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tanrabbit20Lv1
6 Nov 2019
Select all responses that explain why the pKa of compound A is lower than the pKa's of both compounds B and C. Compound A has a stronger electron-withdrawing inductive effect than both B and C. The O in A is more electronegative than the N in C. The conjugate base of C is more stable than the conjugate base of A. Compound A has a stronger electron-donating inductive effect than both B and C. The conjugate base of A is more stable than the conjugate base of C. Compound A is less acidic than compounds B and C. The O in compound A is closer to the COOH group than the O in B. Show transcribed image text
Select all responses that explain why the pKa of compound A is lower than the pKa's of both compounds B and C. Compound A has a stronger electron-withdrawing inductive effect than both B and C. The O in A is more electronegative than the N in C. The conjugate base of C is more stable than the conjugate base of A. Compound A has a stronger electron-donating inductive effect than both B and C. The conjugate base of A is more stable than the conjugate base of C. Compound A is less acidic than compounds B and C. The O in compound A is closer to the COOH group than the O in B.
Show transcribed image text Keith LeannonLv2
12 Sep 2019