The correct structure of 3,3-dimethyl butyne is-
1. 
2. 
3. 
4. 

Subtopic:  Nomenclature |
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The IUPAC name of the compound, 

 CH3CH2CHCONH2
                           |
                           CH3 is-

1. 2-Ethylbutanamide

2. 2-Methylbutanamide

3. 1-Amino-2-methylpropane

4. None of the above

Subtopic:  Nomenclature |
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The IUPAC name of the compound,

      is:   

1. 1,2-Dimethyl-2-butenol

2. 3-Methylpent-3-en-2-ol

3. 3,4-Dimethyl-2-buten-4-ol

4. 2,3-Dimethyl-3-pentenol

Subtopic:  Nomenclature |
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 The compound is an example:

1. aromatic compound                 

2. heterocyclic compound

3. annulene                               

4. xanthates

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The IUPAC name of the compound

1. 2-Iodo-3-chloro-4-pentanoic acid

2. 4-Oxo-3-chloro-2-iodopentanoic acid

3. 4-Carboxy-4,3-chloro-2-butanone

4. 3-Chloro-2-iodo-4-oxopentanoic acid

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The IUPAC name of the given compound is:

1. 4-Butylpent-2,4-dienal
2. 5-Vinyloct-3-en-1-al
3. 5-Vinyloct-5-en-8-al
4. 3-Butyl-1,4-hexadien-6-al

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Isobutyl chloride is-

1. CH3CH2CH2CH2Cl

2. (CH3)2CHCH2Cl

3. CH3CH2CHClCH3

4. (CH3)3C-Cl

Subtopic:  Nomenclature |
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The compound that has an isopropyl group is-

1. 2,2,3,3-Tetramethylpentane

2. 2,2-Dimethylpentane

3. 2,2,3-Trimethylpentane

4. 2-Methylpentane

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The IUPAC name of the above mentioned compound is - 

1. 3-Methylcyclobut-1-en-2-ol 2. 4-Methylcyclobut-2-en-1-ol
3. 4-Methylcyclobut-1-en-3-ol 4. 2-Methyl cyclobut-3-en-1-ol
Subtopic:  Nomenclature |
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A paramagnetic species among the following is-

1. A carbocation 2. A free radical
3. A carbanion ion 4. All of the above
Subtopic:  Reaction Intermediates ; Preparation & Properties |
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