The bond dissociation energy needed to form the benzyl radical from toluene is $.....$ than the formation of the methyl radical from methane.

  • A
    Less
  • B
    Much
  • C
    Equal
  • D
    None of the above

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Similar Questions

What is the decreasing order of stability (most stable $\to$ least stable) of the following carbocations?

Which is the decreasing order of stability?
$(i)$ $CH_3-CH^{+}-CH_3$
$(ii)$ $CH_3-CH^{+}-OCH_3$
$(iii)$ $CH_3-CH^{+}-COCH_3$

Which of the following is the least stable carbocation?

Which of the following carbocations is most stable?

Explain why $((CH_3)_3C)^+$ is more stable than $(CH_3CH_2)^+$ and $(CH_3)^+$ is the least stable carbocation.

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