Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: ScarletDemiurge on November 19, 2021, 01:57:49 PM
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Hey, I'm trying to draw the mechanism for the catalytic hydrogenation of a NO2 group with Pd/C as a catalyst. I've looked at several articles (mostly "Insights into the mechanism of nitrobenzene reduction to aniline over Pd catalyst and the significance of the adsorption of phenyl group on kinetics" and "Studying the Mechanisms of Nitro Compounds Reduction (A-Review)") but they show slightly different paths to how NO2 turns into NH2. I drew the mechanism, but I'm not sure it is correct, could anyone give it a look and let me know if there's something wrong with it?
Note: I'm not sure if it's okay, but I'm assuming the hydrogen atoms that are on the surface of the Pd are able to be taken by other atoms as either protons (H+) or hydrides.
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Looks reasonable. However, nitroso (RNO) and hydroxyamine (RNHOH) functionalities have been isolated under some conditions so it might be more accepted that way?
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In my opinion wrong. Look at the step 2 and 3. Step 2 - R-N+=O and then (step 3) - R-N-O- - molecule change its electric charge.
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nitroso (RNO) and hydroxyamine (RNHOH) functionalities have been isolated under some conditions so it might be more accepted that way?
Thanks! I'll look into that.
Look at the step 2 and 3. Step 2 - R-N+=O and then (step 3) - R-N-O- - molecule change its electric charge.
That can't happen? Sorry if it's basic knowledge, I'm not that good at organic chemistry. So the molecule can't go from positive to negative (or visceversa), it needs to go through a neutral state before changing its charge?
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I just drew the mechanism again removing the change in charge and including the hydroxyamine as a precursor of nitroso.
What do y'all think about this one?