@a2zpractical991 In this video, we explain Aromatic Compounds from Chapter 15 Hydrocarbons of Class 11 Chemistry (Maharashtra Board). Learn the structure of benzene, aromaticity, Kekulé structure, resonance, electrophilic substitution reactions, nitration, halogenation, Friedel-Crafts reactions, and important board exam questions.
📚 Maharashtra Board Class 11 Chemistry 🧪 Chapter 15: Hydrocarbons ✅ Aromatic Compounds Made Easy ✅ One Shot Revision ✅ Board Exam Preparation
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This lecture by Sachin Shukla explores the chemical properties of benzene, focusing on its stability and reactivity. It details the mechanisms of addition and electrophilic substitution reactions, the influence of directing groups on substitution positions, and the toxicological impact of benzene as a carcinogen.
If you carefully go through these notes with affection, your 12th grade will turn out to be very smooth.
Because this chapter is extremely important for the 12th-grade students.
And how are hydrocarbons prepared, with certain physical properties and specific reactions?
In the previous video, we had looked at it very lovingly.
And I teach children organic chemistry in such a way that they understand it thoroughly, from start to finish.
Today we will be looking at an addition reaction.
What do you mean? If you want to force an addition reaction on benzene, how would you do it?
Because Alder, I had said that benzene does not undergo addition reactions.
There are certain things, certain points, such that this reaction is possible, because chemistry always brings along mysterious elements.
Alright, let's start. My dear students, I am Sachin Sukla, conducting this lecture.
And I promised you that I would explain to you organic, meaning in a very detailed and thorough way.
And to my children who have reached up to the seventh lecture from my very first lecture, I can confidently say with assurance that they must now have begun to grasp the subject organically.
Let's start this lovely lecture, shall we?
So let's see, today our first lovely topic is the chemical properties of benzene.
In chemical properties, we basically study reactions, and so on.
I mean, let me just inform you that we study reactions specifically for aromatic hydrocarbons, which are referred to as aromatic reactions.
So how will we get to see the products?
This is what we will do in chemical properties.
So, the first topic in chemical properties that we will cover is addition reaction, which benzene does not exhibit.
Now, in the addition reaction, the first addition we will examine is the addition to chlorobenzene.
Suppose I took a benzene and performed chlorination on this benzene.
What does a child need to use for chlorination?
Tell me clearly what we take for chlorination?
Sunlight or UV light.
You can also use UV light or sunlight.
As you use it.
So, this chlorine here breaks down on a radical basis.
One thing I forgot to tell you here, the child,
The addition reaction that occurs with you,
It is a type of electrophilic substitution reaction.
Electrophilic substitution reaction
You will say, sir, what is electrophilic substitution?
Which species has a positive charge on it, okay?
And those that are electron-deficient.
What is an electron? It is electron-deficient. Okay?
Let's see.
Now listen carefully, the one who uses baby UV light or sunlight, listen carefully,
Thus, all bonds here break radially.
Now I'll tell you how they'll break.
Look, look, how was it here, there were two chlorines, it breaks apart.
Then a radical will come to chlorine, and another radical will come to chlorine here.
Because if a bond breaks, two radicals are formed.
You can break this one too, right?
Does everyone here know this? Yes, sir, we know there's hidden hydrogen here.
Now listen carefully to what I'm saying. Look, if I bring these two bottles of chlorine,
So if this bond breaks, listen carefully, everyone, listen carefully, look,
What kind of a fool are you?
This one is broken, it's okay.
That was his illness.
Jaudermal Kar Banaage
The man who built it was a madman.
Then a bond will be formed here.
So, if it's possible at this position
So, even at this position, it is possible.
So, kid, I'll use 3 molecules
Because one will be fixed here, two will be fixed here
Two will be installed here and two will be installed below.
Look at the date
Gyama
This will be the gam.
Gyama, isomers, apigenin, hecshaclorid
It's a word ball.
Gyama Hejzin
And Lindon
Linden, who is this?
If all the Jatpis are in the heart of the Jida
Upper insect site means in the fields where farming, etc., takes place, the crops that are grown there
Look at them, those who speak of Gomakasin and others, they don't keep it, so this is just a mere act of pretense.
