Advertisements
Advertisements
प्रश्न
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - CH - CH - CH3}\\
|\phantom{.........}|\phantom{...}\\
\ce{OH}\phantom{....}\ce{OH}\\
\end{array}\]
Advertisements
उत्तर
Butane-2,3-diol
APPEARS IN
संबंधित प्रश्न
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 structure and IUPAC name of 'methyl-n-propyl ether'.
How do you convert the Ethanal to Propanone
Write structural formulae for 3-Methoxyhexane
Write a structural formula for methyl vinyl ether.
Write structural formulae for Cyclohex-2-en-1-ol.
Isopropyl alcohol on oxidation forms:
Give IUPAC names of the following compound:
\[\begin{array}{cc}
\phantom{..}\ce{H}\phantom{...}\ce{CH3}\phantom{.}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\ce{H - C - C - C - H}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\phantom{.}\ce{H}\phantom{...}\ce{OH}\phantom{.}\ce{H}\phantom{.}\\
\end{array}\]
3-methylphenol is called ____________.
The compound HOCH2 – CH2OH is __________.
Which of the following compounds is oxidised to prepare methyl ethyl ketone?
1-Propanol and 2-propanol can be best distinguished by:
Which of the following gives a positive iodoform test?
The correct acidic strength order of the following is:
(I)
(II)
(III)
Write steps to carry out the conversion of phenol to aspirin.
Explain why p-nitrophenol is more acidic than phenol.
Assertion: Phenol forms 2, 4, 6 – tribromophenol on treatment with \[\ce{Br2}\] in carbon disulphide at 273 K.
Reason: Bromine polarises in carbon disulphide.
Write complete reaction for the bromination of phenol in aqueous and non-aqueous medium.
Draw structure of the following compound.
Prop-2-en-1-ol
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
