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Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025 PDF Download

Q.1. Considering the basic strength of amines in aqueous solution, which one has

the smallest pKb value?

(1) (CH3)3N

(2) C6H5NH2

(3) (CH3)2NH

(4) CH3NH2

Correct answer is option (3).

  • Because of resonance, aryalamines are less basic than alkyl amines. 
  • In aryalamines, the lone pair of electrons on N is partly shared with the ring and is less available for sharing with a proton. 
  • In alkylamines, the electron releasing alkyl group increases the electron density on nitrogen atom. Hence increases the protonation ability of amines. So, more the number of alkyl groups, higher will be basicity of amine. 
  • Because of steric effect, a slight discrepancy occurs in case of trimethyl amine. So (CH3)2NH has the smallest pKb value.
  • Hence option (3) is the answer.


Q.2 The compound formed in the positive test for nitrogen with the Lassaigne solution of an organic compound is

(1) Fe4[Fe(CN)6]3

(2) Na4[Fe(CN)5NOS]

(3) Fe(CN)3

(4) Na3[Fe(CN)6]

Correct option is Option (1)
The compound formed in the positive test for nitrogen with the Lassaigne solution of an organic compound is prussian blue coloured complex compound ferric ferrocyanide.

Hence option (1) is the answer.

Q.3. Arrange the following compounds in order of decreasing acidity:  (IIT- JEE 2013)
Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025(1) I  > II > III > IV
(2) III > I > II > IV
(3) IV > III > I > II
(4) II > IV > I > III

Correct Answer is Option (2)

  • Electron donating groups increase the acidity of phenol when present as a substituent on the benzene ring while electron-withdrawing groups decrease the acidity of phenol.
  • Cl and NO2 are electron-withdrawing groups while -CH3 and -OCH3 are electron donating groups.
  • However, nitro undergoes resonance, which allows it to better stabilize the negative charge of the oxygen compared to chlorine. Thus, acidic character of nitrophenol would be higher than that of chlorophenol.
  • So, Nitrophenol is the most acidic compound here followed by chlorophenol.
    Hence, the correct option is 2.

Q.4. Which of the given statement(s) about N, O, P and Q with respect to M is (are) correct?    (IIT-JEE 2012)
Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025(1) M and N are non–mirror image stereoisomers.
(2) M and O are identical.
(3) M and P are enantiomers.
(4) M and Q are identical.

Correct Answer is Option (1), (2) & (3)
Fischer Projections of the molecules:
Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025
It is clear that:

  • M and N are non-mirror image stereoisomers.
  • M and O are the same molecules i.e. Identical.
  • M and P are the non-superimposable mirror images of hence they are enantiomers.
  • N and Q are identical.
  • M and Q are also are non–mirror image stereoisomers i.e diastereomers.
    Hence 1, 2 and 3 are the correct statements.

Q.5. Among the following oxoacids, the correct decreasing order of acid strength is :

(1) HClO4 > HClO3 > HClO2 > HOCl

(2) HClO2 > HClO4 > HClO3 > HOCl

(3) HOCl > HClO2 > HClO3 > HClO4

(4) HClO4 > HOCl > HClO2 > HClO3

Correct option is Option (1)

Acidic strength is directly proportional to the oxidation number. Increasing acid strength is because of an increase in the oxidation state of the central atom.

Hence option (1) is the answer.

Q.6. The correct order of increasing basicity of the given conjugate base (R =CH3) is:

(1) RCOO < HC ≡ C < NH2 < R

(2) RCOO < HC ≡ C < R– < NH2

(3) R < HC ≡ C < RCOO < NH2

(4) RCOO < NH2 < HC ≡ C– < R

Correct option is Option (1)

  • The basic strength is inversely proportional to the stability of conjugate base.
  •  In basicity, if the availability of the electrons is more, then more readily they can be donated to form a new bond to the proton and, and hence the stronger base. 
  • If bronsted acid is a strong acid then its conjugate base is a weak base .
  • The correct order of increasing basic strength is RCOO < HC ≡ C < NH2 < R
  • Hence option (1) is the answer.


Q.7. In gaseous triethyl amine the "CNC" bond angle is _________ degree. (JEE 2021)

Solution: In gaseous triethyl amine the "CNC" bond angle is 108 degree.  


Q.8. Consider the below chemical reaction. The total number of stereoisomers possible for Product 'P' is _____________.                                      (JEE 2021)

Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025

Solution: The total number of products possible = 2 
Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025

Q.9. Which one the following does not have sp2 hybridized carbon?

(1) Acetone

(2) Acetamide

(3) Acetonitrile

(4) Acetic acid

Correct option is Option (3)

Acetonitrile is having only sp3 and sp hybridized carbon atoms.

Hence option (3) is the answer.

Q.10. The total number of cyclic isomers possible for a hydrocarbon with the molecular formula C4H6 is ____   (IIT-JEE 2010)

5 cyclic isomers are possible for C4H6, possible.
Solved Examples for JEE: General Organic Chemistry | Mock Tests for JEE Main and Advanced 2025

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FAQs on Solved Examples for JEE: General Organic Chemistry - Mock Tests for JEE Main and Advanced 2025

1. What are the important topics to study in General Organic Chemistry for JEE?
Ans. Some of the important topics to study in General Organic Chemistry for JEE are - Isomerism, Nomenclature, Stereochemistry, Reaction Mechanism, Aromaticity, and Organic Synthesis.
2. What is the difference between SN1 and SN2 reactions?
Ans. SN1 and SN2 are two types of nucleophilic substitution reactions. SN1 reactions are unimolecular, meaning the rate-determining step involves only one molecule. SN2 reactions are bimolecular, meaning the rate-determining step involves two molecules. SN1 reactions occur in two steps, while SN2 reactions occur in one step. SN1 reactions result in racemic mixture, while SN2 reactions result in a stereospecific product.
3. What are enantiomers?
Ans. Enantiomers are a type of stereoisomers that are non-superimposable mirror images of each other. They have the same physical and chemical properties but differ in their optical activity. Enantiomers rotate the plane of polarized light in opposite directions.
4. What is the difference between a primary, secondary, and tertiary alcohol?
Ans. Primary, secondary, and tertiary alcohols are classified based on the number of carbon atoms bonded to the carbon atom bearing the hydroxyl group. Primary alcohols have one carbon atom bonded to the carbon atom bearing the hydroxyl group, secondary alcohols have two, and tertiary alcohols have three. This classification is important as it affects the reactivity of alcohols in various chemical reactions.
5. What is the role of catalysts in organic reactions?
Ans. Catalysts increase the rate of chemical reactions without being consumed in the reaction themselves. In organic reactions, catalysts can be used to increase the yield of desired products, reduce unwanted side reactions, and improve reaction selectivity. Catalysts can be either homogeneous or heterogeneous, and they can function by providing an alternative reaction pathway with lower activation energy or by stabilizing the transition state of the reaction.
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