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प्रश्न
What is the action of hot HI on it?
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उत्तर
Action of hot HI on methyl n-propyl ether:
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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:
C6H5 – O – C7H15(n−)
Give the IUPAC name of the following ether:
CH3OCH2CH2Cl
Give the IUPAC name of the following ether:
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
Write the structure and IUPAC name of 'methyl-n-propyl ether'.
3-Methylbutane-2-ol on heating with HI gives ______
Write the IUPAC name of the following compound:
Write the structures of the products when Butan-2-ol reacts with CrO3
What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?
Write structural formulae for 3-Methoxyhexane
Write a structural formula for methyl vinyl ether.
Write IUPAC name of the following
Write IUPAC names of the following
C6H5OCH2CH3 is called:
An example of a compound with functional group – O – is ____________.
The IUPAC name of the ether CH2 = CH–CH2OCH3 is:
The major product formed by the reaction:
\[\begin{array}{cc}
\ce{CH3CH-CH2Br ->[CH3O^-][CH3OH] is}\\
|\phantom{................}\\
\ce{CH3}\phantom{.............}
\end{array}\]
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]
The product ‘Z’ is:
Which of the following compounds will react with sodium hydroxide solution in water?
Explain why p-nitrophenol is more acidic than phenol.
Assertion: Addition reaction of water to but-1-ene in acidic medium yields butan-1-ol.
Reason: Addition of water in acidic medium proceeds through the formation of primary carbocation.
Assertion: Phenol forms 2, 4, 6 – tribromophenol on treatment with \[\ce{Br2}\] in carbon disulphide at 273 K.
Reason: Bromine polarises in carbon disulphide.
Assertion: Phenols give o- and p-nitrophenol on nitration with conc. \[\ce{HNO3}\] and \[\ce{H2SO4}\] mixture.
Reason: –OH group in phenol is o–, p– directing.
Write a chemical reaction for the following conversion:
Acetic acid into ethyl alcohol.
How are the following conversions carried out?
Methyl magnesium bromide→2-Methylpropan-2-ol.
Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.
