An aromatic compound ‘A’ with molecular formula C8H8O gives positive 2,4-DNP test. It gives yellow precipitate of compound ‘B’ on treatment with sodium hypoiodite. Compound ‘A’ does not react with Tollen’s or Fehling’s reagent; on drastic oxidation with KMnO4 it forms a carboxylic acid ‘C’. Elucidate the structures of A, B, and C. Also give their IUPAC names.
The reaction between A2 (g) and B2 (g) was carried out in a sealed isothermal container. The rate law for the reaction was found to be:
Rate = \( k[\text{A}_2][\text{B}_2] \)
If 1 mole of A2 (g) was added to the reaction chamber and the temperature was kept constant, then predict the change in rate of the reaction and the rate constant.
Name the type of isomerism exhibited and draw isomers:
(I) [Co(NH3)6][Cr(CN)6]
(II) [Co(en)3]3+
(III) [Co(NH3)3(NO2)3]