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

Write the IUPAC name of the following compound: CH3 OH CH3

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प्रश्न

Write the IUPAC name of the following compound:

एक शब्द/वाक्यांश उत्तर
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उत्तर

2,5-Dimethylphenol

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पाठ 7: Alcohols, Phenols and Ethers - Exercises [पृष्ठ २२२]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 7 Alcohols, Phenols and Ethers
Exercises | Q 7.1 (vii) | पृष्ठ २२२

संबंधित प्रश्‍न

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.

\[\begin{array}{cc}
\ce{H2C = CH - CH - CH2 - CH2 - CH3}\\
|\phantom{...............}\\
\ce{OH}\phantom{............}
\end{array}\]


Write IUPAC name of the following compound:


Write the IUPAC name of the following compound:

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


Write the IUPAC name of the following compound:

C6H5 – O – C7H15(n−)


Give the IUPAC name of the following ether:

O2N – C6H4 – OCH3(p)


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?

benzoquinone


Propanoic acid to ethylamine.


Glycerol is ____________.


The compound HOCH2 – CH2OH is __________.


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


The IUPAC name of the ether CH2 = CH–CH2OCH3 is:


The heating of phenyl methyl ether with HI produces:


Match the structures of the compounds given in Column I with the name of the compounds given in Column II.

  Column I Column II
(i) (a) Hydroquinone
(ii) (b) Phenetole
(iii) (c) Catechol
(iv) (d) o-Cresol
(v) (e) guinone
(vi) (f) Resorcinol
    (g) Anisole

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: p-nitrophenol is more acidic than phenol.

Reason: Nitro group helps in the stabilisation of the phenoxide ion by dispersal of negative charge due to resonance.


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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