Vinyl bromide undergoes :

Neopentyl bromide undergoes nucleophilic substitution reactions very slowly. Why?

Neopentyl bromide undergoes dehydrohalogenation to give alkene even though it has no beta -hydrogen. This is due to :

Neopentyl bromide undergoes dehydro halogenation to give alkene even though it has no beta- hydrogen. This is due to :

Neopentyl bromide undergoes dehydro halogenation to give alkene even though it has no beta- hydrogen. This is due to :