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Write the IUPAC names of the following c...

Write the IUPAC names of the following compounds.
(i) `CH_(3)-CH_(2)-underset(OH)underset(|)(CH)-CH_(2)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(3)`
(ii) `CH-=C-CH=CH-CH=CH_(2)`

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(i)`implies` The functional group present is an alcohol {OH). Hence, the suffix is ‘-ol’, `implies` The longest chain containing -OH has eight carbon atoms. Hence, the corresponding saturated hydrocarbon is octane
`implies` The -OH is on carbon atom 3, In addition, a methyl group is attached at 6th carbon. Hence the IUPAC name is 6-Methyloctan-3-ol
(ii)The two C = C functional groups are present at carbon atoms 1 and 3, while the -C s C functional group is present at carbon 5. These groups are indicated by suffixes Hexa-1, 3-dien -5-yne.
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AAKASH INSTITUTE ENGLISH-ORGANIC CHEMISTRY : SOME BASIC PRINCIPLES AND TECHNIQUES -Assignment(Section-D)(Assertion - Reason Type Questions)
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  2. A: CH(3)-CH-CH(3) has 6. hyperconjugative hydrogens while CH(3)-CH-CH(...

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  3. A : Addition of HCN in alkene is a type of electrophilic substitution ...

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  4. A: The IUPAC name of CH(2)=CH-C=CH is but-3-en-1-yne. R: The prior...

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  5. A: Allyl carbanion (CH(2)=CH-CH(2)""^(-)) is more stable than""^(-)CH...

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  6. A: The isomeric structural alcohols of molecular formula C(4)H(10)O ar...

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  7. A:The formation of.NaCbTduring preparation q? sodium extract will give...

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  8. A : Before testing of halogens, sodium extract must be boiled with con...

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  9. A : Glycerol decomposes at its boiling point. R : It can be purifie...

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  10. Orthonitrophenol is steam volatile but paranitrophenol is not because ...

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  11. (a). If both (A) and (R) are correct and (R) is the correct explanatio...

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  12. A : Phenol is less acidic than benzoic acid. R: Phenoxide has less...

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  13. A : C(2)H(5) -""^(+)CH —C(2)H(5) . is more stable than CH(3)-""^(+)CH-...

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  14. A : CH(3)— BH — CH(2) can not show resonance. R : Boron and carboc...

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  15. A: C(2)BrClFI can form 6 different geometrical isomers. R : Each o...

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  16. A: Phenol is more reactive than toluene towards S(E) reaction. R: ...

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