Does the presence of two chiral carbon atoms always make the molecule optically active? Explain giving an example?

Which of the following alkenes can generate optically active compounds upon hydrogenation?

The Fischer projection of $\mathrm{D}$-erythrose is shown below.

$\mathrm{D}$-Erythrose and its isomers are listed as $\mathrm{P},\mathrm{Q},\mathrm{R},$ and $\mathrm{S}$ in Column I. Choose the correct relationship of $\mathrm{P},\mathrm{Q},\mathrm{R},$ and $\mathrm{S}$ with $\mathrm{D}$-erythrose from Column II.

	Column - I		Column -II
P.		1.	Diastereomer
Q.		2.	Identical
R.		3.	Enantiomer
S.