Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: Mmm1233 on October 24, 2019, 11:17:11 AM
-
Why does the P-methoxybezyl chloride follow SN1 reaction mechanism with methanol while P-nitrobezyl bromide follows SN2 reaction mechanism?
-
Can you draw the cation intermediat for p-methoxybenzyl bromide reaction? Can you draw a similar resonance stabilized cation for the p-nitrobenzyl bromide?
-
Think about the influence of the substituents on the cation.