In radical reactions, there are sometimes non-halogenated side products formed from other termination steps. Choose the possible side product of the reaction shown below? Br2 hv A B 11 C III III IV IV D
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- Which mechanism is this reaction most likely to use? SN1 OSN2 NaSH SHWhich solvent is most often used in allylic and benzylic bromination reactions, which both proceed via radical intermediates? CH3CI CH₂Cl2 CHC13 CC14Write out the mechanism (intermediate/transition state) for this reaction; Br CH3 NaOCH₂ E₂
- There is great excess of H2O in this reaction.H202 Ho write the mechanism of each reaction)methanol + CH3OH Suppose you were told that the above reaction was a substitution reaction but you were not told the mechanism. Evaluate the following categories to determine the reaction mechanism and then draw the structure of the major organic product. Type of alkyl halide: Type of nucleophile: Solvent: Is the product racemic?