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Write IUPAC names of the following

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प्रश्न

Write IUPAC names of the following

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उत्तर

2-Nitrophenol

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  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 11: Alcohols, Phenols and Ethers - Exercises [पृष्ठ २५३]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
अध्याय 11 Alcohols, Phenols and Ethers
Exercises | Q 6.3 | पृष्ठ २५३

वीडियो ट्यूटोरियलVIEW ALL [3]

संबंधित प्रश्न

What is metamerism? 


Name the following compound according to the IUPAC system.

\[\begin{array}{cc}
\phantom{..................}\ce{CH2OH}\\
\phantom{.........}|\\
\ce{CH3 - CH2 - CH - CH - CH - CH3}\\
\phantom{.........}|\phantom{...................}|\\
\phantom{.............}\ce{CH2Cl}\phantom{..........}\ce{CH3}\phantom{}
\end{array}\]


Name the following compound according to the IUPAC system.

\[\begin{array}{cc}
\phantom{.....................................}\ce{CH2OH}\\
\phantom{............................}|\\
\ce{CH3 - CH - CH2 - CH - CH - CH3}\\
|\phantom{....................}|\phantom{............}\\
\ce{CH3}\phantom{..............}\ce{OH}\phantom{.........}\\
\end{array}\]


Write the IUPAC name of the following compound:


Give the IUPAC name of the following ether:


Which of the following compounds is NOT prepared by the action of alcoholic NI3 on alkyl halide?

(a) CH3NH2

(b) CH3- CH2- NH2

(c) CH3 - CH2 - CH2 - NH2

(d) (CH3)C- NH2


How is phenol converted into the following?

picric acid


Write the structures of the products when Butan-2-ol reacts with CrO3


Write the structures of the products when Butan-2-ol reacts with SOCl2


How do you convert the Ethanal to Propanone


What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?


Propanoic acid to ethylamine.


Write structural formulae for 1-Ethylcyclohexanol.


Write structural formulae for Cyclohex-2-en-1-ol.


Isopropyl alcohol on oxidation forms:


Give IUPAC names of the following compound:

\[\begin{array}{cc}
\phantom{..}\ce{H}\phantom{...}\ce{CH3}\phantom{.}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\ce{H - C - C - C - H}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\phantom{.}\ce{H}\phantom{...}\ce{OH}\phantom{.}\ce{H}\phantom{.}\\
\end{array}\]


C6H5OCH2CH3 is called:


Butane-2-ol is ____________.


The major product formed by the reaction:

\[\begin{array}{cc}
\ce{CH3CH-CH2Br ->[CH3O^-][CH3OH] is}\\
|\phantom{................}\\
\ce{CH3}\phantom{.............}
\end{array}\]


\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]


Which of the following compounds will react with sodium hydroxide solution in water?


What happens when benzene diazonium chloride is heated with water?


Explain why p-nitrophenol is more acidic than phenol.


Match the starting materials given in Column I with the products formed by these (Column II) in the reaction with HI.

  Column I   Column II
(i) CH3—O—CH3 (a)
(ii) \[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
\backslash\phantom{.............}\\
\ce{CH-O-CH3}\\
/\phantom{..............}\\
\ce{CH3}\phantom{..................}
\end{array}\]
(b) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-I + CH3OH}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]
(iii) \[\begin{array}{cc}
\ce{CH3}\phantom{.}\\
|\phantom{....}\\
\ce{H3C-C-O-CH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]
(c)
(iv) (d) CH3—OH + CH3—I
    (e) \[\begin{array}{cc}
\ce{CH3}\phantom{.....................}\\
\backslash\phantom{.................}\\
\ce{CH-OH + CH3I}\\
/\phantom{.................}\\
\ce{CH3}\phantom{.....................}
\end{array}\]
    (f) \[\begin{array}{cc}
\ce{CH3}\phantom{.....................}\\
\backslash\phantom{.................}\\
\ce{CH-I + CH3OH}\\
/\phantom{.................}\\
\ce{CH3}\phantom{.....................}
\end{array}\]
    (g) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-OH + CH3I}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]

Assertion: Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.

Reason: Lewis acid polarises the bromine molecule.


Explain why Lewis acid is not required in bromination of phenol?


Write IUPAC name of the following compound:

\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]


Draw structure of the following compound.

2-Methoxypropane


Write the IUPAC name.

\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C  -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]


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