**Educational Content on Reaction Mechanisms**In this section, we explore the mechanisms for a series of chemical reactions. Each reaction should include the use of curved arrows and a breakdown into elementary steps emphasizing the main reaction path. If stereoisomers are produced, indicate their formation by outlining whether the result is a racemic mixture, a mixture of diastereomers, etc. As with any reactions, take caution in the representation and assignment of charges.**Reaction A**- **Reagent:** H-Br- **Conditions:** Dark- **Substrate:** An alkene with a branched alkyl group.**Reaction B**- **Sequential Steps:** 1. **Reagents:** Br2, H2O 2. **Reagent:** NaH- **Substrate:** An alkene with a simple alkyl group.**Reaction C**- **Reagent:** NaOEt (Sodium ethoxide)- **Conditions:** EtOH, heat- **Substrate:** A cyclic bromo compound with aromatic (Ph) and methoxy (OMe) substituents.**Reaction D**- **Reagent:** NBS (N-Bromosuccinimide)- **Conditions:** Heat- **Substrate:** An alkene with a phenyl group attached.For each of these reactions, consider the potential pathways and intermediate species involved. Apply the appropriate use of stereochemistry notation and ensure careful accounting for electron movement via appropriate arrows.

HBr : It is a strong acid, gives addition products with alkenes. The reaction proceeds via formation…

Answered: A. B. C. OMe Br Ph H-Br dark 1) Br-Br,…

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A. B. C. OMe Br Ph H-Br dark 1) Br-Br, H₂O 2) NaH NaOEt EtOH, heat

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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