Question

$$But$$  $$-2-ene$$   exhibits $$cis-trans-isomerism$$      due to

A. rotation around $${C_2} - {C_3}$$  double bond
B. rotation around $${C_3} - {C_4}$$  sigma bond
C. rotation around $${C_1} - {C_2}$$  bond
D. restricted rotation around $$C=C$$  bond  
Answer :   restricted rotation around $$C=C$$  bond
Solution :
Due to presence of $$ > C = C < $$   in $$but$$  $$-2-ene,$$   it shows restricted rotation. Hence, give two types of arrangements around the space of $$ > C = C < $$   as $$cis$$  and $$trans$$  - forms.

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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