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प्रश्न
Write structural formulae for Cyclohex-2-en-1-ol.
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उत्तर
Cyclohex-2-en-1-ol
संबंधित प्रश्न
Explain metamerism with suitable examples of ethers
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:
\[\begin{array}{cc}
\ce{HO - CH2 - CH - CH2 - OH}\\
|\phantom{...}\\
\ce{OH}\phantom{.}\\
\end{array}\]
Write the IUPAC name of the following compound:
Write the IUPAC name of the following compound:
C6H5 – O – C2H5
Write the IUPAC name of the following compound:
C6H5 – O – C7H15(n−)
- Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names.
- Classify the isomers of alcohols in the above question as primary, secondary and tertiary alcohols.
What is the action of hot HI on it?
3-Methylbutane-2-ol on heating with HI gives ______
How is phenol converted into the following?
picric acid
Write structural formulae for 3-Methoxyhexane
Write IUPAC names of the following
In a carbinol system of nomenclature tert.butyl alcohol is named as _______________
Isopropyl alcohol on oxidation forms:
The compound HOCH2 – CH2OH is __________.
1-Propanol and 2-propanol can be best distinguished by:
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]
The product ‘Z’ is:
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 |
Identify A and B in the following:
Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
