Are these groups activating or deactivating, ortho/para or meta directors? Table 2 EAS data and results....
Electropholic Aromatic Substitution
Table 1: Pre-Lab table Compound Structure of the compound Group present on the benzene ring Toluene Do web browser bueno besed oborio Aniline namiot babilom in Phenyl Acetate Acetanilide Anisole Methyl Benzoate Acetophenone Benzaldehyde Chlorobenzene Table 1: Pre-Lab table Compound Structure of the compound Group present on the benzene ring Toluene Aniline Phenyl Acetate Acetanilide Anisole Methyl Benzoate Acetophenone Benzaldehyde Chlorobenzene
Label the following as activating (A) or deactivating (D), and then also as ortho/para directors (OP) or meta directors (M). Write the answer below each group. N "Here with other ty A/D? = = = = OP/M? = f) Using resonance structures, explain why a nitro group is "meta-directing" (i.e. does the nitro group actually affect the meta positions?) g) As mentioned in class, the halogens are a bit anomalous as substituents on the aromatic ring: they are deactivating groups,...
5. All electron-donating groups are activating groups and all are ortho-para directors with the exception of substituents, all electron-withdrawing groups are deactivating groups and all are meta directors. A. hydroxyl B. amino C. halogens D. alkoxyl 6. Hydrogen abstraction from the methyl group of methylbenzene (toluene) produces a radical called the radical. A. allylic B. free C. halogen D. benzyllic 7. The stability of benzyllic radicals can be explained by theory. A. resonance B. bond order C. inductive D. molecular...