CUET-UG SERIES
Chemistry

Ethers

6 previous year questions.

Volume: 6 Ques
Yield: Medium

High-Yield Trend

3
2025
3
2023

Chapter Questions
6 MCQs

01
PYQ 2023
medium
chemistry ID: cuet-ug-
Glycoside linkage is the ether bond present in between two:
1
Amino acids
2
Nucleic acids
3
Vitamins
4
Monosaccharides
02
PYQ 2023
medium
chemistry ID: cuet-ug-
Among the following ethers, which cannot react with HI?
1
ethers, which cannot react with HI?
2
ethers, which cannot react with HI?
3
ethers, which cannot react with HI?
4
ethers, which cannot react with HI?
03
PYQ 2023
medium
chemistry ID: cuet-ug-
What would be the expected product when dimethyl ether is treated with HI in excess
1
Methyl alcohol and Methyl iodide
2
Methyl iodide only
3
Ethyl alcohol only
4
Ethene only
04
PYQ 2025
hard
chemistry ID: cuet-ug-
What happens when C₆H₅–O–R is treated with HX?
1
RX and C₆H₅OH are formed
2
ROH and C₆H₅X are formed
3
C₆H₄X₂ and ROH are formed
4
RX and C₆H₅X are formed
05
PYQ 2025
medium
chemistry ID: cuet-ug-
Which of the following reagents is required for the conversion of Benzene to methyl benzoate?
(A) Br /FeBr
(B) Mg, dry Ether
(C) CO , H O
(D) Methanol, Conc. H SO
1
(A), (B) and (C) only
2
(A), (B) and (D) only
3
(A), (B), (C) and (D)
4
(B), (C) and (D) only
06
PYQ 2025
easy
chemistry ID: cuet-ug-

Replacement of a hydrogen atom in a hydrocarbon by an alkoxy or carboxyl group yields a class of compounds known as ethers. Ethers are classified as symmetrical or unsymmetrical on the basis of groups attached to the oxygen atoms. Diethyl ether, a symmetrical ether, has been widely used as an inhalation anesthetic. Ethers can be prepared by acid catalyzed intermolecular dehydration of alcohols and Williamson's synthesis. Acid catalyzed dehydration of alcohols is not generally preferred as it gives a mixture of elimination and substitution products. In Williamson's synthesis, an alkyl halide is allowed to react with sodium alkoxide. Ethers containing substituted Alkyl groups may also be prepared by this method. The C-O bond in ether is weakly polar and is cleaved under drastic conditions with excess of hydrogen halides. In electrophilic substitution, the alkoxy group deactivates the aromatic ring and directs the incoming group to ortho and para positions.