Question

In the following carbocation, $$H/C{H_3}$$  that is most likely to migrate to the positively charged carbon is
General Organic Chemistry mcq question image

A. $$C{H_3}\,{\text{at}}\,C - 4$$
B. $$H\,{\text{at}}\,C - 4$$
C. $$C{H_3}\,{\text{at}}\,C - 2$$
D. $$H\,{\text{at}}\,C - 2$$  
Answer :   $$H\,{\text{at}}\,C - 2$$
Solution :
NOTE: Migrating tendency of hydride is greater than that of alkyl group. Further migration of hydride from $$C - 2$$   gives more stable carbocation ( stabilized by $$ + R$$  effect of $$OH$$ group and $$ + I$$  and hyper conjugative effects of methyl group ).
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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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