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Chemistry 15 Online
OpenStudy (anonymous):

what alcohol is used in formation of this ester : BrCH2CH(OH)COO-CH(CH3)CH3 1)methanol 2)2-propanol 3)2-bromoethanol 4)3-bromo-1,2-propanediol

OpenStudy (abb0t):

I think it's 3. I'm having trouble seeing your structure.

OpenStudy (anonymous):

OH CH3 \ \ BrCH2CHCOO-CHCH3

OpenStudy (anonymous):

@abb0t THIS IS THE STRUCTURE

OpenStudy (preetha):

4

OpenStudy (abb0t):

Or 4. Lol

OpenStudy (anonymous):

could you tell me Why???

OpenStudy (abb0t):

I think it's because you have the alcohol on the primary which can be dehydrated and act as a nucleophile. I don't really remember ester synthesis too well.

OpenStudy (abb0t):

Sorry, not dehydrated, but you can remove the proton.

OpenStudy (anonymous):

thanks

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