NEET-UG and JEE Main Chemistry · Class 12
Ethers - preparation and properties — NEET & JEE Questions
Ethers - preparation and properties is a topic in Organic Compounds Containing Oxygen, a Class 12 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 15 published NEET-UG and JEE Main questions on Ethers - preparation and properties, each with the marking scheme of the real paper.
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Ethers - preparation and properties MCQs with solutions
10 of the 15 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.
The Williamson ether synthesis prepares ethers by reacting an alkoxide ion with typically a
- A. primary alkyl halide
- B. carboxylic acid only
- C. ketone only
- D. tertiary carbocation in water
Given below are two statements : Statement I : Dimethyl ether is completely soluble in water. However, diethyl ether is soluble in water to a very small extent. Statement II : Sodium metal can be used to dry diethyl ether and not ethyl alcohol. In the light of given statements. choose the correct answer from the options given below
- A. Statement I is false but Statement II are true
- B. Statement I is true but Statement II is false
- C. Both Statement I and Statement II are true
- D. Both Statement I and Statement II are False
Suitable reaction condition for preparation of Methyl phenyl ether is
- A. Benzene, MeBr
- B. , MeBr
- C. Ph - Br,
- D. , MeOH
Ethers generally have lower boiling points than isomeric alcohols mainly because ethers
- A. cannot form intermolecular O-H hydrogen bonds with one another
- B. contain no oxygen
- C. are ionic compounds
- D. have much larger molecular masses in every case
0.1 mole of compound âSâ will weigh ___________ g. (Given molar mass in g mol â1 C : 12, H : 1, O : 16)
Statement I : In the above reaction, product formed will be a mixture of benzyl alcohol and iodobenzene. Statement II : In the above reaction, the bond is cleaved to give the product. In the light of the above statements, choose the correct answer from the options given below :
- A. Both Statement I and Statement II are true
- B. Both Statement I and Statement II are false
- C. Statement I is true but Statement II is false
- D. Statement I is false but Statement II is true
Given below are two statements : Statement I : Statement II : In , intramolecular substitution takes place first by involving lone pair of electrons on nitrogen. In the light of the above statements, choose the most appropriate answer from the options given below
- A. Both Statement I and Statement II are correct
- B. Statement I is incorrect but Statement II is correct
- C. Both Statement I and Statement II are incorrect
- D. Statement I is correct but Statement II is incorrect
For the Compounds : (A) (B) (C) (D) The increasing order of boiling point is : Choose the correct answer from the options given below :
- A.
- B.
- C.
- D.
2-Methyl propyl bromide reacts with and gives 'A' whereas on reaction with it gives 'B'. The mechanism followed in these reactions and the products 'A' and 'B' respectively are :
- A. tert-butyl ethyl ether; iso-butyl ethyl ether
- B. tert-butyl ethyl ether; 2-butyl ethyl ether
- C. iso-butyl ethyl ether; tert-butyl ethyl ether
- D. 2-butyl ethyl ether; iso-butyl ethyl ether
Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R). Assertion (A) : Synthesis of ethyl phenyl ether may be achieved by Williamson synthesis. Reason (R) : Reaction of bromobenzene with sodium ethoxide yields ethyl phenyl ether. In the light of the above statements, choose the most appropriate answer from the options given below :
- A. Both (A) and (R) are correct and (R) is the correct explanation of (A)
- B. (A) is correct but (R) is not correct
- C. (A) is not correct but (R) is correct
- D. Both (A) and (R) are correct but (R) is not the correct explanation of (A).
Common mistakes in Ethers - preparation and properties
Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.
- Predicts elimination or alcohol formation instead of nucleophilic substitution.
- Places the bulky tertiary group on the alkyl halide and expects efficient SN2 attack.
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