**Organic Reaction Question:**Add the necessary reaction conditions above or below the arrow in this organic reaction.**Instructions:**- If a major product is missing from the right-hand side, draw it in.**Diagram Explanation:**- The left side of the reaction shows an epoxide, characterized by a three-membered ring with an oxygen atom, often represented by a triangle. - The right side of the reaction displays a molecule with an alcohol group (OH) on the second carbon and a bromine atom (Br) on the third carbon, suggesting a potential ring-opening reaction of the epoxide.**Key Points to Consider:**- Determine the reaction conditions required for the epoxide to convert into the bromo alcohol shown.- Consider if the reaction may need an acid or base to facilitate the ring-opening of the epoxide.**Next Steps:**- Insert the appropriate conditions and/or other products, if needed, to complete the reaction.

Given reaction is epoxide ring opening under acidic condition Oxygen of epoxide takes proton and get protonated. Then nucleophilic attacks on carbon of epoxide to open ring.

Answered: TPA Add the necessary reaction…

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TPA Add the necessary reaction conditions above or below the arrow in this organic reaction. Also, if a major product is missing from the right-hand side, draw it in. Ст с + T X HO 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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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

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