Answer: B, C, D
A larger s-character stabilises the carbanion, giving the acidity order ethyne > ethene > ethane. The conjugate acid of acetylide (ethyne, pKa≈25) is weaker than water (15.7), so acetylide is the stronger base and is protonated by water, regenerating ethyne. For the same reason aqueous NaOH cannot convert ethyne to its anion to any significant extent.