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- W2061761698 abstract "The reactions of sulphuryl chloride with anisole and some methyl-substituted anisoles have been studied kinetically in chlorobenzene as solvent. The reactions have the kinetic form –d[SO2Cl2]/dt=k2[ArH][SO2Cl2], and give almost exclusively the products of nuclear chlorination. The rate is powerfully facilitated by the electron-releasing effect of methyl groups in the nucleus. The results are interpreted as indicating that the reactions are heterolytic, and probably involve electrophilic attack by molecular sulphuryl chloride." @default.
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- W2061761698 date "1967-01-01" @default.
- W2061761698 modified "2023-10-18" @default.
- W2061761698 title "Sulphuryl chloride as an electrophile for aromatic substitution" @default.
- W2061761698 doi "https://doi.org/10.1039/j29670001044" @default.
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