Among -NR2 and -NH2 which activates the benzene ring to a greater extent? What is the reason for that?

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Explain the fact that in aryl alkyl ethers
The alkoxy group activates the benzene ring towards electrophilic substitution.

It directs the incoming substituents to ortho and para positions in benzene ring.

What is meant by activating or deactivating a benzene ring?

(- N H_{2}, - N R_{2}, - N H R)

- {N H}_{2}

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