The reaction involves 1-bromobutane (an alkyl halide) with potassium hydroxide (KOH) in ethanol. This is a typical example of an elimination reaction (E2 mechanism), where the hydroxide ion (OHâ») removes a proton from the carbon adjacent to the carbon that is bonded to the leaving group (Brâ»), leading to the formation of a double bond.
Step 1: Identify the type of reaction
Since the reaction is occurring in ethanol, which is a polar protic solvent, the elimination occurs via the E2 mechanism.
Step 2: Identify the product
- The E2 mechanism will lead to the formation of an alkene.
- The hydrogen is removed from the carbon next to the carbon bearing the bromine (the β-carbon), leading to the formation of But-2-ene.
Answer: The major product of the reaction is But-2-ene, and thus the correct answer is option (2).