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In the above reaction o/p ratio will be highest when:-
(1) R=-CH3
(2) R=-CH2-CH3
(3) R=-CHMe2
(4) R=-CMe3

Subtopic:  Urea & Nitro Compound |
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Cl2 (A), Product (A) of this reaction is:

(a) 

(b) 

(c) 

(d) 

Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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 H2SO4HNO3(A)HClZn(Hg)(B),Product (B) of this reaction is:

(a) 

(b) 

(c) 

(d) 

Subtopic:  Urea & Nitro Compound |
Level 3: 35%-60%
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p-Toluidine reacts with benzene diazonium chloride to form compound, which on boiling with aq. H2SO4 give .......... products:
(1) 3
(2) 2
(3) 4
(4) 5

Subtopic:  Urea & Nitro Compound |
Level 3: 35%-60%
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Product (C) in the above reaction is:

1. 

2.

3. 

4.

Subtopic:  Urea & Nitro Compound |
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The product of the given reaction is :

Subtopic:  Urea & Nitro Compound |
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; Product (B) of this reaction is :

1.  2. 
3.  4. 
Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
Level 3: 35%-60%
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Cyclopentadiene is much more acidic than cyclopentane, because:

1. Cyclopentadiene has conjugated double bonds.
2. Cyclopentadiene has both sp2 and sp3 hybridized carbon atoms.
3. Cyclopentadiene is a strain-free cyclic system.
4. Cyclopentadienyl anion ion, the conjugate base of cyclopentadiene, is an aromatic species and hence has higher stability.
Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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 The compounds among the following that can be generated by Friedel craft acylation is/are -

I.
II.
III.
IV.
 
1. II, III and IV 2. I, III and IV
3. I and II 4. II and III
Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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The product B in the above-mentioned reaction is:

1.   2.
3. 4.
Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
 56%
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