is either of the reactions biomolecular? ### Chemical Reactions**Reaction 3:**The structure on the left side represents a brominated aromatic compound esterified with acetic acid derivatives. The reaction proceeds to produce a cyclic anhydride (four-membered ring) and a brominated phenolate ion. - **Reactant:**\ ![Left Structure](#) \ Includes an aromatic ring with a bromine (Br) atom attached, connected through an ester linkage to two acetic acid groups.- **Products:**\ ![Right Structures](#) \ Formed are a cyclic structure with four carbon atoms double-bonded to two oxygen atoms (cyclic anhydride) and a brominated phenolate ion.- **Reaction Rate:**\ \(2 \times 10^5\)**Reaction 4:**The structure on the left side is a bicyclic compound esterified with acetic acid derivatives. The reaction results in another bicyclic structure with an anhydride and a brominated phenolate ion.- **Reactant:**\ ![Left Structure](#) \ Shows a bridged bicyclic compound with an attached brominated aromatic group and two esterified acetic acids.- **Products:**\ ![Right Structures](#) \ Produced are a bicyclic compound with an anhydride functional group and a brominated phenolate ion.- **Reaction Rate:**\ \(5 \times 10^7\)**Note:** Each reaction equation shows the transformation of specific chemical structures, indicating the products formed along with their associated reaction rates, denoted in scientific notation.

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Answered: H2C-C-0- H2 2x 105 3. H,c-c-00 -Br H,C…

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Chemistry

H2C-C-0- H2 2x 105 3. H,c-c-00 -Br H,C Br 5x107 -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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