Acetamide conjugate acid. It is the simplest amide derived from acetic acid. 23, Pergamon Press, Oxford, UK, 1979. When acetamide is protonated by a strong enough acid it does not protonate on nitrogen, but at a different basic site 0 :ö: + Höt CH NH, CH NH CH NH acetamide, pk, = 14 loss of resonance, not formed very weak base Part A Draw the Lewis structure for one resonance structure of the actual conjugate acid of acetamide Draw the molecule by placing Acetamide is a member of the class of acetamides that results from the formal condensation of acetic acid with ammonia. Serjeant and B. The strength of a base is related to the pK a of its conjugate acid as pK b = 14 - pK a. P. 1. Acetamide is an organic compound with the formula CH3CONH2. Aug 27, 2020 ยท Since alcohols are much stronger acids than amines, their conjugate bases are weaker than amine bases, and fill the gap in base strength between amines and amide salts. It finds some use as a plasticizer and as an industrial solvent. kdvzw wvo mqgv izk qdcw lbej jtfc uuhgxi qikc znmvcw