**Problem 35 of 44**Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s).Be sure to account for all bond-breaking and bond-making steps.**Diagram:**1. **Reactants:** - Organic molecule with a chlorinated carbon chain and secondary amine (NH2-). - Sodium cation (Na⁺). - Cyclopentyl group.2. **Reagents:** - Sodium amide (NaNH₂). - Tetrahydrofuran (THF).**Conditions:** - Heat**Products:** - Chlorinated cyclopentane derivative. - Sodium cation (Na⁺). - Amino group (NH2) attached to the organic chain.In the reaction, the curved arrows should be used to indicate the movement of electrons leading to bond formation or cleavage. Ensure to include steps for both bond-breaking and bond-making processes in your arrow-pushing mechanism.

This is an E2 reaction, final product is produce is alkene

urved arrows are used to illustrate the low of electrons. Using the provided rting and product structures, draw the rved electron-pushing arrows for the owing reaction or mechanistic step(s). sure to account for all bond-breaking and bond-making steps. HH O HH CI heat H Select to Add Arrows O Ĵ NaNH2, THF H Na O CI O Na Ⓒ

urved arrows are used to illustrate the low of electrons. Using the provided rting and product structures, draw the rved electron-pushing arrows for the owing reaction or mechanistic step(s). sure to account for all bond-breaking and bond-making steps. HH O HH CI heat H Select to Add Arrows O Ĵ NaNH2, THF H Na O CI O Na Ⓒ

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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