Practice: Predict the major product of the following EAS reaction.
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|Electrophilic Aromatic Substitution||10 mins||0 completed|
|Benzene Reactions||12 mins||0 completed|
|EAS: Halogenation Mechanism||6 mins||0 completed|
|EAS: Nitration Mechanism||10 mins||0 completed|
|EAS: Friedel-Crafts Alkylation Mechanism||7 mins||0 completed|
|EAS: Friedel-Crafts Acylation Mechanism||5 mins||0 completed|
|EAS: Any Carbocation Mechanism||7 mins||0 completed|
|Electron Withdrawing Groups||23 mins||0 completed|
|EAS: Ortho vs. Para Positions||5 mins||0 completed|
|Acylation of Aniline||9 mins||0 completed|
|Limitations of Friedel-Crafts Alkyation||20 mins||0 completed|
|Advantages of Friedel-Crafts Acylation||6 mins||0 completed|
|Blocking Groups - Sulfonic Acid||13 mins||0 completed|
|EAS: Synergistic and Competitive Groups||14 mins||0 completed|
|Side-Chain Halogenation||6 mins||0 completed|
|Side-Chain Oxidation||4 mins||0 completed|
|Birch Reduction||11 mins||0 completed|
|EAS: Sequence Groups||5 mins||0 completed|
|EAS: Retrosynthesis||29 mins||0 completed|
|Diazo Replacement Reactions||7 mins||0 completed|
|Diazo Sequence Groups||5 mins||0 completed|
|Diazo Retrosynthesis||13 mins||0 completed|
|Nucleophilic Aromatic Substitution||30 mins||0 completed|
|Benzyne||16 mins||0 completed|
|EAS: Sulfonation Mechanism|
|EAS: Gatterman–Koch Reaction|
|EAS: Total Benzene Isomers|
|EAS: Polycyclic Aromatic Hydrocarbons|
|EAS: Directing Effects|
|Resonance Theory of EAS Directing Effects|
|EAS: Badass Activity Chart|
|Activated Benzene and Polysubstitutions|
|EAS: Dueling Benzenes|
|Hydrogenation of Benzene|
|EAS: Missing Reagent|
|Diazonization of Aniline|
|Diazo Coupling Reactions|
|SNAr vs. Benzyne|
|Aromatic Missing Reagent|
|EAS on 5-membered Heterocycles|
Adding a single group to a benzene ring is the first step. Now, what happens if we want to do a second reaction on that benzene. Where is it going to add? This is the question we will be answering.
Concept #1: Activity and Directing Effects
Now we know how to add a single substituent to a benzene ring using an EAS mechanism. We’re pretty good at figuring out how to add different types. You know how to add nitros and R-groups and ketones. But now the question we have to ask ourselves is what happens if you want to do a second reaction on that benzene? What if you already have something there and now you're adding a second EAS region? Where is it going to add? How is it going to add? How is that first substituent going to affect the second? It turns out that it really has a huge effect on the second one.
That brings us to the EAS of monosubstituted benzene. We’re not talking about just regular benzene. We’re talking about benzene with a substituent already. This section also is called directing groups or activity of benzene. All that is covered in this section. It turns out that that first substituent is going to really alter the election density of the benzene ring. It's going to affect the reactivity towards subsequent reactions. It’s going to affect the direction of subsequent reactions. Let's look.
The first thing that it's going to do, and it’s going to affect the activity. It turns out that we have to be, this is our first introduction to these terms of electron-donating groups or electron-withdrawing groups. These are extremely important principles in organic chemistry. They're going to come not only for the rest of this course but also for the rest of your professional career. If you want to go into anything pre-health and you need to take more classes in the sciences and in the life sciences, then you’re going to need to know about electron-donating groups and electron-withdrawing groups.
It turns out that first of all, if that first substituent that you add happens to be an electron-donating group, that means it’s giving more electrons to the benzene. Do you think that's going to make it more reactive or less reactive towards another EAS reaction? Remember, the benzene acts as a nucleophile in the reaction. The more electrons you pump into it, the more you’re going to activate it to react. They active the ring towards more reactions. If you add an electron-donating group, it’s going to want to react even more the second time.
However, if add an electron-withdrawing group, that's going to pull electrons into the outer ring making it less nucleophilic. That's going to deactivate the ring towards future reactions. That means the second reaction will be more difficult to perform than the first. Meaning it's actually less reactive than benzene by itself. But that's not it. You might be wondering, “Johnny, how do I know if something is electron-donating?” We’ll get that. Just hold on.
Also, they have directing effects because it turns out that electron-donating groups tend to be what we call ortho,para-directors. They tend to direct towards the ortho and para positions. Whereas electron-withdrawing groups tend to be meta-directors. Meaning that they direct subsequent EAS reactions to happen only at the meta positions.
Here I have a picture of these two benzenes and an electron-donating group. We would expect to add the second EAS reagent in the ortho positions or in the para positions. Hence, o,p-director. It actually means that it directs to all those positions. Whereas meta-directors, electron-withdrawing groups, they pull electrons out of the ring. They're going to tend to add in the meta positions. I forgot to draw the dipole of electron-donating. It’s going to push electrons into the ring. It directs towards o,p. Whereas electron-withdrawing groups direct towards the meta positions.
The scientific explanation of why that happens is going to be for another video. We’re not going to really talk about the scientific technical definition right now. It has to do with resonance structures. But you could also read your textbook if you want more information on that. What I’m going to focus on for right now is really just memorizing and really just knowing which groups are your electron-donating and which groups are electron-withdrawing.
Let’s move on to the chart that's going to help us with this information.
Practice: Predict the major product of the following EAS reaction.
Practice: Predict the product of the following multi-step synthesis.
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