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Carbonyl Group MCQ - 1 (Advanced) - JEE MCQ


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25 Questions MCQ Test - Carbonyl Group MCQ - 1 (Advanced)

Carbonyl Group MCQ - 1 (Advanced) for JEE 2024 is part of JEE preparation. The Carbonyl Group MCQ - 1 (Advanced) questions and answers have been prepared according to the JEE exam syllabus.The Carbonyl Group MCQ - 1 (Advanced) MCQs are made for JEE 2024 Exam. Find important definitions, questions, notes, meanings, examples, exercises, MCQs and online tests for Carbonyl Group MCQ - 1 (Advanced) below.
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Carbonyl Group MCQ - 1 (Advanced) - Question 1

Nucleophilic substitution at acyl carbon of a carboxylic acid derivative generally proceeds by.

Carbonyl Group MCQ - 1 (Advanced) - Question 2

The correct order of decreasing reactivity of the given compound towards hydrolysis under identical condition is:

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Carbonyl Group MCQ - 1 (Advanced) - Question 3

Which of the following proposed reactions would take place most quickly under mild conditions ?

Carbonyl Group MCQ - 1 (Advanced) - Question 4

In the given reaction sequene :

C6H5_CN  A  B C, (C) is

Carbonyl Group MCQ - 1 (Advanced) - Question 5

H2N–NH2+Ph – –Cl (excess)  X, X is

Carbonyl Group MCQ - 1 (Advanced) - Question 6

 Phosgene(COCl2) + 1 mol C2H5OH  X, X is

Carbonyl Group MCQ - 1 (Advanced) - Question 7

What is the IUPAC name of the sown compound?

Detailed Solution for Carbonyl Group MCQ - 1 (Advanced) - Question 7

Explanation: There are three aldehydic groups present in the given compound and none of them have preference over the other. The CHO groups are considered as substituents with the parent chain containing only three carbon atoms. This is done to give identical treatment to all the aldehydic groups.

Carbonyl Group MCQ - 1 (Advanced) - Question 8

  + CH3CH2CH2CH2 NH2  X, X is

Detailed Solution for Carbonyl Group MCQ - 1 (Advanced) - Question 8
The lone pairs of nitrogen will attack at the nucleophilic carbonyl carbon.. 1 mole HCĺ will get eliminated.
again the lone pair of N will attack like previous one and another mole HCl will get eliminated.
in this whole method the carbon chain attached to nitrogen atom will stay unaffected.
hence option c is correct.
Carbonyl Group MCQ - 1 (Advanced) - Question 9

  +  X, X is

Carbonyl Group MCQ - 1 (Advanced) - Question 10

(CH3)3C––Cl+LiAlH4 (excess)   X, X is

Carbonyl Group MCQ - 1 (Advanced) - Question 11

For the given reaction

Carbonyl Group MCQ - 1 (Advanced) - Question 12

 PhCH2 – –Cl + CH3CH2SH ® X, X is

Carbonyl Group MCQ - 1 (Advanced) - Question 13

 List the following esters in order of decreasing reactivity in the second step of a nucleophilic acyl substitution reaction.

(I)  (II) 

(III)  (IV) 

Select the correct answer from the codes given below:

Carbonyl Group MCQ - 1 (Advanced) - Question 14

Which one of the following is least reactive for hydrolysis reaction ?

Carbonyl Group MCQ - 1 (Advanced) - Question 15

Which one of the following esters is most reactive for saponification ?

Carbonyl Group MCQ - 1 (Advanced) - Question 16

 Consider the following statements for hydrolysis reaction :

(I)  is more reactive than C6H5COOC2H5

(II)  is more reactive than 

(III)  is more reactive than 

Of these the correct statements are

Carbonyl Group MCQ - 1 (Advanced) - Question 17

 Ease of esterification of following acids with CH3OH

(I) HCOOH (II) CH3 COOH (III) CH3 – CH2 – COOH (IV) CH3 – – COOH, is

Carbonyl Group MCQ - 1 (Advanced) - Question 18

 The oxidation of primary alcohols give

Carbonyl Group MCQ - 1 (Advanced) - Question 19

 In the given reaction

  [P], [P] will be :

Carbonyl Group MCQ - 1 (Advanced) - Question 20

In the given reaction

 [X], [X] is

Carbonyl Group MCQ - 1 (Advanced) - Question 21

In the given reaction

C2H5–O––O–C2H5+HO–CH 2–CH2–OH  [X], [X] is

Carbonyl Group MCQ - 1 (Advanced) - Question 22

  X, X is

Carbonyl Group MCQ - 1 (Advanced) - Question 23

 

Carbonyl Group MCQ - 1 (Advanced) - Question 24

 Ease of esterification of following alcohol with HCOOH is

(I) CH3–CH2OH (II) (CH3)2CH–OH (III) (CH3)3C–OH

Carbonyl Group MCQ - 1 (Advanced) - Question 25

The product x in the above reaction is

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