subject
Chemistry, 19.03.2020 08:57 cristianTalonzo

Both pyrrole and pyridine are aromatic compounds, and undergo electrophilic aromatic substitution (EAS). Using a resonance argument, predict the regiochemistry of EAS on both pyrrole and pyridine. As part of your argument, you must draw resonance structures for the arenium ion leading to each possible regiochemistry, and compare the stabilities of the resonance hybrids. In addition, make a reasoned statement about whether you think each one would react faster or slower than benzene and why.

ansver
Answers: 2

Another question on Chemistry

question
Chemistry, 22.06.2019 01:30
Phosphorous acid, h3po3(aq) , is a diprotic oxyacid that is an important compound in industry and agriculture. the values of phosphorous acid are 1.30 6.70 calculate the ph for each of the given points in the titration of 50.0 ml of 1.5 m h3po3(aq) with 1.5 m koh(aq) .
Answers: 3
question
Chemistry, 22.06.2019 18:00
Which three statements represent the benefits of performing experiments using computer simulations?
Answers: 3
question
Chemistry, 22.06.2019 18:30
Which of the following nuclei would be the least stable a 2 protons, 2 neutrons b 1 proton 1 neutron c 1 proton 3 neutrons d 1 proton 2 neutrons
Answers: 3
question
Chemistry, 23.06.2019 00:00
How is the way a mixture is combined different from how a compound is combined?
Answers: 3
You know the right answer?
Both pyrrole and pyridine are aromatic compounds, and undergo electrophilic aromatic substitution (E...
Questions
question
Computers and Technology, 15.12.2020 19:50
question
French, 15.12.2020 19:50
question
Mathematics, 15.12.2020 19:50