Concept: Concept: Definition of Conjugation6m
Hey guys, so now let's talk about a new concept called conjugation. Conjugation exists when three or more atoms with the ability to resonate are next to each other or back-to-back. Another way that you can think of it is that they're orbitals are overlapping. Now this idea of resonating or resonance is an old concept from organic chemistry one that you guys should all be relatively familiar with. We've all drawn a resonance structure at this point.
So you might be wondering, “Johnny, what's the difference between resonance and conjugation?” Essentially, there isn't really a difference. They're two names for the same idea. Whereas, to resonate, resonate is a verb. If you resonate something, that's an action. Well, conjugation or conjugated would be the adjective that describes that you can do that. I don't want to get too much into grammar, but basically just saying that something that is conjugated has the ability to resonate. So they're really a similar word for the same idea.
Now, what does this mean? Well, conjugation provides a highway or an electron highway for electrons to delocalize from one side of a molecule to another. And we all know that delocalization provides stability for molecules. That's something that we learned a long time ago about resonance. It turns out that these conjugated molecules, because they have the extra stability, they're going to display unique chemical reactivity that we're going to spend a few topics talking about.
Now, in another note that's pretty much unrelated to everything I just said, there's an important side not for you to know which is that the higher the level of conjugation in a molecule, the higher the UV wavelength is going to be in UV-Vis spectrometer.
Now why am I mentioning this? The higher the UV wavelength. If you guys remember, wavelength looks like that. Now the reason I'm mentioning that is because I'm really not going to spend any time talking about UV-Vis spec, but this is the only meaningful application that you really need to know about it for organic chemistry one and two, which is that as your conjugated compounds have more and more conjugation, meaning that more and more atoms can resonate together, the higher the wavelengths tend to be for this UV-Vis spectrometer. This could be a multiple choice question or it could be a free-response question that you get asked. So that's just something that I wanted to throw in there.
Now let's actually talk about the properties of the types of molecules that are conjugated. Well, we just said that three atoms with the ability to resonate have to be back to back, so what type of atoms are the ones that can resonate? Well, we all know that pi bonds can resonate. So we're going to put here one, pi bonds. Now a pi bond just doesn't have to be a double bond, it could also be a triple bond because we know that triple bonds actually have two pi bonds in them. So double bonds and triple bonds are definitely capable of resonating.
Now the other ones that are capable of resonating would be ones that have orbitals that are free to accept or donate electrons. That would be, for example, if you have basically a lone pair or an anion. I'm going to put here anion or lone pair, really depending on what the formal charges of that molecule. In terms of resonating, the idea of having a lone pair or a negatively charged anion, really they resonate the exact way. The whole deal of having a negative charge just has to do with what's the formal charge of that specific atom. So for the context of conjugation, we're going to treat these exactly the same.
So that's what happens if you have two electrons in your orbital. But we know that you don't have to always put two. Another idea is what if I just put one electron in the orbital. What's that called? That's called a radical. Radicals are also capable of resonance or conjugation. So radicals can also conjugate. And the last idea would be how about if you put zero electrons in there? Then that would be a positively charged atom. So that would be a cation.
So these are all of the types of atoms that I want you to think about when we talk about atoms that can resonate. We're just saying that here I actually have five atoms listed because I have the three different charges. I have the anion, the radical, the cation. Then I also have the two atoms from the pi bond. All I'm saying is that you need some combination of these three atoms in a row that will provide for conjugation to take place.
What we're going to do is we're going to do this practice problem and you have to identify which of the following molecules exist in a conjugated state. So go ahead and use what I talked abut earlier above as a reference and figure out which of these molecules are conjugated and which ones are not conjugated. So go ahead and do that now.
Concept: Example 1: Conjugated states4m
Concept: Concept: Review of Common Resonance Structures5m
In organic chemistry one, we learned about a position word called allylic or allyl and what allylic simply meant was that it was the position that's next to a double bond. That position is actually a little bit more important than you might think. The reason is because now we just stated that conjugation depends on three atoms in a row that can resonate. Well, double bonds typically have two of these atoms, but they're always missing the third one.
Notice this double bond. I'm going to erase this in a second. But notice this one I'm circling. It's missing. It has one, two atoms that resonate, but it's missing the third. So many times these double bonds are looking for some kind of orbital, reactive orbital to be placed on the third atom so that they can participate in resonance.
What that means is that typically, carbocations, carbanions, and radicals are usually unstable. Usually, we say these are reactive intermediates. They don't like to form. But when they're paired with double bonds on allylic positions, they become unusually stable due to conjugation. Meaning that whereas most carbocations are not very stable, the one next to a double bond will be unusually stable. It will be better than normal.
Now what I want to do is refresh ourselves, kind of on the resonance structures of these reactive intermediates because we'll be drawing a lot of resonance into this section.
Let's go ahead and start off with the simplest situation which is cations. Do you guys remember how cations move? I told you guys that cations always move with one arrow. I always talk about how if you have a cation in that allylic position, you can draw it like a door opening on a door hinge. So I just say you draw it like the door opens and now you replace the other side with a cation. Your cation and your double bond switch places and that's your resonance structure. If we wanted to show the complete structure, you would just show that this one also goes back. The cation resonance structure is the easiest one to draw.
How about basically a lone pair. Now that lone pair, if it's on a carbon, a lone pair is going to be a negative charge. Now it's not always going to be a negative charge. It just depends on what atom it is. Remember I was saying this has to do with formal charges. In this case, since it's a carbon, it's going to be what we call carbanion.
Do you guys remember how many arrows lone pairs move with? Two. They always move with two. We would actually start from the region of highest electron density just like any mechanism we've ever drawn. You would start off with these electrons moving towards the closest bond.
Now if we make that bond, we have to break a bond because we're violating the octet of this carbon right here. It already had four bonds. We're about to make the fifth one. We have to break the bond. So what we're going to get is two arrows. Make a bond, break a bond. And we're going to wind up getting something that looks like this. So negative charge here and now the double bond is on the other side. That would be applied to lone pairs, but also anything that's an anion because really they're the same exact concept.
Last one is radicals, so what if we have just one electron, a single electron next to a double bond. Now remember that radicals actually move with three arrows. They move with three half-headed arrows. So it's a little bit weird. We would start off by making part of a double bond with one. But now the double bond next to the radical breaks off into its own radical. Then we'd get one radical joining us here and the final radical being dropped off at the end where it's going to become its own standalone radical.
So now what we have is two electrons joining to make a new pi bond and that left over radical on the side. That would be four radicals. So as you can see, maybe this is like a – it's a nice little pattern, but we've got one arrow, two arrows, and three arrows. These are just ways to think about kind of categorize these resonance structures. Resonance structures are something you're still going to have to do for the rest of organic chemistry, so you have to kind of stay on your toes about that.
So that's it for this topic. Let's move on.
Dienes with alternate pi and sigma bonds are classified as ______.
E) None of These
Answer the following questions as indicated below.
A. Draw any cyclic conjugated molecule:
B. Draw any allyl radical:
What descriptive term is applied to the type of diene represente by 1,2-pentadiene?
a. Cumulated diene
b. Conjugated diene
c. Isolated diene
d. None of them
Circle any conjugated portions in the structures below.
Which structure(s) represent(s) conjugated π-bonds?
a. II and V
b. II and IV
c. V only
d. I, III and V
e. II, IV and V
Rank the following compounds in order of stability (most to least stable)
Circle the C8H12 isomer below that has the highest heat of hydrogenation.
Which compound will have the smallest heat of hydrogenation?
Which of the following compounds show conjugation?