**Retrosynthesis Analysis for Educational Study****Objective:** Develop a retrosynthesis of the given target molecule shown in the diagram. The task is to identify what two compounds can be used in the last step of the synthesis to produce the desired target molecule.**Target Molecule:**- The structure features: - A benzene ring with an attached tertiary alcohol group (OH) and an amine group (NH) on adjacent carbon atoms.**Retrosynthesis Goal:**- Decompose the target molecule into two simpler starting materials that will combine to form the target in the final synthesis step.**Diagram Explanation:**- The target molecule is represented with an arrow indicating retrosynthetic analysis into two unknown components denoted by "? + ?".**Compound Options:**- The task is to select the best TWO starting materials from the list below.1. **Option 1:** - Structure: An amine (NH) group attached to a propene group (-CH3 and double bond). 2. **Option 2:** - Structure: A phenyl group attached to an acetone group (carbonyl group =O at the ketone position). 3. **Option 3:** - Structure: N-methyl amine group connected to a propene group. 4. **Option 4:** - Structure: Phenyl group attached to an oxirane (epoxide) group. 5. **Option 5:** - Structure: Phenyl group attached to a tertiary butanone group. 6. **Option 6:** - Structure: Amine group (NH) with a propyl side chain. 7. **Option 7:** - Structure: Methyl amine (CH3NH2).**Instruction:**- Identify and select the best TWO starting materials that reflect the reverse synthesis of the target molecule.**Purpose:** This exercise is designed to enhance your understanding of synthetic strategies and deepen your conceptual knowledge of organic chemistry synthesis techniques.

An arrow always depicts from a region of high electron density to low electron density ; that is…

Develop a retrosynthesis of the given target molecule, as shown below. In other words, what two compounds can be used in the last step of the synthesis to make the desired target molecule, as described in the problem statement? HO OXA From the choices given below, identify the best starting materials for the retrosynthesis above. Select TWO compounds. H CH3 CH3 + ? --U.NU

Develop a retrosynthesis of the given target molecule, as shown below. In other words, what two compounds can be used in the last step of the synthesis to make the desired target molecule, as described in the problem statement? HO OXA From the choices given below, identify the best starting materials for the retrosynthesis above. Select TWO compounds. H CH3 CH3 + ? --U.NU

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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