Why maleic acid is more acidic than fumaric acid, on the basis of dipole moment
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Maleic acid or cis- butenedioic acid, being a cis- isomer is capable of forming intra-hydrogen bond after losing H+ ion, making the conjugate Base (negative ion) much stable than the trans form (Fumaric acid) because both the oxygen atoms have strong interaction with the remaining H atom.
Consider the reaction,
Ha + H2O <=>H3O+ + A-
If the conjugate Base is being more stable, equilibrium shifts mainly to the right to provide more H+ ions, and thus increases the rate of reaction.
However, fumaric acid would not have this stabilisation and thus less H+ ion is produced.
Hope this helps u!
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