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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

उत्तर

Ethoxybenzene

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पाठ 11: Alcohols, Phenols and Ethers - Exercises [पृष्ठ ३४६]

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एनसीईआरटी Chemistry [English] Class 12
पाठ 11 Alcohols, Phenols and Ethers
Exercises | Q 23.6 | पृष्ठ ३४६

संबंधित प्रश्‍न

Write IUPAC name of the following compound:

\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
\phantom{}|\phantom{.............}|\phantom{......}|\phantom{.........}\\
\phantom{}\ce{OH}\phantom{..........}\ce{OH}\phantom{...}\ce{C2H5}\phantom{......}
\end{array}\]


  1. Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names.
  2. Classify the isomers of alcohols in the above question as primary, secondary and tertiary alcohols.

Natalite is a mixture of

(a) diethyl ether and methanol

(b) diethyl ether and ethanol

(c) dimethyl ether and methanol

(d) dimethyl ether and ethanol


3-Methylbutane-2-ol on heating with HI gives ______


How is phenol converted into the following?

benzene


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


Give IUPAC names of the following compound:


C6H5OCH2CH3 is called:


One of the following is not a dihydroxy derivative of benzene.


HBr reacts fastest with ____________.


Ethylene reacts with Baeyer’s reagent to give ______.


When ethyl alcohol reacts with acetic acid, the products formed are:


The heating of phenyl methyl ether with HI produces:


IUPAC name of the compound is:

\[\begin{array}{cc}
\ce{CH3-CH-OCH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]


IUPAC name of m-cresol is ______.


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


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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