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प्रश्न
Write the IUPAC name of the following compound:
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उत्तर
2,6-Dimethylphenol
APPEARS IN
संबंधित प्रश्न
Name the following compound according to the IUPAC system.
\[\begin{array}{cc}
\ce{H2C = CH - CH - CH2 - CH2 - CH3}\\
|\phantom{...............}\\
\ce{OH}\phantom{............}
\end{array}\]
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{........................}\ce{CH3}\\
\phantom{....................}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.........}|\phantom{.........}|\\
\phantom{...}\ce{CH3}\phantom{....}\ce{OH}\phantom{....}\ce{CH3}\\
\end{array}\]
Give the IUPAC name of the following ether:
O2N – C6H4 – OCH3(p)
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
How is phenol converted into the following?
benzoquinone
How is phenol converted into the following?
picric acid
Write IUPAC name of the following compound (CH3)2 N − CH2CH3
Write the IUPAC name of the following compound:
What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?
The compound HOCH2 – CH2OH is __________.
HBr reacts fastest with ____________.
When ethyl alcohol reacts with acetic acid, the products formed are:
1-Propanol and 2-propanol can be best distinguished by:
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 |
How can phenol be converted to aspirin?
Write a chemical reaction for the following conversion:
Acetic acid into ethyl alcohol.
Draw structure of the following compound.
2. 5-Diethylphenol
Draw structure of the following compound.
Prop-2-en-1-ol
Write structural formulae for:
Salicylic acid
Write the IUPAC name.
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]
