WebWe would like to show you a description here but the site won’t allow us. WebSo let's show the results of our acid-base mechanism. So on the left, right, the lone pair on the left of the oxygen didn't do anything. The lone pair on the right of the oxygen picked up a proton, formed a bond, and so we get this with a plus one formal charge on the oxygen.
The Sulfonation of Benzene - Chemistry LibreTexts
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18.4 Aromatic Nitration and Sulfonation - Chemistry LibreTexts
WebOrganic Chemistry I: Professor Carl C. Wamser: Exam 2 Answer Key: Chem 334 - Fall 2004. 1. (15 points) Write complete names for each of the following, including stereochemistry if it is specifically shown. ... (15 points) The same two products arise, in the same ratio, from acid-catalyzed hydration of either 1,2-dimethylcyclohexene or 1,6 ... WebDraw the major organic product formed when the compound shown below undergoes a reaction with fuming H2SO4. This problem has been solved! You'll get a detailed … WebThe mechanism for nitration of benzene: Step 1: Nitric acid accepts a proton from sulphuric acid and then dissociates to form nitronium ion. Step 2: The nitronium ion acts as an electrophile in the process which further reacts with benzene to form an arenium ion. Step 3: The arenium ion then loses its proton to Lewis base forming nitrobenzene. Sulfonation of … chris corr rayonier