Mechanism of aspirin by salicyclic acid reacts with acetic acid ? Mechanism of benzoic acid from benzamide?

See explanation

Explanation:

The synthesis of aspirin is shown in the reaction scheme attached to this answer. The production of aspirin involves the reaction of acetyl salicyclic acid and acetic anhydride. HA in the reaction mechanism refers to an acid that is used in the reaction

Similarly  benzamide, is converted to the carbonyl carbocation by reaction with acid. The -NH2 group is protonated and subsequently departs as a leaving group. An OH^- completes the mechanism forming a carboxylic acid. The movement of electrons is shown in the image attached.

Again, the diazotization of benzamide using sodium nitrate and concentrated HCl yields benzene diazonium chloride. Addition of water to benzene diazonium chloride yields the benzoic acid and nitrogen gas.

pie chart because it is in percents ( % )

the correct answer is b. a strong acid completely dissociates to its ions when dissolved in water. completely dissociates to and ions. a is incorrect because does not fully ionize to and ions and some remain as the compound . c and d are incorrect because, and do not fall into the category of bronsted lowry acids. a bronsted lowry acid is a proton donor and since both molecules do not have a proton to donate they are not bronsted lowry acids. likewise,   if we use the lewis acid definition, they cannot be acids. a lewis acid is an electron pair acceptor. both and have a complete octet so can not accept any electrons which disqualifies them as acids.