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Haloalkane
Alkyl nitrite
Nitroalkane
Hydrocarbon
The transition state is stable
The complete mechanism takes place in a single step
The rate of the reaction depends on the concentration of both reactants
There is an inversion of configuration
aliphatic halogen compound
side-chain substituted aryl halide
alkyl halide
aromatic halogen compound
Allyl bromide
Vinyl bromide
Tert-Butyl bromide
Propylidene bromide
1,2-Dichloroethane
Ethylene dichloride
Ethylidene chloride
Vic-dichloride
red phosphorous
concentrated H2SO4
anhydrous ZnCl2
pyridine
Phosphorus acid
Phosphoryl chloride
Phosphorus trichloride
Phosphoric acid
Chloromethane
Tetrachloromethane
Trichloromethane
Dichloromethane
para>ortho>meta
meta>ortho>para
ortho>meta>para
para>meta>ortho
It results in the formation of a vicinal dihalide
It results in the discharge of a reddish-brown colour
It results in the formation of a colourless compound
It results in the breaking of the C-C double bond