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Question

Compound with molecular formula C3H6O can show-


A

Both positional isomerism and metamerism

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B

Metamerism

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C

Positional isomerism

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D

Functional group isomerism

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Solution

The correct option is D

Functional group isomerism


Explanation for the correct option:

(D) For a compound with the molecular formula CcHhXxNnOo

Degree of unsaturation =(C+1)-H2-X2+N2

Where, X=Halogen

C=NumberofcarbonatomH=NumberofhydrogenatomN=NumberofnitrogenatomO=Numberofofoxygenatom

In C3H6O

Degree of saturation=(3+1)-62=1

Degree of saturation=1

Possible functional group isomers are CH3-CH2-CH=O(propanone)&CH3-CO-CH3(propanal).

Therefore, functional group isomerism is the most appropriate.

Explanation for incorrect options:

(B) Metamerism has different alkyl chain groups around the functional group.

(C) Positional isomerism arises due to to a difference in the position of the substituent atom or a functional group on the carbon skeleton.

(A) From the above information, we can see that both metamerism and positional isomers are not possible.

Hence, the correct option is (D).


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