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.
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.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw the structure of the compound that started as toulene.
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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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