how do you account for the difference in acidity between meta and para methoxyphenol?
acidity is essentially due to the ability to "lose" or "donate" a Hydrogen ion as H+ in solution
this is due to electronegativity difference
this is due to forces of electrons and protons interacting between each other in repulsion and attractions
The force depends on:
- charge
- distance
position of meta and para are clearly different length away
therefore
para has the "farther" position as meta
therefore, expect less interaction
less interaction, less force, less force less electronegativity difference
less electornegativity difference, less posibility of polarizing with H+
therefore, less acidic
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