Benzene reacts with CH3Cl in the presence of anhydrous AlCl3 to form:
| 1. | Toluene | 2. | Chlorobenzene |
| 3. | Benzylchloride | 4. | Xylene |

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The reagent used in the above conversion is:
1. Cr2O3
2. Alc. KOH
3. Red hot Fe
4. NaNH2/liq.NH3

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The reaction of toluene with Cl2 in presence of FeCl3 gives ‘X' and the reaction in presence of light gives 'Y'. 'X' and 'Y' are respectively:
| 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= Benzyl chloride, Y= m-chlorotoluene |

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RCOCl and are used in the Friedel-Crafts reaction.
The electrophile among the following is:
1.
2. RCOCl
3. O
4.

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The Product (B) in the above-mentioned reaction is:
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |

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Nitrobenzene on reaction with conc. HNO3/H2SO4 at 80-100C forms:
1. 1,2-Dinitrobenzene
2. 1,3-Dinitrobenzene
3. 1,4-Dinitrobenzene
4. 1,2,4-Trinitrobenzene

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Arrange the following compounds in increasing order of their reactivity toward electrophilic aromatic substitution reactions.

| 1. | III < I < II | 2. | III < II < I |
| 3. | II < I < III | 4. | II < III < I |

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Which of the following compounds undergoes bromination of its aromatic ring (electrophilic aromatic substitution) at the fastest rate?
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |

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