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OH NH₂ (1 eq.)

OH NH₂ (1 eq.)

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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The image displays two chemical reactions characterized by structural formulas and reagents. 1. **Reaction 1:** - **Reactant:** An ester with a tert-butyl group connected to a carbonyl, followed by a linear carbon chain ending in a hydroxyl group. This is often a compound like a protected alcohol. - **Reagent:** Pyridine, represented by a hexagonal ring with a nitrogen atom. - **Arrow:** Indicates progression of the reaction. 2. **Reaction 2:** - **Reactant:** A cyclic anhydride, depicted as a six-membered ring with two carbonyl groups at opposite positions. - **Reagent:** Amino-propene (specifically an allylamine), with a (1 eq.) notation, indicating the use of one equivalent. - **Arrow:** Indicates progression of the reaction. These reactions often involve protection and deprotection steps or attaching functional groups for synthesis in organic chemistry.
Transcribed Image Text:The image displays two chemical reactions characterized by structural formulas and reagents. 1. **Reaction 1:** - **Reactant:** An ester with a tert-butyl group connected to a carbonyl, followed by a linear carbon chain ending in a hydroxyl group. This is often a compound like a protected alcohol. - **Reagent:** Pyridine, represented by a hexagonal ring with a nitrogen atom. - **Arrow:** Indicates progression of the reaction. 2. **Reaction 2:** - **Reactant:** A cyclic anhydride, depicted as a six-membered ring with two carbonyl groups at opposite positions. - **Reagent:** Amino-propene (specifically an allylamine), with a (1 eq.) notation, indicating the use of one equivalent. - **Arrow:** Indicates progression of the reaction. These reactions often involve protection and deprotection steps or attaching functional groups for synthesis in organic chemistry.
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