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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Give IUPAC name of the following ether: OC2H5 - Chemistry

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प्रश्न

Give IUPAC name of the following ether:

एक शब्द/वाक्यांश उत्तर
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उत्तर

Ethoxybenzene

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अध्याय 7: Alcohols, Phenols and Ethers - Exercises [पृष्ठ २२४]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 7 Alcohols, Phenols and Ethers
Exercises | Q 7.23 (vi) | पृष्ठ २२४

संबंधित प्रश्न

Explain metamerism with suitable examples of ethers


Write IUPAC name of the following compound:

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


Write structures of the compounds whose IUPAC names are as follows:

3-Chloromethylpentan-1-ol.


Give IUPAC name of the following ether:

CH3CH2CH2OCH3


Write the IUPAC name of the following :


Resorcinol on distillation with zinc dust gives _________.


Glycerol is ____________.


3-methylphenol is called ____________.


The compound HOCH2 – CH2OH is __________.


An example of a compound with functional group – O – is ____________.


Butane-2-ol is ____________.


Cresol has ____________.


Ethyl alcohol is industrially prepared from ethylene by:


Among the following sets of reactants which one produces anisole?


Give IUPAC name of the compound given below.

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


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) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-OH + CH3I}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]

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


Write the IUPAC name of the following compound.


Identify A and B in the following:


Write the IUPAC name of the following compound:

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


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