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[Review Topics] [References] The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond W You do not have to consider stereochemistry. 1 You do not have to explicitly draw H atoms. ■ Separate resonance structures using the 2 symbol from the drop-down menu. . Include all valence radical electrons in your answer. Sn [] K
[Review Topics] [References] The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond. U You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • Separate resonance structures using the J symbol from the drop-down menu. • Include all valence radical electrons in your answer. Sn (1 *****
[Review Topical [References] The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. s Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond. ed . You do not have to consider stereochemistry. ■ You do not have to explicitly draw H atoms. ■ Separate resonance structures using the symbol from the drop-down menu. . Include all valence radical electrons in your answer. 981 *****