all remaining chirality centers. 3. Draw an example of two molecules that are regioisomers. Ο ΗΝ HN- CI compound 6 Figure 3: This drug generated $1.4 billion in sales in 2020.

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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as far as i know all the chiral molecule can be used to carry out optical resolution. so i think material C also can be an option but the answer says only E can be used. could you explain why not C? Please answer very soon will give rating surely
Please answer fully and showcase answer clearly for each part of the question this is only one questions I could really use your help with this
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hich molecules are diastereomers?
Please explain answers and include work. Please write the explanations and work out (do not type) so I can easily follow.
Identify the configuration of each chiral center in the following compound: 11, 12 10 14 which 4 13 In the boxes below, first input the number(s) corresponding to the chiral center(s) in numerical order as a comma separated list with no spaces (e.g., "1,3,4"). Then input the configuration(s) of the chiral center(s) in the same order and format (e.g., "R,S,S"). chiral center location(s): 2,5 Configuration(s):
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Your answer is partially correct. Identify the configuration of each chiral center in the following compound: Me eTextbook and Media H- Hint HỖ. Me OH In the boxes below, first input the number(s) corresponding to the chiral center(s) in numerical order as a comma separated list with no spaces (e.g., "1,3,4"). Then input the configuration(s) of the chiral center(s) in the same order and format (e.g., "R,S,S"). chiral center location(s): 3,6 Configuration(s): S.R H Assistance Used Assistance Used Attempts: 3 of 3 used
1. Make a qualitative plot of 4-ethyl-2-methylhexane showing the energy changes that arise from a 360° rotation about the C3-C4 bond. You do not need the actual numerical values of the energy changes, but you should label all maxima and minima with the appropriate Newman projections.