Which one of the following is the most stable alkene?

More no. of$\alpha$ -hydrogens due to hyperconjugation.

Hyperconjugation effect decides the stability of free radicals, carbocations and alkenes, Hyperconjugation effect depends on the number of alpha hydrogen present on the alpha carbon with reference to the benzene ring or the radical/C=C/positive or the carbon chain. More the hydrogens more the hyperconjugation forms. It involves the overlap of  sigma with p-orbital overlap.