 It will be less than that. Because some part of it has converted into enol. And this happens on its own. It is spontaneous. Because there are two functions, double bond and 4A. Dr. Mayer is a special type of function actually. Where two molecules exist in dynamic equilibrium. Now you can see one in all compounds we have. But here we have the two isomers exist in dynamic equilibrium. Understood? Right from this point first. Dr. Mayer is functional isonism. Dr. Mayer is a special type of functional isonism. Where the two isomers exist in dynamic equilibrium. Now we are taking this example you write down. And this is called enol. So what happens is how do you draw 2 and 3? Just you write down this number. It helps you to write down what number it is. 1, 2 and 3. So what we do? So this is as we remove one hydrant from the target and put a double bond between the two. That is what happens. This thing you have to keep in mind. The condition hydratized is what we must have S3 at least one. Okay. So what we do? Just you write down 1, 2 and 3. Right? Part of this is possible. Conditioning check. So what you have to do? You remove one hydrant from the third hydrant. Right? From this hydrant. And between the second and the third hydrant. And I showed this. Similarly for this one what is the product here? Do we have only one product? Yeah. No that's not it. Correct. This one? Another one is called different. That's it. Yes or no? Yes. It was not made in the equaling context. No. It was not made in the equaling context. No. It was not made in the equaling context. Sir, this is the single question. This one? Yes. This one? Yes. Here it is possible. Because you have one hydrant in the other. This is a conditionally satisfied. We have two hydrants in here. Right? What is this? What is this? This is a different question. Right? So with respect to this. Which one? It's alkene. We will check the stability of alkene. Which alkene is more stable? How do you check that? I check that. So we are here. How many m5 are in here? One, ten, two, three. More m5 and more GOC. Where is this? Both are possible. But in both the mediums, it's not like you will get the same product. But in the medium product. Mostly there are particles that are possibly different in different molecules. But this we call it as keto. Since the keto is the constant. Most important is keto even. They ask you that part of it is red and red. Can you tell me the difference between auto-malism and resonance? What is the difference between auto-malism and resonance? Any one difference? Five volts are? No, we don't like resonance. How can this be fixed? But here the resonance requires a planar. Yes. So I don't think auto-malism is a problem. No, it's also a problem. Is that a requirement? It's not a requirement. But its only condition is this. That this sigma converts into pi here. How you see this? CH1 hydrogen which is like this you see. CH2 and 1 hydrogen here. This sigma converts into pi. So sigma electrons involved in this reaction. In this no. Phenomenon which is auto-malism. So here we have sigma electrons involved. But resonance does not involve. So what is the difference between the two? That is the difference between the two. That is the difference between the two. Okay. Right. Now the next thing is what? It is a reaction basically. One converts into other. We have a one molecule at a different distance from. All these molecules, why it is different because they are different functional group present. So these molecules are different structures. They are the same one. Okay. Right now these are the real structure. Real structure in here. So these are the difference between auto-malism and resonance. Now you see you have auto-malism of two-malism basically. So three types. One is diode. And then pride. And then what is the next one? H. The space structure. The diode, pride and space structure. Okay. The first one is diode. Which is least important. This is not at all important. Pride and space is important. That is one example of this. Right now. And this. The shifting of hydrogen atom. And this is shifting of hydrogen atom. Takes place between first and second atom. Takes place between first and second atom. Hydrogen atom takes place between first and second. This is first and this is second. So when you draw the auto-malism structure of this, this hydrogen will shift onto the second. And it will have a double bond. It is a shifting. And edge. Double bond of two. We have positive charge here. And negative. This is the problem. Shifting of hydrogen atom between first and second. That is it. Okay. This one is least important. The second one you see. Which is pride. And in this. The shifting of hydrogen atom. The shifting of hydrogen atom. First and the second one is two and three. So when this three. Hydrogen comes over here. And this is the product. And this is the product. The second one is more stable. This one. This one. More substituted. Six. The second one is more stable. But here. Yeah. Yeah. Is there be a better shift? No. It's not like agogadiene. It's agogadiene. And if it forms, so it forms, but we will not get this. It won't form, but it forms. If it forms also here. Then it is not going to enhance. It's not possible. It's going to burn to this. So here it is. In this position. We do not have hydrogen present. Correct? So this is not a quality. Total measurement. But this carbon. It is called as imine. See double bond and inamine. Right? It's upper to lower. Double bond. And next carbon. As we do. Next carbon. As we do. Right? This has one hydrogen present. So what happens is, the hydrogen shifts from fifth carbon or seventh carbon or ninth carbon. Depending on the structure what you have. I will give you another example here. Where you can understand. So in this one, this is not this one. This hydrogen will involve incontamnism. Okay? So what happens is, 6, 7, 8, 9. Okay? So hydrogen from the ninth carbon will, you know, comes out and attacks onto the oxygen. Right? Shift by one carbon. Right? Means what? If you have double bond between first and second, then in the given part. If it is there in third and fourth, then here you will have to shift. Okay? This is what happens. One hydrogen comes over here. This double bond comes over here. This is the problem. From here it might drop. From here the hydrogen will come over here. This is state startling. Whenever we have a state startling, it is possible. But from odd number of carbon. It can be 5, it can be 7, it can be 9, it can be 8. Okay? How is it possible for some substance to distance without interfering on the molecule? What? This would all be in a mixture. It will be... See, as you know, this hydrogen has some acetic nature. Right? Because of the contribution. All that's left from it from nature. This is slightly acetic. When it is in this molecule, that's when the hydrogen comes out from that molecule. Right? So this will come out. And again it has a tendency to no, attach to the molecule. This will come out. What happens then? Stability and no. This will be back to this. Like you see, in this case, this is aromatic compound. Right? 100%. When we can say the maximum amount for most of this molecule will convert it to phenol. This is the kind of product. Okay? If you have this in both molecules, both will be in this. Right? So this one will be the major product. This one will be the standard product. So then how will it be reversed? How will it be reversed? Because like I said, this is an extra sensitivity. But see, the one thing you try to understand. When I say it's 0.2% and 100%, it is a relative, but it will be less than 0.2% on both sides. Okay? But this is a major product. But this always has to be converted to this. And this has to be converted to this. This equilibrium will be there. That is the equilibrium will be there. Right? They both convert it to each other. But at the same time. That's the main thing. This is the space thought of.