Hey, come on, just look—this will be a completely simple reactive radical vice brick arrow.
How much did it become for two two four two three two not?
I've already told you; if you use a reducing agent there, what will happen to it?
Here's the high-grade,物资, just like I took here, okay?
And if I have to reduce the temperature of Baigin, I'll use the Niko method. I'll set it to 450 Calvin, then to 470 Kelvin temperature here—what will happen? Hchh, hchh, what kind of type is this?
What is the carbon content in the Bajin Kizhe Kiserem? So, what is present in the carbon content? Now, the river of life, speaking of the present.
What are you doing? The fast car is coming. You go, Benjaa, you go. It's a surprise here.
The argument about ozone is indeed crucial for us, as it is essential for our very existence; otherwise, as I have always been reminded, we would not have survived.
Here, here, here
We need to apply this across the double bond.
Alright, let's go with "Tik Carbon" then.
Six carbon is one two four
Five is it.
What did I say, Oh Three Molecule
They can attack anywhere because this targets only double bonds.
So I can set up a place here.
Alright, okay
And what is here a single bond彷
So, today Atis is fine, so you've seen it
What did I do, absolutely in an AGI way
You don't need to worry here.
Okay, directly to you, a simple benzene
One above, two below
One above, two below, in this manner
Show me the attachment here
Now watch what happens to your benzene.
When you subject it to ozonolysis
If you do it, this becomes yours.
Benzene Tri-ozonides
Alright
Tri-Ozonoids
Ozone is always present as Ozonoids
It gets converted now, next step
The next step is with us Zinc and H2O together
When I react, please listen carefully.
When you make Zinc react with H2O
You all know that which
Benzene is present at all its positions.
All positions of carbon
Haha, if that were the case, I wouldn't be so.
I used to write in the upper part, now with mindfulness
What is this Zinc you're talking about, you haven't even seen it?
The child will listen carefully to this: What is Zinc?
What will happen? Exactly that.
In this way, bond breaking does not occur here. In this method, a gentle bond breaking takes place—something like this, something like this, something like this, something like this, something like this, something like this, something like this. Okay, now what is there in this bond breaking, child?
Tell me which CA this CA connects to.
There was a Kani Kri in this CA Ipm.
So I see the connection.
Shaum Feitar's object is here.
It will look like a shawl, not a scarf.
A renowned poet and a distinguished scholar
I guess it's right next to Garuro's Lissi Mall.
What happened to the oxygen? Look, CHO, CHO
Both have slipped away; the entire thing has gone.
Look here, look at this!
Let me show you one from another pen, look from the dehna perspective
Look, this whole thing is like this
And this entire hope has shattered and left from here
It's going out, look, it's splashing
Look, this one has also broken, this one has also broken, this one has come loose
This oxygen, this oxygen
reacts with ZN to form ZNO
So, how many molecules can come out like this?
One of them slipped away, and look at the other one.
You can exit from here, look
These CHO, these CHO
It can exit from here, two molecules
Another one can come out, these CHO
And this is CHO
One, two
And these three
What could possibly happen here from here?
He can come out, look, three CHO, look here, the child
Look here, these three CHO's, what will happen to these three from here outside?
So, what happens to our 3 molecules of CHO here?
It comes out, what happens to the 3 molecules of CHO here?
It comes out, then 3 CHO
3 CHO What happens here? Just get out already
It is also commonly known as glyoxyl.
Glyoxyl compounds correct
Right? Then look carefully.
Look, the bond is breaking down.
The bond is breaking, it's coming out.
So CHO came out from here 2
Get out from here, CHO, get out from here, CHO
Say it out loud: What happens to ZNO, ZNO, ZNO when oxygen is involved, ZNO, ZNO, ZNO
He will fill out the ZNO form as long as he needs to.
ZNO, ZNO, ZNO
ZNO will also be held here three times.
What could be another name for it?
ETHANE, 1, 2, DRY
Very easy reaction, please fix this
You've already done it; first, perform ozonolysis.
