arrange athe following in increasing order pf acidic strength:`CICH_2COOH,CH_3CH2COOH,FCH_2COOH`

Carboxylic acids are distinctly acidic and ionise in water to give H_3 O^+ ions. In general, electron withdrawing groups increase the acidity of carboxylic acids while electron donating groups decrease the acidity of the carboxylic acid. The electron releasing groups such as -CH_3 -OH, -NH_2 and -OCH_3 make benzoic acid weaker while electron withdrawing groups such as -CI, -NO_2 , etc., make benzoic acid stronger. The ortho isomer of every substituted benzoic acid is the strongest among the three isomers due to effect known as ortho effect. Carboxylic acids neutralise alkalies, decompose carbonates and bicarbonates evolving CO_2 with brisk effervescence. Arrange the following in increasing order of acidic strength : FCH_2 COOH ,CH_3 COOH, CICH_2 COOH ,CH_3 CH_2 OH ,C_6 H_5 COOH

Arrange the following in increasing order of acidic strength: ClCH_(2)COOH, CH_(3)CH_(2)COOH, ClCH_(2)CH_(2)COOH, CH_(3)COOH .

Arrange the following in increasing order of acidic strength : (CH_(3))_(2)CHCOOH(I),CH_(3)CH_(2)CH(Br)COOH(II),CH_(3)CH(Br)CH_(2)COOH(III)

Arrange the following in the increasing order of acidic strength : (i) ClCH_2 COOH (ii) CH_2 ClCH_2 COOH (iii ) FCH_2 COOH (iv) CH_3 COOH

Arrange the following in increasing order of acid strength : (i) CH_(3)CH_(2)CH(Br)COOH , (ii) CH_(3)CH(Br)CH_(2)COOH , (iii) CH_(3)COOH

Arrange the following in order of increasing acidic strength (i) HCOOH,ClCH_(2)COOH,CH_(3)COOH (ii) CH_(3)COOH,(CH_(3))_(2)CHCOOH,(CH_(3))_(3)CCOOH (iii) ClCH_(2)COOH,Cl_(2)CHCOOH,ClCl_(3)C.COOH (iv) ClCH_(2)COOH,CH_(3)CH_(2)COOH,ClCH_(2)CH_(2)COOH,(CH_(3))_(2)CH.COOH,CH_(3)COOH.

Arrange the following in increasing order of esterification: HCOOH,CH_(3)COOH,CH_(3)CH_(2)COOH,CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)(C)-COOH

Arrange the following in the decresing order of acidic strength : (a) H_2 O , CH_3 OH , C_6 H_5 ,OH ,CH _2 COOH (b) CH_3 CH_2 COOH ,HOCH, C_6 H_5COOH ,ClCH_2 COOH