Question

The correct order of decreasing acidic strength of trichloroacetic acid $$(A),$$ trifluoroacetic acid $$(B),$$ acetic acid $$(C)$$ and formic acid $$(D)$$ is

A. $$B > A > D > C$$  
B. $$B > D > C > A$$
C. $$A > B > C > D$$
D. $$A > C > B > D$$
Answer :   $$B > A > D > C$$
Solution :
If an electron withdrawing group ( $$-I$$ - showing group ) is present, e.g. $$ - C{F_3}$$  has more ( $$-I$$ - effect ) withdrawing power than $$ - CC{l_3},$$  it makes the removal of proton more easy by stabilising the remaining carboxylate ion and thus, makes the acid more acidic.
The order of acidity of given compounds is
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Releted MCQ Question on
Organic Chemistry >> General Organic Chemistry

Releted Question 1

The bond order of individual carbon-carbon bonds in benzene is

A. one
B. two
C. between one and two
D. one and two alternately
Releted Question 2

Molecule in which the distance between the two adjacent carbon atoms is largest is

A. Ethane
B. Ethene
C. Ethyne
D. Benzene
Releted Question 3

Among the following, the compound that can be most readily sulphonated is

A. benzene
B. nitrobenzene
C. toluene
D. chlorobenzene
Releted Question 4

The compound 1, 2-butadiene has

A. only $$sp$$   hybridized carbon atoms
B. only $$s{p^2}$$ hybridized carbon atoms
C. both $$sp$$  and $$s{p^2}$$ hybridized carbon atoms
D. $$sp$$ , $$s{p^2}$$ and $$s{p^3}$$ hybridized carbon atoms

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