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1.78 (a) Add curved arrows to show how the starting material A is converted to the product B. (b) Draw all reasonable resonance structures for B. (c) Draw the resonance hybrid for B. B

1.78 (a) Add curved arrows to show how the starting material A is converted to the product B. (b) Draw all reasonable resonance structures for B. (c) Draw the resonance hybrid for B. B

Introductory Chemistry: An Active Learning Approach
Introductory Chemistry: An Active Learning Approach
6th Edition
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Mark S. Cracolice, Ed Peters
Chapter13: Structure And Shape
Section: Chapter Questions
Problem 57E
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**Exercise 1.78** **Objective:** (a) Add curved arrows to show how the starting material A is converted to the product B. (b) Draw all reasonable resonance structures for B. (c) Draw the resonance hybrid for B. **Description:** The image presents a chemical reaction where starting material A is transformed into product B. - **Structure A**: It is a long-chain hydrocarbon with a chlorine (Cl) atom at the end. - **Structure B**: Product B consists of a cyclohexyl ring with an adjacent chain, showcasing a carbocation (positively charged carbon) and the chloride ion (Cl-) as a separate entity. - **Task**: - **(a)** Add curved arrows to depict electron movement that leads to the formation of B from A. - **(b)** Envision and illustrate all resonance forms arising from the delocalization of the positive charge in B. - **(c)** Portray the resonance hybrid for B, indicating partial charge distribution and electron delocalization. This exercise aims to enhance understanding of mechanistic pathways, resonance theory, and the conceptualization of structures in organic chemistry.
Transcribed Image Text:**Exercise 1.78** **Objective:** (a) Add curved arrows to show how the starting material A is converted to the product B. (b) Draw all reasonable resonance structures for B. (c) Draw the resonance hybrid for B. **Description:** The image presents a chemical reaction where starting material A is transformed into product B. - **Structure A**: It is a long-chain hydrocarbon with a chlorine (Cl) atom at the end. - **Structure B**: Product B consists of a cyclohexyl ring with an adjacent chain, showcasing a carbocation (positively charged carbon) and the chloride ion (Cl-) as a separate entity. - **Task**: - **(a)** Add curved arrows to depict electron movement that leads to the formation of B from A. - **(b)** Envision and illustrate all resonance forms arising from the delocalization of the positive charge in B. - **(c)** Portray the resonance hybrid for B, indicating partial charge distribution and electron delocalization. This exercise aims to enhance understanding of mechanistic pathways, resonance theory, and the conceptualization of structures in organic chemistry.
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