结果表明，尽管这些二甲基萘的电离能基本相同，但因取代基位置不同使分子中电荷分布不同，从而影响了激基复合物的形成能力。
Although the ionization potentials of dimethyl naphthalenes used was almost the same yet the charge distribution was different due to the different positions of two methyl groups on naphthalene. Th…
芳基上取代基的位置和性质以及使用的溶剂都能够影响非对映体2r, 4r和2s, 4r在溶液中的相对含量。
The relative contents of diastereomers, 2r 4r and 2s 4r, in solution are influenced by both the solvents used and the characteristics and locations of substituents on 2-aryl.
亲电基取代位置和实验值完全一致。
The substituting position of electrophilic group accord with experimental value.
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