The most stable carbocation among the following is:

1. 2.
3. 4.

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 78%
Level 2: 60%+
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The arrangement in decreasing order of stability of CH3C2H5,(CH3)2CH and (CH3)3 C free radicals is-

1. CH3C2H5 > (CH3)2CH > (CH3)3 C  

2. (CH3)3 C > (CH3)2CH > C2H5CH3

3. C2H5CH3 > (CH3)2CH > (CH3)3 C

4. (CH3)3 C > (CH3)2CH >  CH3  > C2H5 

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 86%
Level 1: 80%+
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The species that contains only three pairs of electrons among the following is-

1. Carbocation 2. Carbanion
3. Free radical 4. None of the above
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 64%
Level 2: 60%+
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Arrange H, CH₃, C₂H₅, and C₃H₇ in order of increasing positive inductive effect:

1. H < CH3 < C2H5 < C3H7

2. H> CH3 <C2H5 > C3H7

3. H < C2H5 < CH3 <C3H7

4. None of the above

Subtopic:  Electron Displacement Effects |
 83%
Level 1: 80%+
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Which of the following statements accurately describes the stability of allyl and propyl carbocations?

1. Allyl carbocation (CH2=CH-CH2+) is more stable than propyl carbocation.

2. Propyl carbocation is more stable than allyl carbocation.

3. Both are equally stable.

4. None of the above.

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 70%
Level 2: 60%+
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What is the relationship between the two given molecular structures?

1. Enantiomers 2. Position isomers
3. Conformers 4. None of the above
Subtopic:  Conformational Isomers |
 66%
Level 2: 60%+
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Geometrical isomerism is caused by-

1. Restricted rotation around C=C bond.

2. The presence of one asymmetric carbon atom.

3. The different groups attached to the same functional group.

4. None of the above.

Subtopic:  Stereo Isomers |
 87%
Level 1: 80%+
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A total number of structural isomeric aldehydes and ketones that can exist with
the molecular formula C5H10O are :
1. 5
2. 8
3. 6
4. 7
 

Subtopic:  Stereo Isomers |
Level 3: 35%-60%
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 Alkyl cyanide \(R-C \equiv N\) and alkyl isocyanides \(R- \overset{+}{N} \equiv C^-\) are: 

1. Tautomers 2. Metamers
3. Functional isomers 4.  Geometrical isomers
Subtopic:  Structural Isomers |
 79%
Level 2: 60%+
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The optically active compound among the following is-

1. Glycerine 2. Acetaldehyde
3. Glyceraldehyde 4. Acetone
Subtopic:  Stereo Isomers |
 61%
Level 2: 60%+
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