Aromatic Electrophilic And Nucleophilic Reactions1699) For conversion

1.	Aromatic Electrophilic And Nucleophilic Reactions1699) For conversion of benzene into m-nitrobromo benzene following sequence is carried out(a) Nitration followed by bromination.(c) Oxidation followed by bromination.(b) Bromination followed by nitration.(d) Oxidation followed by nitration.
Answer» Answer: a Explanation: As bromo group need to be directed at META position first step is the nitration of BENZENE as nitro group is meta directing group. Then BROMINATION will place bromo group in meta position and then REDUCTION of nitro group to make the final product meta bromoaniline.

Aromatic Electrophilic And Nucleophilic Reactions1699) For conversion of benzene into m-nitrobromo benzene following sequence is carried out(a) Nitration followed by bromination.(c) Oxidation followed by bromination.(b) Bromination followed by nitration.(d) Oxidation followed by nitration.

Answer»

Answer:

Explanation:

As bromo group need to be directed at META position first step is the nitration of BENZENE as nitro group is meta directing group. Then BROMINATION will place bromo group in meta position and then REDUCTION of nitro group to make the final product meta bromoaniline.

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Aromatic Electrophilic And Nucleophilic Reactions1699) For conversion of benzene into m-nitrobromo benzene following sequence is carried out(a) Nitration followed by bromination.(c) Oxidation followed by bromination.(b) Bromination followed by nitration.(d) Oxidation followed by nitration.​

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Aromatic Electrophilic And Nucleophilic Reactions1699) For conversion of benzene into m-nitrobromo benzene following sequence is carried out(a) Nitration followed by bromination.(c) Oxidation followed by bromination.(b) Bromination followed by nitration.(d) Oxidation followed by nitration.