Total number of stereoisomers of the compound:-

1. 10

2. 8

3. 6

4. 4

Subtopic:  Stereo Isomers |
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The effect that makes 2,3–dimethyl-2-butene more stable than 2-butene is-

1. Resonance

2. Hyperconjugation

3. Steric effect

4. Inductive effect

Subtopic:  Electron Displacement Effects |
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The IUPAC name of the above mentioned compound is - 

1. Cyclohexylidenemethanone

2. Cyclohexylidemethanone

3. Cyclohexylidenylmethanone

4. Cyclohexdenemethanone

Subtopic:  Nomenclature |
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Paper chromatography is an example of:

1. Partition chromatography

2. Thin layer chromatography

3. Column chromatography

4. Adsorption chromatography

Subtopic:  Purification of Organic Compounds |
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Which among these can exhibit tautomerism?

1. a only

2. b only

3. c only

4. a and c

Subtopic:  Structural Isomers |
 56%
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A tertiary butyl carbocation is more stable than a secondary butyl carbocation because-

1. + R effect of CH3 groups 

2. -R effect of - CH3  groups 

3. Hyperconjugation 

4. -l effect of -CH3 groups 

Subtopic:  Electron Displacement Effects | Reaction Intermediates ; Preparation & Properties |
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The IUPAC name of the compound is :

1. 2,3 - Diemethylheptane

2. 3- Methyl -4- ethyloctane

3. 5-Ethyl -6-methyloctane

4. 4-Ethyl -3 - methyloctane.

Subtopic:  Nomenclature |
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The pair of structures that does not represent isomers is:

1. 2.
3. 4.

Subtopic:  Structural Isomers |
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The presence of a halogen on the benzene ring in a nitration reaction leads to:

1. Direct nitro group to come at meta and deactivate the ring due to –I effect of halogen.
2. Direct nitro group to come at ortho and para position and deactivate the ring due to –I effect of halogen.
3. Direct nitro group to come at meta and activate the ring toward nitration reaction.
4. Nitration reaction does not take place due to deactivation caused by –I effect of halogen.
Subtopic:  Types of Reaction |
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The most stable carbocation among the following is-

1. 2.
3. 4.

Subtopic:  Reaction Intermediates ; Preparation & Properties |
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