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.

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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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Identify the reagents a–c in the following scheme:

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

Draw and name all of the monochlorination products that you might obtain from the radical chlorination of the compounds below. Which of the products is chiral? Are any of the products optically active?
(a) 2-methylbutane
(b) Methylcyclopropane
(c) 2,2-dimethylpentane
Tertiary alkyl halides,, undergo spontaneous dissociation to yield a carbocation,, plus halide ion. Which do you think reacts faster,? Explain.
What products would you expect from reaction of the following alkenes with NBS? If more than one product is formed, show the structures of all.

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