O3 molecules, create temple-like structures
One on top, the other two below
One O above, two O below
Later, remove CHO from CHO.
Alright, let's move on to the next one.
If it's required, I'll show you right here.
that benzene shows electrophilic substitution reaction
that you will find out in Resonance
And the electrophile group we have
like Cl, Br⁺, NO₂⁺
SO3H+, and R+, okay
All of this is your Electrophile Substitution Reaction
show them
Next
Look, I'm going to halogenate it for you
I will show you the substitution reaction on benzene.
And the example I am considering in it is
Chlorobenzene, okay
I'll do chlorination, if
If I carry out the chlorination of benzene, what will I get?
It matches, okay, so benzene's
When performing chlorination, pay attention to
Hear me out, first call this an Electrophile
What does it do?
This is your electrophile group.
A positive charge, one by one.
This is your electrophile group, okay
Alright, if you don't understand
So I'll tell you about bromination, it's very
I can explain it clearly, look, now I
I will perform bromination on benzene.
At any position of carbon,
Craig will attack at the position of benzene if he does so.
Bromine will come here today.
And the H that comes out from there, the second one
What will be made with Opal Brax?
What is the name of Achyut Kishore?
If we go from 30 benzene to 75 benzene
Will you make it or not?
Will you make it or not, child
Saharin, you will speak
What is Clotrimazole?
We can do tooling with it.
A and M Meng is required, and Ben Raf is required.
Why can I tell you?
Why do you react when you see it?
So this reversible reaction shows
reversible reaction after product formation
After that, back again
It moves from the product side to the reactant side with such rapid reactivity.
When will your HI become a reality?
So, in the big one, it should be in the middle, the center of the dikhna should be the focus.
He complains about his own fate.
Iodination not done
If the rat has gone, then iododhya is not a servant.
It's fine here, let's proceed with the next reactions.
With access to one chlorine, benzene gives hexachlorobenzene. You have one chlorine.
Just took it, if I had chlorine in my access, like, my stuff, I have this here
If Sara sealed it tightly, what could possibly happen here? Could you please tell me, okay? We're good.
Here we will use An Hae Dars El Seil, which is also a type of Luis Acet Sei.
Remember, if you use a one-dolé molecule like Cl₂, you'll get chlorobenzene, but if you use excess chlorine, you'll get hexachlorobenzene. Here you go—fun organic chemistry!
Doubts constantly torment me, making me feel very restless and anxious.
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If you don't break this HNO3, there are two ways.
We might meet. One is OH, and the other is
NO2+. Okay, remember this. Never break HNO3
So what happens in OH and NO2? It undergoes breakdown. That's exactly what happens.
You're talking about the nitration reaction. Let me explain nitration to you.
I'm giving you the reaction very well here
But look. Suppose you carry out nitration on benzene.
Done. Nitration using HNO3. This is a nitration reaction.
It is a mixture. Whenever HNO3 comes, it is mixed with it.
Bro, here it comes, and its name is Concentrated H2SO4. This
The nitrating mixture consists of concentrated HNO₃ and concentrated H₂SO₄.
You all know how HNO3 will break down, right? You know, sir.
OH minus and NO2 plus. Come on, tell me about benzene.
Which reaction is possible above? Sir, you just mentioned it.
Only a positive electrophile can react on top of it.
Alright, react with the electrophile.
Here, further ahead, your NO2 and the H that came out combine with this OH.
What will it make? H2O. Tell me, what should I call this?
Nitrobenzene. Sir, you won't be giving the theory written down.
Son, can you write the theory? What else could I possibly tell you about this?
Has achieved mastery in the reaction of Benzene with Concentrated HNO3
in the presence of concentrated H₂SO₄ to form this.
Add some heat here too, okay?
Alright, did you figure it out? Nitration mixture—concentrated HNO₃.
Next, they increase toward sulfonations.
You all know H2SO4.
And if you break down H2SO4, one of them breaks into your OH-.
And there is one SO3H+ of yours. That's exactly what we need.
That's exactly what will cause sulfonation. Okay, let's go.
