Consider the following species:
     
What is the hybridization of the carbon carrying a negative charge in structures (I) and (II), respectively?
1. sp2 and sp2 2. sp2 and sp3
3. sp and sp2 4. sp3 and sp3
Subtopic:  Hybridisation & Structure of Carbon Compounds |
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Total number of substituents present in the following compound are:
1. 4 2. 5
3. 7 4. 3
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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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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Indicate whether each of the following pairs are identical, or enantiomers and diastereomers ?

 

I

II

III

1.

enantiomers

diastereomers

enantiomers

2.

identical

enantiomers

enantiomers

3.

enantiomers

diastereomers

identical

4.

enantiomers

identical

identical

 

Subtopic:  Stereo Isomers |
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The correct order of nucleophilicity among the following is:

(I) CH3COO-

(II) CH3CO-

(III) CN-

(IV) 

1. I > II > III > IV

2. IV > III > II > I

3. II > III > I > IV

4. III > II > I > IV

Subtopic:  Nucleophile & Electrophile |
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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 |
From NCERT
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Consider the resonance structure of CH3COOCHas follows:



The correct statement among the following is-

1. I and II cannot be the major contributors to the real structure of CH3COOCH3
2. I and II can be the major contributors to the real structure of CH3COOCH3
3. I is more stable than II.
4. None of the above
Subtopic:  Electron Displacement Effects |
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In the above compound, at which bond proton H+ attack fastest?

1. A

2. B

3. C

4. D

Subtopic:  Acidic & Basic Character |
From NCERT
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What is the correct order of stability for the following carbanions?
1.  2. 
3.  4. 
      

1.  (1) > (2) > (3) > (4)

2.  (2) > (3) > (4) > (1)

3.  (4) > (2) > (3) > (1)

4.  (1) > (3) > (2) > (4)

Subtopic:  Reaction Intermediates ; Preparation & Properties |
From NCERT
AIPMT - 2008
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