Step 1: Under acid–catalysed aldol conditions, aldehydes first form a β-hydroxy aldehyde.
Step 2: Acidic medium favours dehydration, leading to formation of an α,β-unsaturated aldehyde (conjugated system).
Step 3: In both aldehydes (I) and (II), the more substituted alkene is favoured due to greater stability.
Step 4: Hence, the major products are the conjugated enals shown in option (b).