Look, if you have a benzene group, and if you use concentrated H2SO4 here,
The Catalyst that needs to be used along with this is Fuming.
Fuming H₂SO₄. Okay?
Now tell me, how will this break? Come on, tell me quickly, how will it break?
Sir, you just mentioned OH- and SO3H+.
The plus guy, just take him anywhere and hand him over, buddy, okay?
What would it become if taken anywhere and turned into dough?
SO3H+, the H that comes out—will it form H2SO4 by combining with this OH?
Its name is Benzene Sulfonic Acid.
You all have realized one thing, dude, Chlorine Nation has become a reality.
CL2, Gromi Nation remained, BR2, Nitration remained,
H2SO4, okay?
Alright, let's move on to the next reaction.
Next reaction is the Friedel-Crafts alkylation reaction, which is also present in your twelfth grade, child reaction.
It's very important to observe it carefully, even in the twelfth grade.
This comes up in exams quite often, you know.
And this reaction will come in your 11th, it also comes in 12th, okay.
Look closely, how can you understand this reaction? Look very carefully.
If I, the children above benzene, listen carefully,
If I perform Friedel-Crafts alkylation on benzene
In alkylation, one thing to remember is this
Use CS3CL
And Firdal Craft has given Catlis.
Never forget that catalyst, kid—it's used everywhere.
Will you ever forget this is not anhydrous AlCl₃?
Whenever Firdal Craft Baba comes, bring Atma Catalis with you.
And the cat's name is Unhydrous Al-Cl-3
Alkylation, then what will you do about it?
CS3CL because the second one is also a part
Now, look what this guy is doing with anhydrous AlCl₃
He won't let it break.
So this will break down.
CS3 Plus and CL Minus
Because it keeps attracting this along with it.
Positively charged
Everyone knows, Brother
As he will rise above benzene
Then it will connect above the benzene.
What?
Yes!
CS3
After that, the H that will come out
What will it form with the other cell?
SCL
All children know their names.
Its name is
Tolion
Methylbenzene
You know, don't you?
Which guru is this?
Electro File
What kind of guru are you?
Electro File
That's exactly what happens here.
So, shall I fiddle everyone?
Does everyone understand the alkylation reaction?
Alright, I'll tell you the truth right here.
Look here, it's a relaxation.
Jago Bijnin ka Bijnin rakha kaha, as it is
What chance do you have in this easy life?
A simple group of people, you are in the functional group
It has been taught about Asayal, this is yours
anhydrous
AlCl₃
What is the function of this?
It's his job to break the child.
How will you break it?
One to plus, the other to
minus in
Where will the one who eats fruits go?
You'll go there, dude
OK
Where will the fruit seller go?
He will go there.
Here it is, the plus version has arrived, right where he needs to go.
And associated with it is CS3.
And the one that comes out with it will be H.
What will it form with the other CL? SCL
Now I'm your IUPSC name
Tell me two things, I'm listening, two
One phenyl, then one phenyl
Here, non
Because this is a ketonic group, it is non-
It's ketonic, right? Look, RC double bond
CL, it's a one-piece finial, look here
Never mind the ring, never mind the group,
It has another name, this one
They're acetone, and these are phenyls.
So, Aceto, Finz
Because the child
This is the group, and
In the group, you are the one who is being called.
You'll have to apply the paste, then acetate
Phinj is a surname.
Ace it, and this will be your finale.
So since this is for acetofenan, right now we're doing back-to-back
What is a scientific best reaction? Well, the Friedel-Crafts reaction is one.
And here, if you want to substitute any group here, just add any substitution here; whatever you remove will be high dose—look here, if you have any benzene and
If you're making some substitutions here, then from here onwards
What will happen to you with hydrogen?
This hydrogen will come out, that's it, your hydrogen
It will be replaced when the substitution group
When preparing, the mono substitute
Substitution Group
A monosubstituted group reacts with an electrophile.
Because only electrophiles can attack benzene
Let's see here
Here is your substituted group
Now, if I carry out an attack by any electrophile on this substituted group above
I attack any electrophile.
