Electrophilic aromatic substitution. Part 31. The kinetics and products of nitration of naphthalene, biphenyl, and some reactive monocyclic aromatic substrates in aqueous phosphoric acid containing nitric acid or propyl nitrate

Author(s):  
Roy B. Moodie ◽  
Kenneth Schofield ◽  
Alan R. Wait
1986 ◽  
Vol 51 (9) ◽  
pp. 2013-2018
Author(s):  
Ján Hrabovský ◽  
Jaroslav Kováč ◽  
František Považanec

Mechanism has been studied of electrophilic aromatic substitution with (Z)- and (E)-5-nitro-2-furylvinyl bromide in the presence of aluminium(III) chloride. From chemical findings and 1H NMR study it follows that the mechanism can be interpreted as an electrophilic addition-elimination pathway (AdE-E) from the point of view of the vinyl substitution.


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