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1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms...


1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms when appli
1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. 2. Rank the following free radical intermediates in order of increasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. CH2 bro ledo IV b III 10 112TV ] 21 3. 2,3-Dimethylbutane reacts with bromine in the presence of light to give a monobrominated product. Predict the structure of the monobrominated product and propose a mechanism for its formation.
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(+) Secondary carbocation I t (+) allylie-Casbocation (+) rTr Primary-carbocation | Телаяу-саяЫocation IV Rank of the cVV becondasy. Allylie Radical more stable Form Но Benzylic- Radical TIL) Tertiaay. Radical 112 • Primary Radical - In Rank(3) Hac - CH – CH – CH3 Bra Hz CH — — CH3 ен, енд К) CH3 CH₃ 2,3-dimethylobutane a-bromo-2, 3-di- methyl- butane 23. dimethylMechanismo от, му , В. + Вр. of Br H3 C CH - CH₂ не — сH — — ең, ендон, ін, ең, teatasy-Radical of H BY Br. Br H, C— СА — — с

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