Question

What is the decreasing order of strength of the bases $$O{H^ - },NH_2^ - ,HC \equiv {C^ - }$$     and $$C{H_3}CH_2^ - ?$$

A. $$C{H_3}CH_2^ - > NH_2^ - > HC \equiv {C^ - } > O{H^ - }$$  
B. $$HC \equiv {C^ - } > C{H_3}CH_2^ - > NH_2^ - > O{H^ - }$$
C. $$O{H^ - } > NH_2^ - > HC \equiv {C^ - } > C{H_3}CH_2^ - $$
D. $$NH_2^ - > HC \equiv {C^ - } > O{H^ - } > C{H_3}CH_2^ - $$
Answer :   $$C{H_3}CH_2^ - > NH_2^ - > HC \equiv {C^ - } > O{H^ - }$$
Solution :
Stronger the acid, weaker the conjugate base. Since acid character follows the order
$${H_2}O > HC \equiv CH > N{H_3} > C{H_3} - C{H_3}$$
( Acid character ),
the basic character of their conjugate bases decreases in the reverse order, i.e.,
$$C{H_3}CH_2^ - > NH_2^ - > HC \equiv {C^ - } > O{H^ - }$$
(Basic character)

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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