Carbonyl compounds can be protonated on the carbonyl oxygen. Explain why butanoic acid is more readily protonated than butanone.

Idon't know hope someone you

Answerit curves up and levels out.explanationwe assume that the container contains absolutely no ammonia to begin with as it states that "nitrogen gas and hydrogen gas" react to "produce ammonia."at dynamic equilibrium, the product and reactant concentrations are equal.this means that, starting from a concentration of zero, [nh₃] must curve "up" from zero and then level out to a constant concentration.

Hi + naoh -> h2o + nal

The answer you are looking for is option d