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 :

Neopentyl bormide, undergoes dehydrohalogenation to give alkenes even though it has no beta-H . This is due to

Neopentyl bromide undergoes nucleophilic substitution reactions very slowly. Why?

Vicinal dihalides undergo double dehydrohalogenation to give terminal alkyne. How many moles of NaNH_2 are used in the overall reaction?

Vicinal dihalides undergo double dehydrohalogenation to give terminal alkyne. How many moles of NaNH_2 are used in the overall reaction?