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A compound that is formed on passing chlorine through propene at 400°C is -

1. PVC                       

 2. Allyl chloride  

3. Nickel chloride         

4. 1,2-Dichloro ethane

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
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Level 3: 35%-60%
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The reactants used in Friedel-Craft's alkylation are:                          

1. C6H6 + NH2

2. C6H6 + CH4

3. C6H6 + CH3Cl

4. C6H6 + CH3COCl

Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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In the following reaction sequence:

What is the final product, D?

1.   2.
3.    4.
Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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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 |
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In the following reaction:


Product A is:

1. 2.
3. 4.

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
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How many monochlorinated products (excluding stereoisomers) are obtained from the given reaction?
   
1. 4
2. 5
3. 6
4. 7
Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
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3-Hexyne can be converted to trans-3-Hexene by the action of:

1. H2 - Pd/ BaSO4                       

2. Li-Liq. NH3

3. H2 - Pt O2                               

4. NaBH4

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
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A compound having the shortest carbon-carbon bond length among the following is :

1. Benzene                                 

2. Ethene

3. Ethyne                                   

4. Ethane

Subtopic:  Aliphatic Hydrocarbon- Physical Properties |
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Reaction of HBr with propene in the presence of peroxide gives

1. iso-propyl bromide

2. 3-bromo propane

3. allyl bromide

4. n-propyl bromide

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
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The reaction of toluene with Cl2 in the presence of FeCl3 gives 'X' and reaction in presence of light gives 'Y'. Thus, 'X' and  'Y' are

1. X = benzal chloride, Y= o-chlorotoluene

2. X = m-chlorotoluene, Y= p-chlorotoluene

3. X = o and p-chlorotoluene, Y = trichloromethyl benzene

4. X = benzal chloride, Y = m-chlorotoluene

Subtopic:  Aromatic Hydrocarbons - Reactions & Mechanism |
 77%
Level 2: 60%+
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