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.
In the Wurtz reaction an alkyl halide is heated with sodium in dry ether and two alkyl groups join to give a higher alkane. Its limitation is that it works well only for a symmetrical alkane: two different halides give a mixture of three products that is hard to separate, and methane cannot be prepared by it at all.
No citable source has been recorded for this record. Treat it as practice material, not as fact.
The reaction always gives an alkane with an even number of carbon atoms when a single halide is used.
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
Name three electrophilic substitution reactions of benzene with the reagent used in each.
Hydrocarbons
State Hund's rule and the Aufbau principle.
Structure of Atom