[hpl912]

I need help on this following reaction:



For the product 1), is it the attacking nucleophile the benzene ring with CO3H without the Cl? And i assume it replaces one of the H on the =CH2 terminal of the starting compound?

For the product 2), it looks like it's a hydroboration oxidation reaction? so the product should be having an OH replacing one of the H attached to the =CH2 terminal?
and if we continue the reaction with PCC and LDA (which i don't know this time what they do on the reaction), what are the resulting products?

thanks for any advice or help..

[macman104]

For reaction 1, google MCPBA.

For reaction 2, correct, it is hydroboration oxidation.
Then google "pyridinium chlorochromate" to see what happens for the next reaction.  I'm not exactly sure why they'd want you to add LDA afterwards though...