Answer:
<em>C. The electron-withdrawing fluorine atoms pull electron density from the oxygen in trifluoroacetate. The negative charge is more stabilized in trifluoroacetate by this effect.</em>
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Explanation:
<em>The structures of trifluoroacetate and acetic acid are both shown in the image attached.</em>
<em>The trifluoroacetate anion (CF3CO2-), just like the acetate anion has in the middle, two oxygen atoms.</em>
<em>However, in the trifluoroacetate anion, there are also three electronegative fluorine atoms attached to the nearby carbon atom attached to the carbonyl, and these pull some electron density through the sigma bonding network away from the oxygen atoms, thereby spreading out the negative charge further. This effect, called the "inductive effect" stabilizes the anion formed,the trifouoroacetate anion is thus more stabilized than the acetate anion.</em>
<em>Hence, trifluoroacetic acid is a stronger acid than acetic acid, having a pKa of -0.18.</em>
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<u><em>Hope this helps!</em></u>
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If two different elements combine separately with a fixed mass of a third element, the ratio of the masses in which they do so are either the same as or a simple multiple of the ratio of the masses in which they combine with each other.
