Which of the following is not chiral?

1. 2-butanol

2. 2,3-dibromopentane

3. 3-bromopentane

4. 2-hydroxypropanoic acid

Subtopic:  Stereo Isomers |
 61%
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AIPMT - 2006

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The order of decreasing reactivity towards an electrophilic reagent, for the following : 
(i) Benzene (ii) Toluene 
(iii) Chlorobenzene and 
(iv) Phenol 
Would be :

1. (i) > (ii) > (iii) > (iv)

2. (ii) > (iv) > (i) > (iii)

3. (iv) > (iii) > (ii) > (i)

4. (iv) > (ii) > (i) > (iii)

Subtopic:  Nucleophile & Electrophile |
 50%
From NCERT
AIPMT - 2007
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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 |
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AIPMT - 2008

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Which of the following compounds will exhibit cis-trans (geometrical) isomerism?

1. 2-butene

2. Butanol

3. 2-butyne

4. 2-butenol

Subtopic:  Stereo Isomers |
 66%
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AIPMT - 2009

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The IUPAC name of the compound having the formula CH≡C–CH=CH2 is :

1. 3-Butene-1-yne

2. 1-Butyn-3-ene

3. But-1-yne-3-ene

4.  Buten-3-yne

Subtopic:  Nomenclature |
 56%
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AIPMT - 2009

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In the following, the most stable conformation of n-butane is:
1. 2.
3. 4.


 

Subtopic:  Conformational Isomers |
 74%
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Decreasing order of acidic character for cyclohexanol (I), acetic acid (II), 2, 4, 6-trinitrophenol (III) and phenol (IV),  will be

1. III>II>IV>I

2. II>III>I>IV

3. II>III>IV>I

4. III>IV>II>I

Subtopic:  Acidic & Basic Character |
 53%
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Which one of the following is most reactive towards electrophilic reagent?

1.  

2.  

3.  

4.  

Subtopic:  Mechanism of Dehydration, Methanol & Ethanol |
From NCERT
AIPMT - 2011

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The correct IUPAC name of the compound 

1.  3-ethyl-4-ethenylheptane

2.  3-ethyl-4-propylhex-5-ene

3.  3-(1-ethyl propyl) hex-1-ene

4.  4-ethyl-3-propylhex-1-ene

Subtopic:  Aliphatic Hydrocarbon -Nomenclature, Isomerism & Mechanism |
 53%
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AIPMT - 2011

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The correct order of increasing bond length of 
C-H, C-O, C-C and C=C is

1.  C-C<C=C<C-O<C-H

2.  C-O<C-H<C-C<C=C

3.  C-H<C-O<C-C<C=C

4.  C-H<C=C<C-O<C-C

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 61%
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AIPMT - 2011

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