In which form is the chlorine atom most feasibly liberated from the provided compound?

  

1. Cl

2. Cl-

3. Cl

4. Cl2+

Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
 75%
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The major product expected from the  mono-bromination of phenyl  benzoate is:

(a) 

(b) 

(c) 

(d) 

Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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(A) C8H10 KMnO4 (B)  C8H6O4FeBr2  C8H5BrO4  (C)  (one-product only)

The structure of A in the above-mentioned reaction is-

1. 2.
3. 4.
Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
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Ph-CO2HSOCl2AMe2NHB(c)Ph-CHO, unknown reagent (c) is:

1. LiALH4

2. NaBH4

3. LiAlH4(t-BuO)3

4. PCC/CH2CL2

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 |
 51%
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Cl2 (A), Product (A) of this reaction is:

(a) 

(b) 

(c) 

(d) 

Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
 69%
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; Product (B) of this reaction is :

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

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 |
 67%
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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 |
 73%
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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 |
 55%
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