Concept:An alkene reacts with concentrated tetraoxosulphate (VI) acid by electrophilic addition, forming an alkyl hydrogen sulphate which is later hydrolysed to an alkanol.
Explanation:When an alkene is passed into concentrated
H2SO4, the acid adds across the double bond.
This addition produces an alkyl hydrogen tetraoxosulphate (VI), e.g.
C2H5HSO4 from ethene.
On boiling this product with water, hydrolysis occurs to give the corresponding alkanol and regenerate the acid.
Representative equations:
C2H4+H2SO4→C2H5HSO4C2H5HSO4+H2O→C2H5OH+H2SO4Bromine in tetrachloroethane produces a dibromoalkane, not an alkanol.
Aqueous
KMnO4 can give a diol, while sodium hydroxide solution does not form an alkanol from an alkene under these conditions.
Answer:A. concentrated tetraoxosulphate (VI) acid