Total number of substituents present in the following compound are:
1. 4 2. 5
3. 7 4. 3

Subtopic:  Nomenclature |
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IUPAC name of the following compound is:



1. 1, 2 - Dimethylcyclohexene
2. 2, 3 - Dimethylcyclohexene
3. 1, 2 - Dimethylcyclohex-2-ene
4. 1, 6 - Dimethylcyclohexene
Subtopic:  Nomenclature |
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A steam volatile organic compound which is immiscible with water has a boiling point of \(250^\circ \text{C}\). During steam distillation, a mixture of this organic compound and water will boil:

1. Above \(100^\circ \text{C}\) but below \(250^\circ \text{C}\).
2. Above \(250^\circ \text{C}\).
3. At \(250^\circ \text{C}\).    
4. Close to but below \(100^\circ \text{C}\).
Subtopic:  Qualitative Analysis of Organic Compounds |
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NEET - 2024
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NEET 2026 - Target Batch - Vital
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Which of the following is the strongest nucleophile?
1. \( \text{HC} \equiv \text{C}^- \) 2. \(\text{H}_2\text{C} = \text{CH}^- \)
3. \(\text{CH}_3- \text{CH}_2^- \) 4. \(\text{NH}_2^-\)
Subtopic:  Nucleophile & Electrophile |
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Two compounds I and II are eluted by column chromatography (adsorption of I > II).
Which one of the following is a correct statement? 

1. II moves slower and has higher \(R_f\) value than I 
2. II moves faster and has higher \(R_f\) value than I 
3. I moves faster and has higher \(R_f\) value than II 
4. I moves slower and has higher \(R_f\) Value than II
Subtopic:  Purification of Organic Compounds |
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The Incorrect statement(s) concerning the structures E, F, and G is :


1. E,F, and G are resonance structures 
2. E,F and G are tautomers
3. F and G are geometrical isomers 
4. F and G are diastereomers
Subtopic:  Conformational Isomers |
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How many geometrical isomers are possible for a compound with the molecular formula \(\mathrm{C_2BrClFI}\)?

1. 3
2. 4
3. 5 
4. 6
Subtopic:  Stereo Isomers |
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The following compound is named as :
   
1. 6-Mercaptocyclohex-4-ene-1,3-diol
2. 1-Mercaptocyclohex-2-ene-4,6-diol 
3. 1-Mercaptocyclohex-5-ene-2,4-diol
4. 4-Mercaptocyclohex-2-ene-1,5-diol
Subtopic:  Nomenclature |
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What is correct about the following structure?


1. Total stereoisomers =4
2. Number of chiral carbons =1 
3. Number of optical isomers =2 
4. Number of meso compounds= 2
Subtopic:  Stereo Isomers |
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The hyperconjugation effect is not observed in: 
 
(i) (ii)       
(iii) (iv)

1. (i) and (ii)
2. (i), (ii) and (iii)
3. (i) only 
4. (i), (ii) and (iv) 
Subtopic:  Electron Displacement Effects |
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