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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 |
 87%
Level 1: 80%+
AIPMT - 2005
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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
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The structure of trans-2-hexenal among the following is:

 
1.
2.
3.
4. None of the above

Subtopic:  Nomenclature |
 82%
Level 1: 80%+
AIPMT - 1999
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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
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The number of chiral carbons in β–D–(+)– glucose is:

1. Six

2. Three

3. Four

4. Five 

Subtopic:  Stereo Isomers |
Level 3: 35%-60%
AIPMT - 2004
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The compound that is least reactive towards nucleophilic substitution reaction is:

1. CH2=CHCl

2. CH3CH2Cl

3. CH2=CHCH2Cl

4. (CH3)3CCl

Subtopic:  Nucleophile & Electrophile |
Level 3: 35%-60%
AIPMT - 2004
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R and S enantiomers differ in:

1. Chemical properties

2. Solubility in achiral solvent

3. Rotation of plane polarised light.

4. Dipole moment

Subtopic:  Conformational Isomers |
 86%
Level 1: 80%+
AIPMT - 2000
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The IUPAC name of the following is: 
CH2 = CH – CH2 – CH2 – C ≡ CH

1. 1, 5-Hexenyne 2. Hex-1-en-5-yne.
3. 1-Hexyne-5-ene 4. 1, 5-Hexynene
Subtopic:  Nomenclature |
 89%
Level 1: 80%+
AIPMT - 2002
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 and  are-

1. Resonating structures

2. Tautomers

3. Geometrical isomers

4. Optical isomers

Subtopic:  Structural Isomers |
 73%
Level 2: 60%+
AIPMT - 2002
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Geometrical isomers differ in:

1. Position of the functional group.

2. Position of atoms.

3. Spatial arrangement of atoms.

4. Length of the carbon chain.

Subtopic:  Stereo Isomers |
 83%
Level 1: 80%+
AIPMT - 2002
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