So, there's a possibility of finding multiple products here.
What are the possibilities?
First, let me explain to you about ortho, para, and meta.
In the child case group, where the substitute is present, it is located just in front of the para-paras.
What is below the first para's ajuba and below ortho and ortho?
Okay, now look here
If I go to see here, then in the first case
If this is a substituted group here, then an electrophile group can attach here.
Or, the electrophilic group there can also undergo substitution here.
Alright
So, what are the meta-directing electrophile and ortho-directing electrophile groups doing here?
React
What are the other possibilities? Tell me.
Possibility number 2
What is possibility number 2?
possibilities
Number 2 is here, right here.
Now, this electrophile here
This group can attack Meta.
But Meta is here too, on this side as well.
Meta Okay, so this
He can attack here, here.
What is the third case becoming here?
I'll also mention the third case here.
that this
Electrophile group is this one you have
It can also attack from the para position.
So here it is
After Monosubstitutes
Any electrophile attacks
So there are three possibilities that three
Different types of products are available here for us.
Can be obtained as Ortho, Meta, and Para
Alright, then this will be yours.
Ortho Product This is yours
Will it happen? Everyone, speak up
Meta Product and this is yours
What will happen? Say it.
What will happen to Product Para?
Look at your Yes Para Product now
on the basis of this
attachment means the electrophile
Here it is attached.
two types there are two types
How is our yes child
Ortho and Para Directing Groups
Because this is the very group
carry out
Any incoming group that you have
What needs to be done for Ortho and Para?
What do you need to do on Ortho and Para?
It should be attached, like this, look here
As I teach you a resonance here
If you have
So now, look, this is the thump of resonance
Some things will be explained here.
Resonance should come to everyone, okay? Just look at it like this.
Okay, let's go.
I'll start the resonance, then I'll tell you how it works.
They influence; look at these positions
As you start the resonance, this electron will move this way
If the electron shifts over there, the child will...
So, it will have a deficiency of one electron.
So this will be the bull and the child here.
If a bond is formed, the valency of this carbon will become 5.
Count it, see, shall I count it?
And a bond was placed on him; how much has it become? Five
Will it go or won't it go, man?
No, it won't work. Okay, then what will happen immediately?
Like this group here, don't attack, I mean
Bond makes it immediately this
It's a pi-bond, isn't it? It comes out now.
If the pi-bond protrudes outward then
How many electrons are there in a bond? Two electrons—one electron stays on this side, one electron stays on that side. Now, if both electrons come to the same carbon atom, what will happen to that carbon?
What is minus? The next step is increasing.
Will the response be negative?
Is Apple now safe?
He will donate here again.
and he will again turn evil
I will go far again
What will happen
I went inside.
and he went out again
What to do
What will you do?
His response
I called him off
I don't know
From this response, we are learning that
that your ortho, para, and ortho para
What kind of charge is the child facing?
Positive charge
Who will take the lead on this?
A negative charge here.
The cow gives milk when it is pregnant.
The most expensive designer dining set ever made is the Jade Dynasty Dining Set by Alí Designer Dining
Gadhenrash Jada A Tale Feel Ka Jata Pyakrata Japny Janaki
Meta
Vaccines, except for Meta Position
So, you all have to remember this little trick
Ortho para and ortho meta have negative charges.
So, what do electrophiles do? They attack.
So much for that simple thing ~~ all the children have gone missing
We will make it, the dish of Drodavishan, the pickle of Acharoag
Just one jump, and the drug has already gone.
Oh, the rauretoe fund is plus
Baronemonium Plus
Carbonyl compound
Am I a genius?
You understand, NFT has become garbage
Candle
He told me about the incident, and I didn't know anything about it.
The ones who will teach the metta are the Jains!
How are positive charges generated, explain why oxygen
Oxygen is more electronegative; check in pyridine.
Later comes the carp, first comes the carp, so when you go left to right
This Gurb is on meta position for any reaction
Force you to react
If you happen to see a grub with a charge position like this somewhere
I'll tell you how to do it.
Come on, let's see here
Let me explain one of the resonance theories to you here.
