A strong base removes acidic protons followed by loss of leaving group i.e. first a group or atom without its electron pair is lost, usually proton and then a group with its electron pair is lost.
These reactions are favored by
Presence of electron withdrawing group on α carbon atom (i.e. acidity of α hydrogen is increased). It is supported by the fact that reaction of alkyl bromides or iodides with base gave very less α elimination product than that of corresponding alkyl chlorides.
Use of very strong base favors α elimination. PhNa , a very strong base gave α elimination product in following reaction up to 94% whereas NaNH 2 or NaOMe did not give much yields.
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