The abovefirst compound is said to be hydrolisedhydrolyzed more easily than thisthe 2nd compound below under Alkaline medium . How is this possible ? 
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I thought due to resonance NO2, -NO2 acquires negative charge which facesfaces repulsion from the solvation effect by basic medium. But it will be relatively easier for oxygen in ch3o-CH3O( in 2nd compound) to donate its electrons to have it in resonance with benzene. But this contradicts with answer. Where am iI going wrong?
The above compound is said to be hydrolised more easily than this under Alkaline medium . How is this possible ?
I thought due to resonance NO2 acquires negative charge which faces repulsion from the solvation effect by basic medium. But it will be relatively easier for oxygen in ch3o( in 2nd compound) to donate its electrons to have it in resonance with benzene. But this contradicts with answer. Where am i going wrong?
The first compound is said to be hydrolyzed more easily than the 2nd compound below under Alkaline medium . How is this possible ?
I thought due to resonance, -NO2 acquires negative charge which faces repulsion from the solvation effect by basic medium. But it will be relatively easier for oxygen in -CH3O( in 2nd compound) to donate its electrons to have it in resonance with benzene. But this contradicts with answer. Where am I going wrong?
The above compound is said to be hydrolised more easily than this under Alkaline medium . How is this possible ?
I thought due to resonance NO2 acquires negative charge which faces repulsion from the solvation effect by basic medium. But it will be relatively easier for oxygen in ch3o( in 2nd compound) to donate its electrons to have it in resonance with benzene. But this contradicts with answer. Where am i going wrong?
