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Q: CI CH3 CHCHCH3 CH, CHCH CH, • cí CH3 CH3
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- Considering the indicated carbon–halogen bonds, which bond is predicted to have the higher bond dissociation energy? Which bond is stronger?Rank the following radicals in order of decreasing stability (most stable to least stable). II IV A IV >T> II > II B III >1> I > IV Al IV > II > I E Il > III > I > VArrange the following free radicals in order of increasing stability
- (Reviow Toples) [References Use the References to access important values if needed for thi Draw a structural formula for the organic anion (i.e., do not include K or Nat) formed from the following reaction. Don't forget the charge on the ion. + KOH нсон • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include all nonzero formal charges. P. opy aste [F CH4 ChemDoodle"Which resonance structure in each of the following pairs is more stable? Why?Which is the mos) Stable radical. B) oi N c) D) N €)
- Classify the radicals into the appropriate categories. Primary, Secondary, Tertiary, AllylicWhat is the formal charge on the O atom in each of the following species that contains a multiple bond to O?Write EACH MAJOR CARBON-CONTAINING product(s) and box your final answer(s) or write them in the answer line provided. If a new product is not possible, write “No Rxn”. When the product has an oxygen with a negative formal charge, assume that acid is added at the end to resolve the negative formal charge.... please use the format provided