Answer:
The correct answer is B the tertiary halides reacts faster than primary halides.
Explanation:
During SN2 reaction the nucleophile attack the alkyl halide from the opposite side resulting in the formation of transition state in which a bond is not completely broken or a new bond is not completely formed.
After a certain period of time the nucleophile attach with the substrate by substituting the existing nuclophile.
An increase in the bulkiness in the alkyl halide the SN2 reaction rate of that alkyl halide decreases.This phenomenon is called steric hindrance.
So from that point of view the that statement tertiary halides reacts faster that secondary halide is not correct.
Reactant: <span>Cd(NO^3)^2+(aq)+H^2S(g)
</span>Product: <span>Cds(s)+2HNO^3(aq)</span>
It is affected because it changes the charge of the ions their size and their ability to create hydrogen bonds with the solvent
