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प्रश्न
3-Methylbutane-2-ol on heating with HI gives ______
विकल्प
2-iodo-3-methylbutane
2-iodo-2-methylbutane
1-iodo-3-methylbutane
1-iodo-2-methylbutane
उत्तर
2-iodo-2-methylbutane
APPEARS IN
संबंधित प्रश्न
What is metamerism?
Explain metamerism with suitable examples of ethers
Write the IUPAC name of the given compound:
Name the following compound according to IUPAC system.
\[\begin{array}{cc}
\phantom{............}\ce{CH2OH}\\
\phantom{......}|\\
\ce{CH3 - CH2 - CH - CH - CH - CH3}\\
\phantom{......}|\phantom{............}|\phantom{.}\\
\phantom{........}\ce{CH2Cl}\phantom{......}\ce{CH3}\phantom{}
\end{array}\]
Name the following compound according to IUPAC system.
\[\begin{array}{cc}
\phantom{........................}\ce{CH2OH}\\
\phantom{..................}|\\
\ce{CH3 - CH - CH2 - CH - CH - CH3}\\
\phantom{}|\phantom{.............}|\phantom{........}\\
\phantom{..}\ce{CH3}\phantom{..........}\ce{OH}\phantom{........}
\end{array}\]
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
\phantom{}|\phantom{.............}|\phantom{......}|\phantom{.........}\\
\phantom{}\ce{OH}\phantom{..........}\ce{OH}\phantom{...}\ce{C2H5}\phantom{......}
\end{array}\]
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - CH - CH - CH3}\\
|\phantom{......}|\phantom{..}\\
\ce{OH}\phantom{...}\ce{OH}\phantom{}
\end{array}\]
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{HO - CH2 - CH - CH2 - OH}\\
|\phantom{..}\\
\ce{OH}
\end{array}\]
Write IUPAC name of the following compound:
Write IUPAC name of the following compound:
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - O - CH2 - CH - CH3}\\
\phantom{..........}|\\
\phantom{............}\ce{CH3}
\end{array}\]
Write IUPAC name of the following compound:
C6H5 – O – C2H5
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - CH2 - O - CH - CH2 - CH3}\\
\phantom{...}|\\
\phantom{.....}\ce{CH3}
\end{array}\]
Write structures of the compounds whose IUPAC names are as follows:
3-Chloromethylpentan-1-ol.
- Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names.
- Classify the isomers of alcohols in the above question as primary, secondary and tertiary alcohols.
Give IUPAC name of the following ether:
O2N – C6H4 – OCH3(p)
Give IUPAC name of the following ether:
Give IUPAC name of the following ether:
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
Write the structure and IUPAC name of 'methyl-n-propyl ether'.
What is the action of hot HI on it?
How is phenol converted into the following?
benzene
Write IUPAC name of the following compound (CH3)2 N − CH2CH3
Give reasons Fluoride ion has higher hydration enthalpy than chloride ion.
Write the structures of the products when Butan-2-ol reacts with SOCl2
Write the IUPAC name of the following :
How do you convert the Ethanal to Propanone
In the dehydration of alcohols to alkenes by heating with concentrated sulphuric acid, the initiation step is:
(1) formation of carbonation
(2) formation of an ester
(3) protonation of the alcohol molecule
(4) elimination of water
What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?
Propanoic acid to ethylamine.
Write structural formulae for 1-Ethylcyclohexanol.
Write structural formulae for Pentane-1,4-diol
Write structural formulae for Cyclohex-2-en-1-ol.
Write IUPAC name of the following
\[\begin{array}{cc}\ce{CH3-CH-CH-CH2-OH}\\|\phantom{.....}|\phantom{.......}\\\ce{OH}\phantom{..}\ce{CH3}\phantom{.....}\end{array}\]
Write IUPAC names of the following
In a carbinol system of nomenclature tert.butyl alcohol is named as _______________
Isopropyl alcohol on oxidation forms:
Give IUPAC names of the following compound:
Give IUPAC names of the following compound:
\[\begin{array}{cc}
\phantom{..}\ce{H}\phantom{...}\ce{CH3}\phantom{.}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\ce{H - C - C - C - H}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\phantom{.}\ce{H}\phantom{...}\ce{OH}\phantom{.}\ce{H}\phantom{.}\\
\end{array}\]
C6H5OCH2CH3 is called:
One of the following is not a dihydroxy derivative of benzene.
Butane-2-ol is ____________.
Cresol has ____________.
IUPAC name of m-cresol is ____________.
Ethylene reacts with Baeyer’s reagent to give ______.
1-Propanol and 2-propanol can be best distinguished by:
Which of the following is most acidic?
The IUPAC name of the ether CH2 = CH–CH2OCH3 is:
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
The product of acid catalysed hydration of 2-phenylpropene is:
The heating of phenyl methyl ether with HI produces:
Which of the following gives a positive iodoform test?
Among the following sets of reactants which one produces anisole?
IUPAC name of the compound is:
\[\begin{array}{cc}
\ce{CH3-CH-OCH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]
The correct acidic strength order of the following is:
(I)
(II)
(III)
IUPAC name of m-cresol is ______.
IUPAC name of the compound \[\begin{array}{cc}
\ce{CH3 - CH - OCH3}\\
\phantom{}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{..}
\end{array}\] is ______.
Give IUPAC name of the compound given below.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH - CH2 - CH2 - CH - CH3}\phantom{.}\\
\phantom{.........}|\phantom{...................}|\phantom{...........}\\
\phantom{..}\ce{Cl}\phantom{.................}\ce{OH}\phantom{..}
\end{array}\]
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.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH2 - C = C - OH}\\
\phantom{........}|\phantom{....}|\phantom{}\\
\phantom{..............}\ce{CH3 CH2OH}
\end{array}\]
What happens when benzene diazonium chloride is heated with water?
Arrange the following compounds in decreasing order of acidity.
\[\ce{H2O, ROH, HC ≡ CH}\]
Explain why p-nitrophenol is more acidic than phenol.
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.
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]
Explain why Lewis acid is not required in bromination of phenol?
Write the IUPAC name of the following compound.
Convert the following:
Ethyl alcohol into ethyl acetate
Draw structure of the following compound.
2-Methoxypropane
Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.
Write structural formulae for:
p-Nitrophenol
Write structural formulae for:
Salicylic acid
The IUPAC name of 
is ______.
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
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 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 IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
