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Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the products of the following reaction. Include all lone pairs and charges as appropriate.

Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the products of the following reaction. Include all lone pairs and charges as appropriate.

Chemistry
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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**Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the products of the following reaction. Include all lone pairs and charges as appropriate.** **Diagram Description:** The diagram shows a benzene ring (a hexagonal ring with alternating double bonds) with three curved arrows indicating the movement of electrons. Two arrows originate from the double bonds in the benzene ring, directing towards adjacent carbon-carbon bonds, suggesting the movement of pi electrons. The third arrow points from a lone pair represented by dots next to a negatively charged atom outside the benzene ring, indicating electron donation or movement towards the ring. The illustration is a depiction of a reaction mechanism, involving resonance or electron delocalization, common in aromatic systems like benzene. It highlights the importance of drawing the resulting structure after electron movement, including all lone pairs and charges.
Transcribed Image Text:**Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the products of the following reaction. Include all lone pairs and charges as appropriate.** **Diagram Description:** The diagram shows a benzene ring (a hexagonal ring with alternating double bonds) with three curved arrows indicating the movement of electrons. Two arrows originate from the double bonds in the benzene ring, directing towards adjacent carbon-carbon bonds, suggesting the movement of pi electrons. The third arrow points from a lone pair represented by dots next to a negatively charged atom outside the benzene ring, indicating electron donation or movement towards the ring. The illustration is a depiction of a reaction mechanism, involving resonance or electron delocalization, common in aromatic systems like benzene. It highlights the importance of drawing the resulting structure after electron movement, including all lone pairs and charges.
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Given : structure of reactants. 

Tip : foll the movement of arrow

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