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- W2949217422 abstract "Various alkyl-substituted p-dimethoxybenzenes (ArH) react readily with nitric acid and sulfuric to form nitro-products (ArNO 2 ). When the nitric acid is used in excess, the nitro-product react via either nitration to dinitro-compound (Ar(NO 2 ) 2 ) or via oxidative demethylation to nitro- p-quinone (Q). As such, the competition between the nitration, polynitration and oxidative dealkylation is effectively modulated by the added nitric acid and the alkyl-substituted p-dimethoxybenzenes." @default.
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- W2949217422 date "2000-03-01" @default.
- W2949217422 modified "2023-09-25" @default.
- W2949217422 title "The dichotomy between nitration of substituted 1,4-dimethoxybenzenes and formation of corresponding 1,4-benzoquinones by using nitric and sulfuric acid" @default.
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- W2949217422 doi "https://doi.org/10.3184/030823400103166788" @default.
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