हिंदी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

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) - Chemistry

Advertisements
Advertisements

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
जोड़ियाँ मिलाइएँ
Advertisements

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.

shaalaa.com
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 11: Alcohols, Phenols and Ethers - Multiple Choice Questions (Type - I) [पृष्ठ १६०]

APPEARS IN

एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
अध्याय 11 Alcohols, Phenols and Ethers
Multiple Choice Questions (Type - I) | Q 57 | पृष्ठ १६०

संबंधित प्रश्न

Write IUPAC name of the following compound:

C6H5 – O – C7H15(n−)


Write IUPAC name of the following compound:

\[\begin{array}{cc}
\ce{CH3 - CH2 - O - CH - CH2 - CH3}\\
\phantom{...}|\\
\phantom{.....}\ce{CH3}
\end{array}\]


Give IUPAC name of the following ether:


Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.

(A) formaldehyde

(B) acetaldehyde

(C) acetone

(D) ethyl methyl ketone


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


3-Methylbutane-2-ol on heating with HI gives ______


Write IUPAC name of the following compound (CH3)2 N − CH2CH3


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


Propanoic acid to ethylamine.


Write structural formulae for 1-Ethylcyclohexanol.


Write IUPAC names of the following


Write IUPAC names of the following


C6H5OCH2CH3 is called:


Ethylene reacts with Baeyer’s reagent to give ______.


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.


Draw structure of the following compound.

Prop-2-en-1-ol


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.

\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C  -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×