We can use single electron (fishhook) arrows to draw resonance structures just as we can with regular two electron arrows. When drawing resonance structures with pi bonds, the pi bond will be cleaved homolytically. Given the structure shown below, what resonance structure is invalid? benzyl radical: C: B: A: D:

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter5: Resonance
Section: Chapter Questions
Problem 35CTQ
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Which structure is correct? Please include the arrow pushing & resonance to guide me

We can use single electron (fishhook) arrows to draw resonance structures just as we can with regular two electron arrows. When drawing resonance structures with pi
bonds, the pi bond will be cleaved homolytically.
Given the structure shown below, what resonance structure is invalid?
benzyl radical:
C:
B:
A:
D:
Transcribed Image Text:We can use single electron (fishhook) arrows to draw resonance structures just as we can with regular two electron arrows. When drawing resonance structures with pi bonds, the pi bond will be cleaved homolytically. Given the structure shown below, what resonance structure is invalid? benzyl radical: C: B: A: D:
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