Which of the following contributes to the higher electron density at ortho and para positions in an aromatic ether during electrophilic substitution?
Similar to phenols, where '-OH group directs the incoming group to ortho and para positions in the ring as these positions become electron rich due to the resonance effect caused by –OH group', the alkoxy group in ethers also shows a strong positive resonance effect, donating electron density to the ortho and para positions, thus activating them for electrophilic attack.