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.
An alkane is saturated: all its bonds are strong sigma bonds and there is no site of electron density to attract a reagent, so it can only have one atom replaced by another. An alkene has a pi bond whose electrons are loosely held and exposed, which attracts electrophiles and lets a reagent add across the double bond to give a more stable saturated product.
No citable source has been recorded for this record. Treat it as practice material, not as fact.
This is why bromine water distinguishes the two.
From the same topic and chapter, at a similar level.
Why is benzene unusually stable and why does it prefer substitution to addition?
Hydrocarbons
Name three electrophilic substitution reactions of benzene with the reagent used in each.
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