Question

Base strength of
$$\eqalign{ & \left( {\text{i}} \right)\,{H_3}C\mathop C\limits^\Theta \,{H_2} \cr & \left( {{\text{ii}}} \right)\,{H_2}C = \mathop C\limits^\Theta H \cr & \left( {{\text{iii}}} \right)H - C \equiv \mathop C\limits^\Theta \cr} $$
is in the order of

A. (ii) > (i) > (iii)
B. (iii) > (ii) > (i)
C. (i) > (iii) > (ii)
D. (i) > (ii) > (iii)  
Answer :   (i) > (ii) > (iii)
Solution :
Weaker the acid, stronger is its conjugate base. Among alkane, alkene and alkyne, alkynes are most acidic and alkanes are least acidic, so the order of base strength is
$$\eqalign{ & alkane > alkene > \,alkyne\,\,\,\,\,\,{\text{or}} \cr & C{H_3}\mathop C\limits^\Theta {H_2} > {H_2}C = \mathop C\limits^\Theta H > H - C \equiv \mathop C\limits^\Theta \cr} $$

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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