हिंदी

In a carbinol system of nomenclature tert.butyl alcohol is named as _______________

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प्रश्न

In a carbinol system of nomenclature tert.butyl alcohol is named as _______________

विकल्प

  • trimethyl carbinol

  • dimethyl ethyl carbinol

  • methyl carbinol

  • ethyl carbinol

MCQ
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उत्तर

In a carbinol system of nomenclature tert.butyl alcohol is named as trimethyl carbinol

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अध्याय 11: Alcohols, Phenols and Ethers - Multiple choice questions

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एससीईआरटी महाराष्ट्र Chemistry [English] Standard 12 Maharashtra State Board
अध्याय 11 Alcohols, Phenols and Ethers
Multiple choice questions | Q 1

वीडियो ट्यूटोरियलVIEW ALL [3]

संबंधित प्रश्न

Write the IUPAC name of the given compound:


Name the following compound according to the IUPAC system.

\[\begin{array}{cc}
\ce{CH3 - C = C - CH2OH}\\
|\phantom{......}|\phantom{.....}\\
\ce{CH3}\phantom{.}\ce{Br}\phantom{....}\\
\end{array}\]


Write the IUPAC name of the following compound:

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


Write the IUPAC name of the following compound:

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


Give the IUPAC name of the following ether:

O2N – C6H4 – OCH3(p)


Give the IUPAC name of the following ether:


Give reasons Fluoride ion has higher hydration enthalpy than chloride ion.


How do you convert the Ethanal to Propanone


Propanoic acid to ethylamine.


Write structural formulae for 1-Ethylcyclohexanol.


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


Write IUPAC names of the following


Give IUPAC names of the following compound:

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


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


Ethyl alcohol is industrially prepared from ethylene by:


n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent?


The heating of phenyl methyl ether with HI produces:


\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]

The product ‘Z’ is:


IUPAC name of the compound is:

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


The correct acidic strength order of the following is:


     (I)


    (II)


     (III)


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

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


How can phenol be converted to aspirin?


The IUPAC name of is ______.


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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