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Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: Oso32105 on March 18, 2023, 08:41:38 AM

Title: Nitration.
Post by: Oso32105 on March 18, 2023, 08:41:38 AM

I have a problem with the nitration products of 1-benzyl-4-bromobenzene and
1-nitro-4-phenylbenzene. Can someone explain how to cleave these compounds and in which positions ortho, para or meta to put the amino group. Thank you for any help.

Title: Re: Nitration.
Post by: Hunter2 on March 18, 2023, 10:23:29 AM

I dont know what you mean with "cleave" and which amino group you talking about. From the head line you mean nitration.  Alkyl and aryl group guide to 2,4,6 position for Nitro and Nitro itself goes to 3,5 .

Title: Re: Nitration.
Post by: Oso32105 on March 18, 2023, 10:55:54 AM

Sorry, I meant the nitro group.Could you write the nitration products of these compounds I would be very grateful I need them very much ? ;)

Title: Re: Nitration.
Post by: Borek on March 18, 2023, 03:33:28 PM

Quote from: Oso32105 on March 18, 2023, 10:55:54 AM

Could you write the nitration products of these compounds I would be very grateful I need them very much ? ;)

You were already given clear hints.

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