What is the best  rationale for the difference in acidity in acetone and diethyl ether? A. The more acidic compound has a hydrogen attached to a more electronegative atom B. The more acidic compound has a hydrogen attached to a larger atomic radius atom C.  The more acidic compound has a more stable conjugate base because of addition resonance structures stabilizing the charge D. The more acidic compound has a stronger molecular dipole that increases the polarization of the acidic hydrogen E. The more acidic compound has a greater amount of s-character in the acidic bond.

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What is the best  rationale for the difference in acidity in acetone and diethyl ether?

A. The more acidic compound has a hydrogen attached to a more electronegative atom

B. The more acidic compound has a hydrogen attached to a larger atomic radius atom

C.  The more acidic compound has a more stable conjugate base because of addition resonance structures stabilizing the charge

D. The more acidic compound has a stronger molecular dipole that increases the polarization of the acidic hydrogen

E. The more acidic compound has a greater amount of s-character in the acidic bond.

+)
H.
+)
acetone
diethyl ether
:
Transcribed Image Text:+) H. +) acetone diethyl ether :
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