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प्रश्न
3-Methylbutane-2-ol on heating with HI gives ______
पर्याय
2-iodo-3-methylbutane
2-iodo-2-methylbutane
1-iodo-3-methylbutane
1-iodo-2-methylbutane
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उत्तर
2-iodo-2-methylbutane
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संबंधित प्रश्न
Write the IUPAC name of the following compound:

Write the IUPAC name of the following compound:
C6H5 – O – C2H5
Write structures of the compounds whose IUPAC names are as follows:
3-Chloromethylpentan-1-ol.
Give the IUPAC name of the following ether:
\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.........}|\\
\phantom{.............}\ce{CH3}
\end{array}\]
How is phenol converted into the following?
benzoquinone
Give reasons Fluoride ion has higher hydration enthalpy than chloride ion.
Write the IUPAC name of the following compound:

Write the structures of the products when Butan-2-ol reacts with CrO3
Write structural formulae for Cyclohex-2-en-1-ol.
Write IUPAC name of the following

Give IUPAC names of the following compound:

One of the following is not a dihydroxy derivative of benzene.
HBr reacts fastest with ____________.
n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent?
The major product formed by the reaction:
\[\begin{array}{cc}
\ce{CH3CH-CH2Br ->[CH3O^-][CH3OH] is}\\
|\phantom{................}\\
\ce{CH3}\phantom{.............}
\end{array}\]
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
Which of the following gives a positive iodoform test?
\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]
The product ‘Z’ is:
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.
Arrange the following compounds in decreasing order of acidity.
\[\ce{H2O, ROH, HC ≡ CH}\]
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 |
Assertion: IUPAC name of the compound
\[\begin{array}{cc}
\ce{CH3 - CH - O - CH2 - CH2 - CH3}\\
|\phantom{....................}\\
\ce{CH3}\phantom{.................}
\end{array}\] is 2-Ethoxy-2-methylethane.
Reason: In IUPAC nomenclature, ether is regarded as hydrocarbon derivative in which a hydrogen atom is replaced by —OR or —OAr group [where R = alkyl group and Ar = aryl group]
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.
How can phenol be converted to aspirin?
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.
Write the IUPAC name.
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]
Write IUPAC names of the following compounds:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3\phantom{...}OH\phantom{...}CH3}\\
\end{array}\]






