pKaH refers to the pKa of a leaving group's conjugate acid. The lower the value, the better a leaving group it is:
The leaving group ability of an anion depends on how stable it is at carrying negative charge. While pKa is the negative of a molecule's ability to dissociate into a proton and an anion. So this relation should also make sense intuitively.
Remember this is only a guide. For example, it does not factor in the stability of the carbonyl it creates by leaving.
The above table explains which group is pushed out in the attack below:
Great! Thank you :)
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