The increasing order of pK for the following compounds will be : i) H N–CH=NH ii) iii) CH NHCH b 2 3 — Amines Chemistry Question
Question
The increasing order of pK for the following compounds will be : i) H N–CH=NH ii) iii) CH NHCH b 2 3 3 2 o 3 b (A) ii < iii < i (B) iii < i < ii (C) i < ii < iii (D) ii < i < iii
💡 Solution & Explanation
Weaker the conjugate acid, stronger the base. (ii) is the most basic as it has a guanidine like Structure. It has a high tendency of accepting a proton, giving rise to a very stable conjugate acid and hence, is a very strong base.In compound (i), the N is sp hybridised and its electronegativity is higher as compared to the compound (iii) which is a 2 amine (sp hybridised). So compound (ii) is more basic compared to compound (iii). So the order of basicity is ii > i > iii and thus the order of pK value will be iii > i > ii