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CH(3)-CH(2)-CH(2)overset(OH)overset(|)CH...

`CH_(3)-CH_(2)-CH_(2)overset(OH)overset(|)CH_(2)` and `CH_(3)-underset(CH_(3))underset(|)overset(OH)overset(|)(OH)-CH_(3)`

A

chain isomers

B

positional isomers

C

both (a) and (b)

D

none of these

Text Solution

Verified by Experts

The correct Answer is:
a
When two compounds are chain isomers they can t be positional isomers.
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Explore conceptually related problems

Among these chain isomers are : (I) CH_(3)-CH_(3)-CH_(2)-CH_(2)-OH (II) CH_(3)-CH_(2)-underset(OH)underset(|)(CH)-CH_(3) (III) CH_(3)-underset(CH_(3))underset(|)overset(OH)overset(|)(C)-CH_(3)

Write the IUPAC name of the following compounds: (i) CH_(3)-underset(CH_(3))underset(|)(CH)-CO-underset(CH_(3))underset(|)(CH)-CH_(3) (ii) CH_(3)COCH_(2)COCH_(3) (iii) H_(3)C-overset(O)overset(||)(C)-CH_(2)-overset(Cl)overset(|)(CH)-CH_(3) (iv) CH_(3)-underset(OH)underset(|)(CH_(2))-overset(O)overset(||)(C)-CH_(3) (v)

Give the IUPAC names of the following : (i) CH_(3)-underset(OH)underset(|)(CH)-CH_(2)-Cl (ii) CH_(3)-CH_(2)-CH_(2)-underset(C_(6)H_(5))underset(|)overset(OH)overset(|)(C)-CH_(2)-CH_(3) (iii) CH_(3)-overset(OH)overset(|)(CH)-underset(CH_(3))underset(|)(CH)-CH_(3) (iv) CH_(3)-CH_(2)-overset(CH_(2)Cl)overset(|)(CH)-CH_(2)-OH (v) CH_(3)-CH_(2)-overset(CH_(2)OH)overset(|)(CH)-CH_(2)-CH_(3) (vi) CH_(3)-underset(OH)underset(|)(CH)-CH=CH_(2) (vii) CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-CH_(2)-OH (viii) CH_(3)-underset(Br)underset(|)overset(CH_(3))overset(|)(C)-underset(Br)underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-CH_(2)-OH (ix) CH_(3)-CH=CH-underset(OH)underset(|)(CH)-CH_(2)-CH_(3) (x) CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-underset(OH)underset(|)(CH)-CH_(3) (xi) CH_(3)-O-underset(CH_(3))underset(|)(CH)-CH_(3) (xii) CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-OH

The releative rate or acid catalyssed dehydration of following alcohols would be: (P) Ph-overset(CH_(3))overset(|)(C)-underset(OH)underset(|)(CH)-CH_(3) (Q) Ph-overset(CH_(3))overset(|)(C)-CH_(2)-CH_(2)-OH (R ) Ph--underset(OH)underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)CH_(3) Ph--underset(CH_(3))underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)OH

The releative rate or acid catalyssed dehydration of following alcohols would be: (P) Ph-overset(CH_(3))overset(|)(C)-underset(OH)underset(|)(CH)-CH_(3) (Q) Ph-overset(CH_(3))overset(|)(C)-CH_(2)-CH_(2)-OH (R ) Ph--underset(OH)underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)CH_(3) Ph--underset(CH_(3))underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)OH

H_(3)C-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH=CH_(2) to H_(3)C-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-underset(OH)underset(|)(CH)-CH_(3) . This change can be done by.

H_(3)C-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH=CH_(2) to H_(3)C-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-underset(OH)underset(|)(CH)-CH_(3) . This change can be done by.

Arrange the following in order of their reactivity toward decarboxylation reaction :- underset(I)(CH-=C overset(O)overset(||)C-OH) " "underset(II)(CH_(2)=CH-overset(O)overset(|)C-OH)" " underset(III)(CH_(3)-CH_(2)-overset(O)overset(||)C-OH) " " underset(IV)(CH_(3)-overset(CH_(3))overset(|)CH-overset(O)overset(||)C-OH)

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