Chapter 10: Q10-36E (page 308)
Draw resonance structures for the benzyl radical, the intermediate produced in the NBS bromination reaction of toluene (Problem 10-35).
Short Answer
Here four resonating structures are possible.

Chapter 10: Q10-36E (page 308)
Draw resonance structures for the benzyl radical, the intermediate produced in the NBS bromination reaction of toluene (Problem 10-35).
Here four resonating structures are possible.

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Question: Addition of HBr to a double bond with an ethersubstituentoccurs regiospecifically to give a product in which theandare bonded to the same carbon. Draw the two possible carbocation intermediates in this electrophilic addition reaction, and explain usingresonance why the observed product is formed.

Draw three resonance forms for the cyclohexadienyl radical.

Cyclohexadienyl radical
Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br∙ and
(c)

Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br∙ and Br2.
(b)

Give IUPAC names for the following alkyl halide (e):

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