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

Subtopic:  Nomenclature |
 78%
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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 |
 83%
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 The compound is an example:

1. aromatic compound                 

2. heterocyclic compound

3. annulene                               

4. xanthates

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Which of the following species exhibits paramagnetism?

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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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 |
 75%
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The compound obtained by heating a mixture of primary amine and chloroform with ethanolic potassium hydroxide (KOH) is                                                                          

1. an alkyl isocyanide

2. an alkyl halide

3. an amide

4. an amide and nitro compound

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Nitrobenzene on reaction with conc. HNO3/H2SO4 at 80-100°C forms -

1. 1,2-Dinitrobenzene

2. 1,3-Dinitrobenzene

3. 1,4-Dinitrobenzene

4. 1,2,4-Trinitrobenzene

Subtopic:  Aromatic Hydrocarbons - Reactions & Mechanism |
 59%
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Ethyl chloride is converted into diethyl ether by -                                                  

 1. Wurtz reaction                           
 2. Grignard reaction
 3. Perkin's reaction                       
 4. Williamson's synthesis

Subtopic:  Mechanism of Reactions |
 62%
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Consider the following reaction,

PhenolZn-dustXAnhy.AlCl3CH3ClYAlk.KMnO4

The product Z is                            

1. toluene

2. benzaldehyde

3. benzoic acid

4. benzene

Subtopic:  Isomers & Reaction Mechanism |
 82%
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In this reaction, CH3CHO + HCNCH3CH(OH)CNH.OHCH3CH(OH)COOH an asymmetric centre is generated. The acid obtained would be                                                                      

1. 50% D + 50% L-isomer

2. 20%D + 80% L-isomer

3. D-isomer

4. L-isomer

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