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Answer:
See explanation
Explanation:
For this question, we have to remember the effect of an atom with high <u>electronegativity</u> as "Br". If the "Br" atom is closer to the carboxylic acid group (COOH) we will have an <u>inductive effect</u>. Due to the electronegativity of Br, the electrons of the C-H bond would be to the Br, then this bond would be <u>weaker</u> and the compound will be more acid (because is easier to produce the hydronium ion ).
With this in mind, for A in the last compound, we have <u>2 Br atoms</u> near to the acid carboxylic group, so, we will have a high inductive effect, then the C-H would be weaker and we will have <u>more acidity</u>. Then we will have the compound with only 1 Br atom and finally, the last compound would be the one without Br atoms.
In B, the difference between the molecules is the <u>position</u> of the "Br" atom in the molecule. If the Br atom is closer to the acid group we will have a <u>higher inductive effect</u> and more <u>acidity</u>.
See figure 1
I hope it helps!
