Mark the correct option concerning the below-given structures:

​      

1. Resonating structures

2. Tautomers

3. Geometrical isomers

4. Optical isomers

Subtopic:  Electron Displacement Effects |
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Fischer projection indicates:

1. Horizontal substituents above the plane.

2. Vertical substituents above the plane.

3. Both horizontal and vertical substituents below the plane.

4. Both horizontal and vertical substituents above the plane.

Subtopic:  Hybridisation & Structure of Carbon Compounds | Stereo Isomers |

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The general formula for cycloalkanes is:

1. CnH2n+2             2. CnH2n

3. CnH2n-2              4. CnH2n+1

Subtopic:  Nomenclature |
 65%

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The IUPAC name of the compound CH3CONH(Br) is:

1. 1-Bromoacetamide           

2. N-Bromoethanamide

3. Ethanoyl bromide             

4. None of the above

Subtopic:  Nomenclature |
 69%

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The correct IUPAC name of (C2H5)4C is:

1. Tetraethyl methane         

2. 2-Ethylpentane

3. 3,3-Diethylpentane         

4. None of the above.

Subtopic:  Nomenclature |
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IUPAC name of the compound,  is:

1. 1-chloro-2,3-epoxypropane

2. 3-chloro-1,2-epoxypropane

3. 1-chloroethoxymethane

4. none of the above

Subtopic:  Nomenclature |
 59%

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The structure of cis-bis (propenyl) ethene is:

1. 

2. 

3. 

4. 

Subtopic:  Nomenclature |
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Which of the following species is paramagnetic?

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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IUPAC name of,

 is:

1. 4-Butyl-2,5-hexadien-1-al

2. 5-Vinyloct-3-en-1-al

3. 5-Vinyloct-5-en-8-al

4. 3-Butyl-1,4-hexadien-6-al

Subtopic:  Nomenclature |
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The IUPAC name of the given 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 |
 57%
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