Dihedral angle in staggered form of ethane is:

1. 0°

2. 120°

3. 60°

4. 180°

Subtopic:  Conformational Isomers |
 70%
Level 2: 60%+
AIPMT - 2000
Hints

Which of the following is most reactive towards electrophilic substitution reaction?

1. 2.
3. 4.
Subtopic:  Nucleophile & Electrophile |
 69%
Level 2: 60%+
AIPMT - 1998
Hints

The best method for the separation of naphthalene and benzoic acid from their mixture is:
1. Sublimation
2. Chromatography
3. Crystallisation
4. Distillation

Subtopic:  Purification of Organic Compounds |
 72%
Level 2: 60%+
AIPMT - 2005
Hints

Which amongst the following is the most stable carbocation:
 

1. 2.
3. 4.

Subtopic:  Electron Displacement Effects | Reaction Intermediates ; Preparation & Properties |
 96%
Level 1: 80%+
AIPMT - 2005
Hints

The chirality of the compound

1. E

2. R

3. S

4. Z

Subtopic:  Stereo Isomers |
 70%
Level 2: 60%+
AIPMT - 2005
Hints

The chiral centre is absent in:

1. DCH2-CH2-CH2-Cl

2. CH3-CHD-CH2-Cl

3. CH3-CHCl-CH2D

4. CH3-CHOH-CH2-CH3

Subtopic:  Stereo Isomers |
 82%
Level 1: 80%+
AIPMT - 1998
Hints

Which one of the following compounds is most acidic:
 

1. 2.
3. 4. \(\mathrm{Cl}-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{OH}\)
Subtopic:  Acidic & Basic Character |
 86%
Level 1: 80%+
AIPMT - 2005
Hints

IUPAC name of some compounds is given. The incorrect name is:

1.  : 3-Methyl-4-ethylheptane
2. : 3-Methyl-2-butanol
3. : 2-Ethyl-3-methylbut-1-ene
4. \(\mathrm{CH}_3-\mathrm{C} \equiv \mathrm{C}-\mathrm{CH}\left(\mathrm{CH}_3\right)_2 \): 4-Methyl-2-pentyne
Subtopic:  Nomenclature |
 56%
Level 3: 35%-60%
AIPMT - 2005
Hints

The structure of trans-2-hexenal among the following is:

 
1.
2.
3.
4. None of the above

Subtopic:  Nomenclature |
 83%
Level 1: 80%+
AIPMT - 1999
Hints

The chiral compound among the following is:

1. 2-Methylpentanoic acid 2. Pentanoic acid
3. 4-Methyl pentanoic acid 4. None of the above
Subtopic:  Stereo Isomers |
 73%
Level 2: 60%+
AIPMT - 1999
Hints
Links