Preparation & Reaction of Phenols - Free MCQ Practice Test with solutions,
MCQ Practice Test & Solutions: Test: Preparation & Reaction of Phenols (15 Questions)
You can prepare effectively for JEE Chemistry for JEE Main & Advanced with this dedicated MCQ Practice Test (available with solutions) on the important topic of "Test: Preparation & Reaction of Phenols". These 15 questions have been designed by the experts with the latest curriculum of JEE 2026, to help you master the concept.
Test Highlights:
- - Format: Multiple Choice Questions (MCQ)
- - Duration: 20 minutes
- - Number of Questions: 15
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On heating aqueous solution of benzene diazonium chloride, which of the following is formed?
Detailed Solution: Question 1
For the reaction
The correct statement regarding above reaction is
The correct statement regarding above reaction is
Detailed Solution: Question 2
The conversion of O-acylated phenol in presence of 
to 
-acylated phenol is an example for this type of organic reaction
to -acylated phenol is an example for this type of organic reactionDetailed Solution: Question 3
Identify the product in the following reaction.
Detailed Solution: Question 4
What amount of bromine will be required to convert 
of phenol into 
-tribromophenol?
of phenol into -tribromophenol?Detailed Solution: Question 5
of phenol require 
of phenol require 
An optically active alcohol of formula 
produced the following compound when refluxed with 
The original compound showed these properties also:
What is structure of 
?
produced the following compound when refluxed with The original compound showed these properties also:
What is structure of
?Detailed Solution: Question 6
Which of the following reactions will not result in the formation of anisole?
Detailed Solution: Question 7
to give 
, and not anisole
Which of the following compound can react with hydroxylamine?
Detailed Solution: Question 8
The products formed in the reaction of phenol with 
dissolved in 
at 
are
dissolved in at areDetailed Solution: Question 9
in the presence of non-polar solvent 
, it gives only o- and 
-bromophenols instead the trisubstituted products. Reason for the above observation is supression of phenoxide ion in non-polar solvent. Thus, we get only mono substituted products.
Identify the nature of product in the following reaction
Detailed Solution: Question 10
is an example of Elbs persulphate oxidation.Phenol can be distinguished from alcohol with
Detailed Solution: Question 11
Phenol gives violet colour with neutral 
Sodium phenoxide when heated with 
under pressure at 
yields a product which on acetylation produces 
The major product 
would be
under pressure at yields a product which on acetylation produces The major product
would beDetailed Solution: Question 12
Detailed Solution: Question 13
Which one of the following substituents at paraposition is most effective in stabilizing the phenoxide
ion?
ion?
Detailed Solution: Question 14
and 
are electron donating group and hence decrease the stability of benzene ring 
is weaker electron withdrawing group than 
. Hence 
group more stabilize the phenoxide ion at 
-position.1-Phenylethanol can be prepared by reaction of benzaldehyde with
Detailed Solution: Question 15
alcohol and can be prepared by the reaction of benzaldehyde with Grignard reagent 
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