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प्रश्न
Write the IUPAC name of the following compound:
C6H5 – O – C7H15(n−)
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उत्तर
1-Phenoxyheptane
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संबंधित प्रश्न
What is metamerism?
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{........................}\ce{CH3}\\
\phantom{....................}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.........}|\phantom{.........}|\\
\phantom{...}\ce{CH3}\phantom{....}\ce{OH}\phantom{....}\ce{CH3}\\
\end{array}\]
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{HO - CH2 - CH - CH2 - OH}\\
|\phantom{...}\\
\ce{OH}\phantom{.}\\
\end{array}\]
Give the IUPAC name of the following ether:
\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.........}|\\
\phantom{.............}\ce{CH3}
\end{array}\]
Give the IUPAC name of the following ether:
CH3OCH2CH2Cl
Give the IUPAC name of the following ether:
Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.
(A) formaldehyde
(B) acetaldehyde
(C) acetone
(D) ethyl methyl ketone
Give reasons Fluoride ion has higher hydration enthalpy than chloride ion.
Write the IUPAC name of the following :
One of the following is not a dihydroxy derivative of benzene.
IUPAC name of m-cresol is ____________.
1-Propanol and 2-propanol can be best distinguished by:
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
Among the following sets of reactants which one produces anisole?
Explain why p-nitrophenol is more acidic than phenol.
Assertion: IUPAC name of the compound
\[\begin{array}{cc}
\ce{CH3 - CH - O - CH2 - CH2 - CH3}\\
|\phantom{....................}\\
\ce{CH3}\phantom{.................}
\end{array}\] is 2-Ethoxy-2-methylethane.
Reason: In IUPAC nomenclature, ether is regarded as hydrocarbon derivative in which a hydrogen atom is replaced by —OR or —OAr group [where R = alkyl group and Ar = aryl group]
How can phenol be converted to aspirin?
Draw structure of the following compound.
2. 5-Diethylphenol
Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.
Write the IUPAC name.
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]
