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

Give IUPAC name of the following ether: CA2HA5OCHA2−CH−CHA3.....|.......CHA3 - Chemistry

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प्रश्न

Give IUPAC name of the following ether:

\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{CH3}
\end{array}\]

एक शब्द/वाक्यांश उत्तर
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उत्तर

1-Ethoxy-2-methylpropane

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

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

संबंधित प्रश्‍न

Name the following compound according to IUPAC system.


Write IUPAC name of the following compound:


Write IUPAC name of the following compound:

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


How is phenol converted into the following?

Benzene


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


Write IUPAC names of the following


Which of the following compounds is oxidised to prepare methyl ethyl ketone?


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


1-Propanol and 2-propanol can be best distinguished by:


The major product formed by the reaction:

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


IUPAC name of m-cresol is ______.


Arrange the following compounds in decreasing order of acidity.

\[\ce{H2O, ROH, HC ≡ CH}\]


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

Convert the following:

Ethyl alcohol into ethyl acetate.


How are the following conversions carried out?

Methyl magnesium bromide→2-Methylpropan-2-ol.


Draw structure of the following compound.

Prop-2-en-1-ol


Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.


Write IUPAC name of the following compound:

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


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