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Vadim26 [7]
3 years ago
13

Sodium ethanoate ? --> solid sodium ethanoate

Chemistry
1 answer:
timurjin [86]3 years ago
7 0
I’m pretty sure it craters sodium acetate
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See explanation

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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!

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