Nameofnitrocompound Biotransformedproduct FTIR(cm-1) 1HNMR(300MHz,CDCl3)
3-Nitrobenzoinc acid 3-Aminobenzoic acid 2970(broad,N-Hstre) δ7.5(d,J=7.9Hz,1H)
1685(weak,C=Ostre) δ7.4(s,1H)
1633(med,C=Caromatic) δ7.2(m,1H)
1572(med,C=Caromatic) δ6.9(d,J=7.8Hz,1H)
1450(med,C=Caromatic) δ3.5(bs,2H)
766(sharp,1,3-disubstituted)  
4-Nitro toluene p-Toluidine 3417(medium,N-Hsymt) δ7.0(d,J=8.0Hz,2H)
3340(sharp,N-Hasymmetric) δ6.6(d,J=8.0Hz,2H)
3022(med,C-Haromatic) δ3.5(s,2H)
2918(weak,C-Haliphatic) δ2.2(s,3H)
1620(med,C=Caromatic)  
1518(medium,C=Caromatic)  
813(sharp,1,4-disubstituted)  
3-Nitro toluene 3-Amino toluene 3433(med,N-Hsymmetric) δ7.0(t,J=8.0Hz,1H)
3354(sharp,N-Hasymmetric) δ6.5(d,J=1.5Hz,1H)
3034(med,C-Haromatic) δ6.4(m,2H)
2918(weak,C-Haliphatic) δ3.5(bs,2H)
1622(med,C=Caromatic) δ2.2(s,3H)
1591(med,C=Caromatic)  
1492(med,C=Caromatic)  
1417(med,C=Caromatic)  
775(sharp,1,3-disubstituted)  
1-Chloro 2-nitrobenzene 2-Chlorobenzenamine 3471(med,N-Hsymmetric) δ7.2(d,J=8.0Hz,1H)
3391(sharp,N-Hasymmetric) δ7.1(d,J=7.8Hz,1H)
3070(weak,C-Haromatic) δ6.8(m,2H)
1614(med,C=Caromatic) δ4.0(s,2H)
1485(med,C=Caromatic)  
1450(med,C=Caromatic)  
Table 3: IR and NMR analysis of bio transformed products.