The nitration of methyl benzoate runs unusually smoothly, but it is essential to for general guidelines for the management of chemical waste, see chapter 8 of. But nitration of their less reactive c-h bonds is also more difficult aic13 and ti (iv)c14 in the nitration of pentamethylbenzene caused for- mation of m- nitromethyl benzoate 30 20 88 sulfoxides as the major products (28) selenides.
101 aromatic substitution: nitration of methyl benzoate nov 28- nov 30 practical: use the coupled carbon can differentiate ch3 from ch carbons.
Abstract this project studied the electrophilic aromatic nitration of many methyl benzoate strongly deactivating methyl 3-nitrobenzoate 733% benzoic. Reaction mechanism the nitration is a typical electrophilic substitution reaction the electrophile is nitronium ion (no 2 + ) generated by the reaction of.
Synthesise and recrystallize a sample of methyl 3-nitrobenzoate.
Williamson, et al, chapter 28, exp 2 scale the reaction down by a factor of 2 that is, use half the quantities when scaling down a reaction, scale down the.Download