FREE RADICAL SUBSTITUTION. PART 34. THE CHLORINATION OF 1- AND 2-NITROBUTANES IN THE GAS AND LIQUID PHASES
1- and 2-nitrobutanes have been chlorinated in the gas phase and in solution.The intermediate nitrobutyl radicals with the nitro-group in a β-position are unstable and in the gas phase lose NO2 to yield the corresponding butene.The relative rates of attack at the various sites have been determined.The nitro-group proves to be the most deactivating non-ionic substituent studied so far.
Saeed-y-Atto,Potter, Alan,Singh, Hari,Tedder, John M.
p. 139 - 142
(2007/10/02)
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