The IUPAC name of  CH3CH=CHC≡CH is:

1. Pent - 3 - en - 1 - yne

2. Pent - 2 - en - 4 - yne

3. Pent - 1 - yn - 3 - ene

4. Pent - 4 - yn - 2 – ene

Subtopic:  Nomenclature |
 67%
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AIPMT - 2010
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The species among the following that is not an electrophile is:

1. BH3

2. H3O

3. NO2

4. Cl

Subtopic:  Nucleophile & Electrophile |
 54%
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AIPMT - 2010
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The IUPAC name of the above-mentioned compound is:

1. cis-2-Chloro-3-iodo-2-pentene
2. trans-2-Chloro-3-iodo-2-pentene
3. cis-3-Iodo-4-chloro-3-pentene
4. trans-3-Iodo-4-chloro-3-pentene

Subtopic:  Nomenclature |
 82%
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AIPMT - 2011
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Polarisation of electrons in acrolein may be written as:

1.  C+δH2=CH-C-δHO

2.  C-δH2=CH-C+δHO

3.  C-δH2=CH-CH+δO

4.  C+δH2=CH-CHO-δ

Subtopic:  Electron Displacement Effects |
 59%
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AIPMT - 2000
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The correct order of –I effect is:

1. -NR3+ > -OR  > -F

2. -F > -NR3+ > -OR  

3.-NR3+ > -F  > -OR  

4. -OR  > -NR3+ > -F

Subtopic:  Electron Displacement Effects |
 65%
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AIPMT - 1998
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The correct order of stability is:

1. 1–butene > Trans–2–butene > Cis–2–butene
2. Trans–2–butene > 1–butene > Cis–2–butene
3. Trans–2–butene > Cis–2-butene > 1–butene
4. Cis-2–butene > Trans–2–butene > 1–butene

Subtopic:  Electron Displacement Effects |
 65%
AIPMT - 2000
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IUPAC  name of  is: 

1. 2-Chloro-3-iodo-2-pentene

2. 2-Chloro-3-iodo-3-pentene

3.  2-Iodo-3-chloro-pentene

4.  None of the above

Subtopic:  Nomenclature |
 82%
From NCERT
AIPMT - 1998
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2-butene shows geometrical isomerism due to:

1. Restricted rotation about double bond

2. Free rotation about double bond

3. Free rotation about single bond

4. Chiral carbon

Subtopic:  Stereo Isomers |
 81%
From NCERT
AIPMT - 2000
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Dihedral angle in staggered form of ethane is:

1. 0°

2. 120°

3. 60°

4. 180°

Subtopic:  Conformational Isomers |
 68%
From NCERT
AIPMT - 2000
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Which of the following is most reactive towards electrophilic substitution reaction?

1. 2.
3. 4.
Subtopic:  Nucleophile & Electrophile |
 68%
From NCERT
AIPMT - 1998
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