Elimination reactions (especially `beta`-elimination) are as common as the nucleophilic substitution reaction in case of alkyl halides. Specify the reagents used in both cases.

Explanation

Elimination reactions are as common as the nucleophilic substitution reaction in case of alkyl halides as two reactions occur simultaneously. Generally, at lower temperature and by using weaker base, nucleophilic substitution reactions occur while at higher temperature and by using a stronger base, elimination reactions (especially `beta` -elimination) take place.
e.g. If ethyl bromide is treated with aq. KOH at low temperature, it gives ethanol while if it is treated with alc. KOH at high temperature then it gives ethene.
`underset(("Nucleophilic substitution reaction"))(CH_(3)CH_(2)Brunderset(373K)overset(Aq.KOH)rarrunderset("Ethanol")(CH_(3)CH_(2)OH))`
`CH_(3)CH_(2)Brunderset(473-523K)overset(Alc.KOH)rarrunderset("Ethene")(CH_(2)=CH_(2))` (Elimination reaction)