Chlorine atom can be classified as:

1. Carbocation 2. Nucleophile
3. Electrophile 4. Carbanion

Subtopic:  Nucleophile & Electrophile |
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C1H2 =C2=O

The correct hybridization states of carbon atoms in the above compound are - 

1. C1= sp , C2= sp3 2. C1= sp, C2= sp
3. C1= sp, C2= sp 4. C1= sp , C2= sp2
Subtopic:  Hybridisation & Structure of Carbon Compounds |
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The correct hybridization states of carbon atoms marked as 1,2,3 in the following compound are:
\({ }^1 \mathrm{CH}_3-\mathrm{ }^2{C} \mathrm{H}={}^3{\mathrm{C}} \mathrm{H}_2 \)

1. C1= sp , C2= sp, C3= sp2 2. C1= sp2 , C2= sp, C3= sp3
3. C1= sp3 , C2= sp, C3= sp2 4. C1= sp3 , C2= sp, C3= sp3
Subtopic:  Hybridisation & Structure of Carbon Compounds |
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The correct hybridization  of carbon atoms are:    

1. C1= sp , C2= sp, C2= sp2

2. C1= sp2 , C2= sp, C2= sp3

3. C1= sp3 , C2= sp, C2= sp3

4. C1= sp3 , C2= sp, C2= sp3

Subtopic:  Hybridisation & Structure of Carbon Compounds |
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The correct hybridization states of carbon atoms in the following compound are -     C1H2=C2H-C3N
 

1. C1= sp , C2= sp, C3= sp2 2. C1= sp2 , C2= sp,  C 3 = sp3
3. C1= sp2 , C2= sp,  C 3 = sp 4. C1= sp3 , C2= sp,  C 3 = sp3
Subtopic:  Hybridisation & Structure of Carbon Compounds |
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The correct hybridization states of carbon atoms in C6H6 (cyclic compound) is/are:

1.  sp

2. sp

3. sp3

4.  All of the above

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 84%
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Structure 1.
Structure 2.
 

The Correct IUPAC names of the above structures are:

1. 2, 3–Dimethylbutanal & Heptan–4–one

2. 2, 4–Dimethylbutanal & Heptan–2–one

3. 2, 3–Dimethylbutanal & Heptan–3–one

4. 1, 2 –Dimethylbutanal & Heptan–4–one

Subtopic:  Nomenclature |
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The IUPAC name of the following compound is -

1.  4,4-Dimethyl-3-hydroxybutanoic acid
2. 2-Methyl-3-hydroxypentan-5-oic acid
3. 4-Methyl-3-hydroxypentanoic acid
4. 3-Hydroxy-4-methylpentanoic acid

Subtopic:  Nomenclature |
 63%
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The compound which shows metamerism is: 

1. C3H6O 2. C4H10O
3. C5H12 4. C3H8O
Subtopic:  Structural Isomers |
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What is the correct structure of 2,6-Dimethyl-dec-4-ene?

1. 2.
3. 4.

Subtopic:  Nomenclature |
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