Advertisements
Advertisements
प्रश्न
Give the IUPAC name of the following ether:
O2N – C6H4 – OCH3(p)
Advertisements
उत्तर
4-Nitroanisole
APPEARS IN
संबंधित प्रश्न
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:
C6H5 – O – C7H15(n−)
Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.
(A) formaldehyde
(B) acetaldehyde
(C) acetone
(D) ethyl methyl ketone
Natalite is a mixture of
(a) diethyl ether and methanol
(b) diethyl ether and ethanol
(c) dimethyl ether and methanol
(d) dimethyl ether and ethanol
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
Propanoic acid to ethylamine.
Resorcinol on distillation with zinc dust gives _________.
Write IUPAC name of the following
\[\begin{array}{cc}\ce{CH3-CH-CH-CH2-OH}\\|\phantom{.....}|\phantom{.......}\\\ce{OH}\phantom{..}\ce{CH3}\phantom{.....}\end{array}\]
Isopropyl alcohol on oxidation forms:
The product of acid catalysed hydration of 2-phenylpropene is:
The heating of phenyl methyl ether with HI produces:
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.
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.
Write complete reaction for the bromination of phenol in aqueous and non-aqueous medium.
The IUPAC name of 
is ______.
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
