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प्रश्न
Explain metamerism with suitable examples of ethers
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उत्तर
The property in which ethers have same molecular formula but different alkyl groups in their structures is called metamerism and the isomers obtained are called as metamers.
Examples :
e.g. C2H5 - O - C2H5 - Diethyl ether;
CH3 - O - C3H7 - Methyl n-propyl ether
In the above example both ethers are having same molecular formula i.e. C4H10 but different alkyl groups in their structure, so they are metamers of each other.
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संबंधित प्रश्न
Write the IUPAC name of the given compound:

Name the following compound according to IUPAC system.

Name the following compound according to IUPAC system.
\[\begin{array}{cc}
\ce{H2C = CH - CH - CH2 - CH2 - CH3}\\
|\phantom{..........}\\
\ce{OH}\phantom{........}
\end{array}\]
Name the following compound according to IUPAC system.
\[\begin{array}{cc}
\ce{CH3 - C = C - CH2OH}\\
\phantom{}|\phantom{....}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{.}\ce{Br}\phantom{...}
\end{array}\]
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:

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:
C6H5 – O – C7H15(n−)
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:
\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{CH3}
\end{array}\]
Give IUPAC name of the following ether:

Give 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
What is the action of hot HI on it?
3-Methylbutane-2-ol on heating with HI gives ______
How is phenol converted into the following?
Benzene
How is phenol converted into the following?
benzoquinone
How is phenol converted into the following?
picric acid
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
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 formula for Methyl vinyl ether.
Write structural formula for pentane-1,4-diol.
Write structural formulae for Cyclohex-2-en-1-ol.
Write IUPAC names of the following

Glycerol is ____________.
3-methylphenol is called ____________.
One of the following is not a dihydroxy derivative of benzene.
An example of a compound with functional group – O – is ____________.
Butane-2-ol is ____________.
Cresol has ____________.
n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent?
Ethylene reacts with Baeyer’s reagent to give ______.
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 heating of phenyl methyl ether with HI produces:
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:
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)
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: 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: Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.
Reason: Lewis acid polarises the bromine molecule.
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 complete reaction for the bromination of phenol in aqueous and non-aqueous medium.
Explain why Lewis acid is not required in bromination of phenol?
How can phenol be converted to aspirin?
Draw structure of the following compound.
2. 5-Diethylphenol
Draw structure of the following compound.
2-Methoxypropane
Write structural formulae for:
p-Nitrophenol
Write structural formulae for:
Salicylic acid
The IUPAC name of
is ______.
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{..............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.....}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{.}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
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 names of the following compounds:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3\phantom{...}OH\phantom{...}CH3}\\
\end{array}\]
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
