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Suffolk County Community College Ammerman Campus NAME: Due Thursday, 4/18 @ 12:30 PM (22 p 1. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook, propose a synthesis of the target molecule from the suggested starting materials (7 pts) Br NO₂ 2. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook propose a synthesis of the target molecule from the suggested starting materials. Hint your synthesis will require the use of a protecting group, either a cyclic acetal or a TBDMS ether. (7 pts) OH OH =0·50° (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required complete the transformations. Continue your answer on the back of this page, if necessary. (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required to complete the transformations. Continue your answer on the back of this page, if necessary

Suffolk County Community College Ammerman Campus NAME: Due Thursday, 4/18 @ 12:30 PM (22 p 1. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook, propose a synthesis of the target molecule from the suggested starting materials (7 pts) Br NO₂ 2. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook propose a synthesis of the target molecule from the suggested starting materials. Hint your synthesis will require the use of a protecting group, either a cyclic acetal or a TBDMS ether. (7 pts) OH OH =0·50° (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required complete the transformations. Continue your answer on the back of this page, if necessary. (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required to complete the transformations. Continue your answer on the back of this page, if necessary

Chemistry
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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Suffolk County Community College Ammerman Campus NAME: Due Thursday, 4/18 @ 12:30 PM (22 p 1. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook, propose a synthesis of the target molecule from the suggested starting materials (7 pts) Br NO₂ 2. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook propose a synthesis of the target molecule from the suggested starting materials. Hint your synthesis will require the use of a protecting group, either a cyclic acetal or a TBDMS ether. (7 pts) OH OH =0·50° (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required complete the transformations. Continue your answer on the back of this page, if necessary. (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required to complete the transformations. Continue your answer on the back of this page, if necessary
Transcribed Image Text:Suffolk County Community College Ammerman Campus NAME: Due Thursday, 4/18 @ 12:30 PM (22 p 1. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook, propose a synthesis of the target molecule from the suggested starting materials (7 pts) Br NO₂ 2. (a) Using retrosynthetic analysis and your knowledge of the reactions in chapters 7-19 of our textbook propose a synthesis of the target molecule from the suggested starting materials. Hint your synthesis will require the use of a protecting group, either a cyclic acetal or a TBDMS ether. (7 pts) OH OH =0·50° (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required complete the transformations. Continue your answer on the back of this page, if necessary. (b) Now rewrite the reactions in the forward direction. Include all organic and inorganic reagents required to complete the transformations. Continue your answer on the back of this page, if necessary
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