A. O – chloronitrobenzene
B. P – chloronitrobenzene
C. M – chloronitrobenzene
D. A & b
A. Cr2o3 + a2o3 + sio2
B. Raney nickel
C. Organo-nickel
D. Ni 250 – 300°c
A. Heating sod. salt of benzoic acid with soda lime
B. Distilling phenol with zn dust
C. Chlorobenzene with naoh at 360°c & 150atm.
D. Hydrolysis of benzene sulphonic acid with super heated steam
A. The rupturing of benzene ring
B. Substitution reaction
C. Addition reaction
D. No-reaction
A. Hso4-
B. So2
C. So3
D. H+
A. Benzene
B. Nitro benzene
C. Toluene
D. Chlorobenzene
A. On hydrogenation 208 kj/mole is liberated
B. C-h bond length in benzene is 1.09 a?
C. Molecular mass of benzene is 78.108
D. Resonance energy of benzene is 150.5 k cal/mole
A. Dows process
B. Friedel & craft acylation
C. Friedel & craft alkylation
D. Clemmenson reduction
A. Toluene
B. Ethyl benzene
C. N-propyl benzene
D. All
A. C6h6o9
B. C6h5o8
C. C6h5o9
D. C6h6o6