Why 1-position (-position) of naphthalene is more reactive than the 2-position (- position). Explain.

The greater reactivity of the 1-position (α-position) compared to the 2-position (β-position) in naphthalene can be attributed to several factors, including electronic effects, steric hindrance, and resonance stabilization.

Firstly, electronic effects play a significant role. At the 1-position, the carbon atom is directly attached to only one aromatic ring, while at the 2-position, it is attached ______ _________ _________ __________ _____ _________ __________ ____ ___ _____ _________ ___.
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