The following reactivity order has been found for the basic hydrolysis of p-substituted methyl benzoates: Y =
Question:
The following reactivity order has been found for the basic hydrolysis of p-substituted methyl benzoates: Y = NO2 > Br > H > CH3 > OCH3. How can you explain this reactivity order? Where would you expect Y = C ? N = Y = CHO, and Y = NH2 to he in the reactivity list?
Fantastic news! We've Found the answer you've been seeking!
Step by Step Answer:
A negatively charged tetrahedral intermediate is formed when the nucleoph...View the full answer
Answered By
Tamil Elakkiya Rajendran
I'm currently involved in the research in the field of Biothermodynamics, Metabolic pathway analysis and computational Biology. I always prefer to share my knowledge whatever I have learnt through my degree whenever time permits.
2+ Reviews
10+ Question Solved
Related Book For 
Question Posted:
