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प्रश्न
Write IUPAC name of the following
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उत्तर
1-Methylcyclopentanol
APPEARS IN
संबंधित प्रश्न
Name the following compound according to the IUPAC system.
\[\begin{array}{cc}
\ce{H2C = CH - CH - CH2 - CH2 - CH3}\\
|\phantom{...............}\\
\ce{OH}\phantom{............}
\end{array}\]
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:
\[\begin{array}{cc}
\ce{HO - CH2 - CH - CH2 - OH}\\
|\phantom{...}\\
\ce{OH}\phantom{.}\\
\end{array}\]
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - O - CH2 - CH - CH3}\\
\phantom{................}|\\
\phantom{....................}\ce{CH3}
\end{array}\]
Give the IUPAC name of the following ether:
CH3CH2CH2OCH3
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)3 C- NH2
3-Methylbutane-2-ol on heating with HI gives ______
How is phenol converted into the following?
benzoquinone
Write the structures of the products when Butan-2-ol reacts with SOCl2
Write the IUPAC name of the following :
How do you convert the Ethanal to Propanone
Isopropyl alcohol on oxidation forms:
Butane-2-ol is ____________.
When ethyl alcohol reacts with acetic acid, the products formed are:
1-Propanol and 2-propanol can be best distinguished by:
\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]
The product ‘Z’ is:
IUPAC name of the compound is:
\[\begin{array}{cc}
\ce{CH3-CH-OCH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]
Explain why p-nitrophenol is more acidic than phenol.
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: Phenol forms 2, 4, 6 – tribromophenol on treatment with \[\ce{Br2}\] in carbon disulphide at 273 K.
Reason: Bromine polarises in carbon disulphide.
How can phenol be converted to aspirin?
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
Write structural formulae for:
p-Nitrophenol
Write structural formulae for:
Salicylic acid
The IUPAC name of 
is ______.
