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प्रश्न
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 |
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उत्तर
| Column I | Column II | |
| (i) | ![]() |
(d) o-Cresol |
| (ii) | ![]() |
(c) Catechol |
| (iii) | ![]() |
(f) Resorcinol |
| (iv) | ![]() |
(a) Hydroquinone |
| (v) | ![]() |
(g) Anisole |
| (vi) | ![]() |
(b) Phenetole |
Explanation:
(i) Cresols are organic compounds which are methyl phenols. There are three forms of cresol: o-cresol, p-cresol and m-cresol.
(ii) Catechol is also known as pyrocatechol. Its IUPAC name is 1, 2-dihydrobenzene. It is used in the production of pesticides, perfumes and pharmaceuticals.
(iii) Its IUPAC name is 1, 3-dihydroxybenzene. Resorcinol is used to treat acne, seborrheic dermatitis and other skin disorder.
(iv) Hydroquinone is also known as quinol. Its IUPAC name is 1, 4-dihydroxybenzene. It is a white granular solid. It is a good reducing agent.
(v) Anisole or methoxy benzene, is a colourless liquid with a smell reminiscent of an anise seed.
(vi) Phenetole is an organic compound. It is also known as ethyl phenyl ether. It is volatile in nature and its vapour is explosive in nature.
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संबंधित प्रश्न
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:
\[\begin{array}{cc}
\phantom{........................}\ce{CH3}\\
\phantom{....................}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.........}|\phantom{.........}|\\
\phantom{...}\ce{CH3}\phantom{....}\ce{OH}\phantom{....}\ce{CH3}\\
\end{array}\]
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
|\phantom{....................}|\phantom{.........}|\phantom{.............}\\
\ce{OH}\phantom{................}\ce{OH}\phantom{...}\ce{C{_2}H5}\phantom{.........}\\
\end{array}\]
Give the IUPAC name of the following ether:
\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.........}|\\
\phantom{.............}\ce{CH3}
\end{array}\]
Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.
(A) formaldehyde
(B) acetaldehyde
(C) acetone
(D) ethyl methyl ketone
Write the structure and IUPAC name of 'methyl-n-propyl ether'.
3-Methylbutane-2-ol on heating with HI gives ______
How is phenol converted into the following?
picric acid
Write the structures of the products when Butan-2-ol reacts with CrO3
Propanoic acid to ethylamine.
Write structural formulae for 3-Methoxyhexane
Write IUPAC names of the following

C6H5OCH2CH3 is called:
Butane-2-ol is ____________.
The heating of phenyl methyl ether with HI produces:
The correct acidic strength order of the following is:

(I)

(II)

(III)
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.
Identify A and B in the following:

Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.






