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Toluene, when treated with Br(2)Fe, give...

Toluene, when treated with `Br_(2)Fe`, gives o and p-bromotoluene, because the `CH_(3)` group-

A

is ortho and para directing

B

is meta directing

C

deactivates the ring by hyperconjugation

D

deactivates the ring

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The correct Answer is:
To solve the question regarding the reaction of toluene with `Br2Fe`, we need to analyze the structure of toluene and the effects of the `CH3` (methyl) group on the benzene ring. Here is a step-by-step solution: ### Step 1: Understand the Structure of Toluene Toluene is a methyl-substituted benzene, which can be represented as follows: - The benzene ring has six carbon atoms and is denoted as C6H5. - The methyl group (CH3) is attached to one of the carbon atoms of the benzene ring. ### Step 2: Identify the Effects of the Methyl Group The methyl group is an electron-donating group due to its +I (inductive) effect and hyperconjugation. This means: - The methyl group increases the electron density on the benzene ring. - It activates the ring towards electrophilic substitution reactions. ### Step 3: Determine the Directing Effects In electrophilic aromatic substitution reactions, substituents can be classified as ortho/para-directing or meta-directing: - The methyl group is ortho/para-directing because it stabilizes the carbocation intermediate formed during the reaction at the ortho and para positions relative to itself. ### Step 4: Reaction with `Br2Fe` When toluene is treated with bromine in the presence of iron (Fe), the following occurs: - The bromine acts as an electrophile. - Due to the ortho/para-directing nature of the methyl group, bromination occurs predominantly at the ortho and para positions. ### Step 5: Conclusion The reaction of toluene with `Br2Fe` results in the formation of o-bromotoluene and p-bromotoluene. The methyl group does not deactivate the ring; rather, it activates it and directs the incoming bromine to the ortho and para positions. ### Final Answer Toluene, when treated with `Br2Fe`, gives o-bromotoluene and p-bromotoluene because the `CH3` group is ortho/para-directing. ---
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ALLEN-ALKYL AND ARYL HALIDE-EXERCISE-05 (B)
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  2. Benzyl chloride can be prepared from toluene by chlorination with

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  3. Toluene, when treated with Br(2)Fe, gives o and p-bromotoluene, becaus...

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  4. A solution of (+)2-chloro-2-phenylethane in toluene racemises slowly i...

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  5. The order of reactivities of the following alkyl halides for an S(N^2)...

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  6. Which of the following has the highest nucleophilicity ? F^(-) OH^...

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  7. An S(N)2 reaction at an asymmetric carbon of a compound always g...

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  8. The number of isomers possible for the molecular formula C(2) FCIBrl i...

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  9. In the presence of peroxide, hydrogen chloride and hydrogen iodide do ...

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  14. CH(3)CH(2)CHCl(2) overset(Aq.KOH)rarr?

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  15. Draw the stereochemical structure of the product in the following reac...

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  16. Given reasons:

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  17. An alkyl halide (A) of formula C(6)H(11)Cl on treatement with potassiu...

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  18. With would be the major product in each of the following reactions?

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  19. The following compound on hydrolysis in aqueous acetone will give .

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