Answer:
Step-by-step explanation:
We see that The aldehyde reacts with water and forms gem-diols.
The electron withdrawing groups destabilizes the carbonyl . Fluorine being more electronegative removes more electron density from the carbonyl carbon, thus destabilizing the carbon and allowing for more gem-diol to form and tends to form stable gem-diol. As well, the carbonyl carbon becomes more electrophilic.
Therefore, the following statements are true regarding the fluorinated aldehyde.
"The hydrate form is favored over the carbonyl."
"There will be more geminal double hydroxyl form than carbonyl."
"The carbonyl carbon is more activated to hydrate formation in the fluorinated derivative compared to the non-fluorinated analog."
"There will be more of the gem-diol than carbonyl."
NB: uploaded image to describe the explanation clearly.
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