Mobeen sajid Posted August 21, 2020 Share Posted August 21, 2020 Link to comment Share on other sites More sharing options...
Phi for All Posted August 21, 2020 Share Posted August 21, 2020 ! Moderator Note Moved to Homework Help. We don't give answers to homework questions, but we can help you work it out. What do you have so far? Link to comment Share on other sites More sharing options...
drumbo Posted September 12, 2020 Share Posted September 12, 2020 Nitration of toluene gives mono-, di-, and trinitrotoluene. The nitration of phenol with sodium nitrate gives a mixture of two isomers, from which the wanted 4-nitrophenol (bp 279 °C) can easily be separated by steam distillation. In the nitration of of benzaldehyde the product mixture is 19% ortho, 72% meta, and 9% para: I would guess that 2,4-DNP and 2,6-DNP are the dinitro isomers that would preferentially form upon nitration of 2-NP, and that the nitration of acetophenone gives m-nitroacetophenone. Link to comment Share on other sites More sharing options...
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