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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.Oh, this one I can help.
First, form a Grignard reagent.
Grignard reagent produces a carbanion that attacks formaldehyde. You get a primary alcohol, with a -CH2OH replacing the Br.
The acidic medium is deprotection. You get an aldehyde on the left end.
Option C looks about right.
yeah its right but i didnt get the aldehyde part
oh right
its just the reverse of acetal formation
danks
+solved @Opt
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