When toluene is treated with a mixture of excess sulfuric acid and nitric acid at high temperature, a compound is obtained that exhibits only two signals in its ¹H NMR spectrum. One signal appears upfield and has an integration of 3. The other signal appears downfield and has an integration of 2. 18.85a1 * Incorrect. Draw the structure of the compound. To save time drawing, an abbreviation can be used for a nitro group. To search for Abbreviated groups, use the toolbar button below the list of atoms, or press the space bar.

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Chapter1: Chemical Foundations
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Draw the structure of the compound that started as toulene.

When toluene is treated with a mixture of excess sulfuric acid and nitric acid at high temperature, a compound is obtained that
exhibits only two signals in its ¹H NMR spectrum. One signal appears upfield and has an integration of 3. The other signal appears
downfield and has an integration of 2.
18.85a1
X Incorrect.
Draw the structure of the compound. To save time drawing, an abbreviation can be used for a nitro group. To search for
Abbreviated groups, use the toolbar button below the list of atoms, or press the space bar.
CH3
O₂N
Edit Drawing
Transcribed Image Text:When toluene is treated with a mixture of excess sulfuric acid and nitric acid at high temperature, a compound is obtained that exhibits only two signals in its ¹H NMR spectrum. One signal appears upfield and has an integration of 3. The other signal appears downfield and has an integration of 2. 18.85a1 X Incorrect. Draw the structure of the compound. To save time drawing, an abbreviation can be used for a nitro group. To search for Abbreviated groups, use the toolbar button below the list of atoms, or press the space bar. CH3 O₂N Edit Drawing
Expert Solution
Step 1

The substitution of nitro group to an organic compound is known as nitration reaction. In nitration reaction, nitronium ions acts as the electrophile and the reaction is an electrophilic substitution reaction.

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