The correct order of acidic strength of the given carboxylic acids will be decided by the stability of their conjugate bases. The +I effect of CH3 group destabilises the carboxylate anion. But the −I effect of halogen substituted methyl group stabilises the carboxylate anion. Higher the −I effect of the halogen substituted methyl group, higher the acidic strength of the corresponding acid.
∴ Correct order of acidic strength is
F3C− (B) COOH>FCH2− (D) COOH>(C)CICH2−COOH>(E)BrCH2−COOH>(A)CH3−COOH