1. The following reactivity order has been found for the basic hydrolysis of p-substituted methyl benzoates: Y= NO2 > Br> H>CH3 >OCH3 .CO2CH3 .co OH + CH,OH H,0 How can you explain this reactivity order? Where would you expect Y=CEM Y = CHO, and Y = NH2 to be in the reactivity list?

1. The following reactivity order has been found for the basic hydrolysis of p-substituted methyl benzoates: Y= NO2 > Br> H>CH3 >OCH3 .CO2CH3 .co OH + CH,OH H,0 How can you explain this reactivity order? Where would you expect Y=CEM Y = CHO, and Y = NH2 to be in the reactivity list?

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter20: Carboxylic Acids And Nitriles

Section20.SE: Something Extra

Problem 25MP: Acid-catalyzed hydrolysis of a nitrile to give a carboxylic acid occurs by initial protonation of...

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Question

Answer the question in the picture

1. The following reactivity order has been found for the basic hydrolysis of
p-substituted methyl benzoates:
Y= NO2 > Br>H>CH3 > OCH3
.CO2CH3
OH
+ CH,OH
H,0
How can you explain this reactivity order? Where would you expect Y=CEN
Y= CHO, andY= NH2 to be in the reactivity list?|

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