Terminal alkynes are more acidic than other hydrocarbons due to the stability of the acetylide anion.
The sp hybrid orbital of the acetylide anion has more s character than sp2 or sp3 orbitals and hence is closer to the nucleus. As a result the negative charge is stabilised the most in the alkynes.
Strong bases are required to deprotonate alkynes such as soda amide and potassium amide.
R-C≡C-H + NH2- → R-C≡C- + NH3