Explain why triphenylmethane is so susceptible to autooxidation. ✓ Homolytic cleavage Hydrogen abstraction Addition to a pi bond Elimination Halogen abstraction leads to is stabilized through the production of more

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Explain why triphenylmethane is so susceptible to autooxidation.
an anion which is capable of intramolecular hydrogen bonding
dissociation of a benzyl radical
✓a radical intermediate which is stabilized through the production of more product by LeChatelier's Principle
a radical with many resonance structures
Transcribed Image Text:Explain why triphenylmethane is so susceptible to autooxidation. an anion which is capable of intramolecular hydrogen bonding dissociation of a benzyl radical ✓a radical intermediate which is stabilized through the production of more product by LeChatelier's Principle a radical with many resonance structures
Explain why triphenylmethane is so susceptible to autooxidation.
✓ Homolytic cleavage
Hydrogen abstraction.
Addition to a pi bond
Elimination
Halogen abstraction
leads to
is stabilized through the production of more
Transcribed Image Text:Explain why triphenylmethane is so susceptible to autooxidation. ✓ Homolytic cleavage Hydrogen abstraction. Addition to a pi bond Elimination Halogen abstraction leads to is stabilized through the production of more
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