when grigngard reagent reacts with ketone it yields
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Nucleophilic Addition to C=O. Organolithium or Grignard reagents react with the carbonyl group, C=O, in aldehydes or ketones to give alcohols.
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These are reactions of the carbon-oxygen double bond, and so aldehydes and ketones react in exactly the same way - all that changes are the groups that happen to be attached to the carbon-oxygen double bond.
It is much easier to understand what is going on by looking closely at the general case (using "R" groups rather than specific groups) - and then slotting in the various real groups as and when you need to. The "R" groups can be either hydrogen or alkyl in any combination.
In the first stage, the Grignard reagent adds across the carbon-oxygen double bond:
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