The image shows a chemical reaction transformation starting from 1-bromopropane to a more complex organic molecule. On the left side of the diagram, 1-bromopropane is illustrated by a straight chain of three carbon atoms, with a bromine (Br) atom attached to the terminal carbon. An arrow points from 1-bromopropane to the product on the right.The product on the right of the arrow is a more complex organic molecule featuring two ester functional groups (RCOOR'). The structure consists of a chain of seven carbon atoms. Starting from the left, there is an ester linkage (–C(=O)O–) with a carbonyl group adjacent to it. The center carbon atom in the chain exhibits stereochemistry, indicated by the wedge-and-dash notation. Another ester group is present mid-structure, and the chain terminates with two additional carbon atoms bonded to a carbonyl group each.Overall, the diagram depicts a conversion of a simple alkyl halide into a more complex molecule containing multiple functionality and stereochemical features. This image presents a flowchart depicting a series of organic chemical reactions involving various functional groups. The diagram includes starting materials, intermediates, and final products, along with reagents and conditions required for each transformation.**Reaction Pathways:**1. **Path A:** - Starts with an alcohol (R–OH). - Converts to a carboxylic acid (R–COOH).2. **Path B:** - Begins with a carboxylic acid (R–COOH). - Proceeds through an acid-catalyzed hydration step involving H₃O⁺. - Results in an alcohol (R–OH).3. **Path C:** - Carboxylic acid (R–COOH) reacts with NaOH followed by CH₃CH₂I. - Forms an ester (RCOOCH₂CH₃).4. **Path D:** - Carboxylic acid (R–COOH) is converted to an acid chloride (R–COCl).5. **Path E:** - Acid chloride (R–COCl) undergoes reaction to form an amide (R–CONH₂).6. **Path F:** - Amide (R–CONH₂) undergoes further reaction. - Produces a secondary amine (R–NH–CH₃).7. **Path G:** - Involves a different transformation pathway starting from a diester compound. - No specific reagents detailed for this transformation in the image.This diagram serves as a guide for understanding the conversion between different organic compounds using specific reagents, showcasing principles of organic synthesis.

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Answered: must be made from the starting…

Science

Chemistry

must be made from the starting 1-bromopropane. Br

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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