Your Name: 1. (a) Discuss with your group why each transformation (A, B, and C) shown below will not produce the product shown. Be sure to include any applicable discussion on choices of reagents, regioselectivity and stereochemical outcome expected versus what is shown in the product. Your peer review for other students should include discussion about why you agree or disagree with the others' responses. Don't just simply comment "I agree” or I disagree”. Discuss helpful and insightful suggestions for responses you don't agree with. You should all come to a general consensus of why each case will not work as originally shown. (b) Propose a way to fix the conditions so that the desired product provided can be made from the substrate given. You can do this simply by constructing a new scheme. Be sure to show the correct reagents/conditions for each step and make sure that each step is in the correct order. If applicable, the proposed "fix" should also consider both the regio- and stereochemistry shown in the desired product. There may be more steps required than the number originally shown for each transformation. You will need to recall knowledge of both current and previous reactions presented in the course and text book. In your peer review, discuss why you think each proposed correction will or will not work. Offer insightful suggestion for improvement in such cases. You should all come to a general consensus of a proposed route that will work. reagents/ conditions A. OH 1. OsO4, H₂O 2. NaSH + enantiomer "SH substrate desired product

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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Your Name:
1. (a) Discuss with your group why each transformation (A, B, and C) shown below will not
produce the product shown. Be sure to include any applicable discussion on choices of reagents,
regioselectivity and stereochemical outcome expected versus what is shown in the product.
Your peer review for other students should include discussion about why you agree or disagree
with the others' responses. Don't just simply comment "I agree” or I disagree”. Discuss helpful
and insightful suggestions for responses you don't agree with. You should all come to a general
consensus of why each case will not work as originally shown.
(b) Propose a way to fix the conditions so that the desired product provided can be made from the
substrate given. You can do this simply by constructing a new scheme. Be sure to show the correct
reagents/conditions for each step and make sure that each step is in the correct order. If applicable,
the proposed "fix" should also consider both the regio- and stereochemistry shown in the desired
product. There may be more steps required than the number originally shown for each
transformation. You will need to recall knowledge of both current and previous reactions
presented in the course and text book.
In your peer review, discuss why you think each proposed correction will or will not work. Offer
insightful suggestion for improvement in such cases. You should all come to a general consensus
of a proposed route that will work.
reagents/
conditions
A.
OH
1. OsO4, H₂O
2. NaSH
+ enantiomer
"SH
substrate
desired product
Transcribed Image Text:Your Name: 1. (a) Discuss with your group why each transformation (A, B, and C) shown below will not produce the product shown. Be sure to include any applicable discussion on choices of reagents, regioselectivity and stereochemical outcome expected versus what is shown in the product. Your peer review for other students should include discussion about why you agree or disagree with the others' responses. Don't just simply comment "I agree” or I disagree”. Discuss helpful and insightful suggestions for responses you don't agree with. You should all come to a general consensus of why each case will not work as originally shown. (b) Propose a way to fix the conditions so that the desired product provided can be made from the substrate given. You can do this simply by constructing a new scheme. Be sure to show the correct reagents/conditions for each step and make sure that each step is in the correct order. If applicable, the proposed "fix" should also consider both the regio- and stereochemistry shown in the desired product. There may be more steps required than the number originally shown for each transformation. You will need to recall knowledge of both current and previous reactions presented in the course and text book. In your peer review, discuss why you think each proposed correction will or will not work. Offer insightful suggestion for improvement in such cases. You should all come to a general consensus of a proposed route that will work. reagents/ conditions A. OH 1. OsO4, H₂O 2. NaSH + enantiomer "SH substrate desired product
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