1 out of 3 attempts Select all that apply. a Assis Select all responses that exp

Question

1 out of 3 attempts Select all that apply. a Assis Select all responses that explain why the a of compound A is lower than pk Cheo the s of both compounds B and C. View CO2H Show O CO H CO Repor pKi 3.2 pK 3.9 pKa 4.4 .J A. The conjugate base of Cis more stable than the conjugate base of B. Compound A is less acidic than compounds B and C. Compound A has a stronger electron-donating inductive effect than both B and C. D. The o in A is more electronegative than the N in C. l E. Compound A has a stronger electron-withdrawing i effect than both B and C.

Explanation / Answer

Smaller tis the pKa higher is the acidic nature.

Higher si the acidic nature higher is the stability of conjugate base.

SO,

(D) The O in A is more electronegative than the N in C

(E) Compound A has a stronger electron withdrawing inductive effect than n both B and C

(G) The conjugate base of A is more stable than the conjugate base of C

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