The C-H bonds shown in red exhibit very similar BDEs, because homolytic cleavage of either bond results in a resonance-stabilized radical. Nevertheless, one of these C-H bonds is weaker than the other. بہت Identify the weaker bond, and explain your choice: C-H, is weaker, because there is more steric hindrance C-H, is weaker, because there is less steric hindrance OC-H, is weaker, because resonance involves a tertiary radical C-H, is weaker, because resonance involves a tertiary radical

The C-H bonds shown in red exhibit very similar BDEs, because homolytic cleavage of either bond results in a resonance-stabilized radical. Nevertheless, one of these C-H bonds is weaker than the other. بہت Identify the weaker bond, and explain your choice: C-H, is weaker, because there is more steric hindrance C-H, is weaker, because there is less steric hindrance OC-H, is weaker, because resonance involves a tertiary radical C-H, is weaker, because resonance involves a tertiary radical

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 4E

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