The reaction between 1-bromobutane (an alkyl halide) and potassium hydroxide (KOH) in ethanol is a characteristic E2 elimination reaction. In this mechanism, the hydroxide ion (OHâ ») abstracts a proton from the carbon adjacent to the carbon bonded to the leaving group (Brâ »), resulting in the formation of a double bond.
Step 1: Determine the reaction type
Ethanol, a polar protic solvent, favors an E2 elimination mechanism.
Step 2: Identify the product
- An alkene is produced via the E2 mechanism.
- Hydrogen is removed from the carbon adjacent to the carbon bearing bromine (the β-carbon), forming But-2-ene.
Answer: The principal product of this reaction is But-2-ene. Therefore, option (2) is the correct choice.