Advertisements
Advertisements
प्रश्न
Name the following compound according to the IUPAC system.
\[\begin{array}{cc}
\ce{CH3 - C = C - CH2OH}\\
|\phantom{......}|\phantom{.....}\\
\ce{CH3}\phantom{.}\ce{Br}\phantom{....}\\
\end{array}\]
Advertisements
उत्तर
2-Bromo-3-methylbut-2-en-1-ol
APPEARS IN
संबंधित प्रश्न
What is metamerism?
Explain metamerism with suitable examples of ethers
Write the IUPAC name of the following compound:
C6H5 – O – C2H5
Give the IUPAC name of the following ether:
Give the IUPAC name of the following ether:
What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?
Resorcinol on distillation with zinc dust gives _________.
Write IUPAC names of the following
3-methylphenol is called ____________.
One of the following is not a dihydroxy derivative of benzene.
1-Propanol and 2-propanol can be best distinguished by:
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
IUPAC name of the compound \[\begin{array}{cc}
\ce{CH3 - CH - OCH3}\\
\phantom{}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{..}
\end{array}\] is ______.
Which of the following compounds will react with sodium hydroxide solution in water?
Which of the following reagents can be used to oxidise primary alcohols to aldehydes?
(i) \[\ce{CrO3}\] in anhydrous medium.
(ii) \[\ce{KMnO4}\] in acidic medium.
(iii) Pyridinium chlorochromate.
(iv) Heat in the presence of Cu at 573 K.
Write the IUPAC name of the compound given below.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH2 - C = C - OH}\\
\phantom{........}|\phantom{....}|\phantom{}\\
\phantom{..............}\ce{CH3 CH2OH}
\end{array}\]
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.
Convert the following:
Ethyl alcohol into ethyl acetate.
Write the IUPAC name.
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]
