Treatment of 2,4,6-tri-tert-butylphenol with bromine in cold acetic acid gives the compound c18h29bro in quantitative yield. the infrared spectrum of this compound contains absorptions at 1630 and 1655 cm^-1. its 1h nmr spectrum shows only three peaks (all singlets), at δ 1.2, 1.3, and 6.9, in the ratio 9: 18: 2. what is a reasonable structure for the compound?
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Treatment of 2,4,6-tri-tert-butylphenol with bromine in cold acetic acid gives the compound c18h29br...
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