Step 1: Read the starting molecule.
Compound Z is an allylic alcohol, an $-OH$ sitting next to a carbon-carbon double bond. It holds one $C\!=\!C$ double bond.
Step 2: Meaning of isohypsic.
An isohypsic change is redox neutral, the overall oxidation level of carbon does not move. For an allylic alcohol this shifts the double bond and turns the $-OH$ into a carbonyl.
Step 3: Track the double bonds.
The original $C\!=\!C$ disappears, but a new $C\!=\!O$ appears in its place. One double bond out, one double bond in.
Step 4: Count in the product.
So the product still holds exactly one double bond, the carbonyl.
Step 5: Answer.
\[ \boxed{1} \]