b Carrying out dehydrohalogenation with a bulky base such as potassium tert-butoxide ( \(t\) -\(BuOK\) ) in \(1,2\) -diphenyl1-bromoethane \((t-\mathrm{BuOH})\) favors the formation of the alkene via \(E_2\) mechanism. The reaction involved is
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