Why is benzene unusually stable and why does it prefer substitution to addition?
Hydrocarbons
Original Khojo Papers practice question — not from a past board paper.
Nitration with a mixture of concentrated nitric and sulphuric acids. Halogenation with chlorine or bromine in the presence of anhydrous aluminium chloride or iron(III) bromide. Friedel-Crafts alkylation or acylation with an alkyl or acyl halide and anhydrous aluminium chloride. Sulphonation with fuming sulphuric acid is a fourth.
No citable source has been recorded for this record. Treat it as practice material, not as fact.
In each case an electrophile attacks the delocalised pi system and a proton is lost, so the ring survives.
From the same topic and chapter, at a similar level.
Why is benzene unusually stable and why does it prefer substitution to addition?
Hydrocarbons
Why do alkanes undergo substitution while alkenes undergo addition?
Hydrocarbons
Describe the mechanism of the free radical substitution of methane by chlorine in sunlight.
Hydrocarbons
State Markownikoff's rule and apply it to the addition of hydrogen bromide to propene.
Hydrocarbons
What is the Wurtz reaction, and state its main limitation.
Hydrocarbons
State Hund's rule and the Aufbau principle.
Structure of Atom