So you'll understand, man, if this position is for the charge-based grub
Cyanite is also your example, okay
It's your positive, and what happens to you is your positive.
It's negative, right? Even if it's placed somewhere like that.
Only the Meta Directive Group can respond; okay, let me give you
Let me tell you about your own two.
Child, this is your own two.
And this becomes your positive.
Reaction here of this kind
Watch what happens now—this is positively charged.
This is a negative charge.
Look, now from here this electron
What will starting to pool do?
This electron density is negatively charged.
The child is more electronegative than oxygen.
That's why I'm taking this bond with me
What does pooling do when it starts?
Take all these bonds with you
Once it starts polarizing, this bond shifts this way.
And this bond goes this way.
So now it's starting to look something like this
Now look, this bond went this way, this bond went this way.
So oxygen took an electron
This will be a positive one.
Once this bond breaks, the child loses this carbon.
So what happened, plus the rest I'm writing as it is
Now that it has become plus,-domain, what will plus do?
Next step
Look at the next step
It should become neutralized.
So this will attract it this way.
If the child attracts this
So a bond will be formed here.
But what charge will be applied above this?
The positive charge will arrive today.
It will no longer want a positive charge.
It will pull back.
And it will pull it back this way.
So it will start to look something like this
I took it back from there.
What are you realizing here now?
What is becoming evident here?
If all of this is grouped together
So the child who is yours ortho
Something else will come up on top of this.
So, will someone from the electric file come to attack them?
A positive charge
Will Ortho and Para come to this Tom Attack?
No, it's not this tom.
ortho, para, and ortho
electron density has decreased
It has already arrived, so what will happen to any incoming group if it comes?
incoming group incoming group attack on
Okay, now you understand it
why are they attacking the incoming group's metaposition?
What has the electron density of the orthoposition of para-position become?
has already decreased, which is why any incoming group coming from outside
Come on, this is the best explanation of resonance where you are
It becomes clear which one is the negative charge and which is the positive charge.
Group attack where is going to be conducted next topic is our carcinogenicity and
The toxicity of benzene—okay, look, the resonance I taught you about, that one
Where you've now understood that, dude, chlorine, bromine, and
if there is an iodine and also a methyl group somewhere connected there
Ortho, para, and ortho-p orientation occurs with any electrophile.
But if your group is a positively charged group attached to benzene
As in anode to all compounds of the carbonyl group, such as aldehyde, ketone,
carboxylic acid, cyanide, and
If this entire group is connected somewhere
They direct benzene to the meta positions.
Because when reacting, ortho, para, ortho lead to the formation of a positive charge
Just take a quick look at this, and then you'll understand it very clearly.
So, is benzene toxic and carcinogenic?
Yes, benzene is both toxic and carcinogenic because of it.
Cancers are caused by polycyclic aromatic compounds.
such as fused aromatic compounds having two rings fused together
If their incomplete combination is made, such as tobacco,
coals and petroleum are also highly carcinogenic
substances come out, which are our liver, lungs, and
They can cause cancer in our bodies, okay, next point
is that if benzene enters the liver, then it does
It becomes oxidized and forms epoxides, which form.
The epoxide that is benzopyrene reacts with glutathione
If it forms epoxy diol, then I won't write these points for you—I'll write them myself.
Do you know what benzopyrene forms when it reacts with smoke?
epoxy, epoxy diol remains, and this epoxy diol is very dangerous
What is epoxy diol? It is highly dangerous.
It causes mutations in our DNA.
causes mutation in DNA
it causes mutations in DNA and
It is so dangerous
It also causes mutations in our DNA, and when our cells begin to grow
That's exactly what cancer cells are—uncontrolled growth of the cancer cells.
The mutation gets activated, after which cancer cells begin to form.
DNA is so dangerous that it becomes hazardous to our bodies.
Those chapters, I read them with great heart for you, kids.
I want you to please, if you have this last, if you have this last
If you're looking at part, please go from part 1 to part 7
The child is seen so well because I made the video from the heart for you.
If you just take a look at these chapters, I'll tell you in 11
I'm giving it to you that if you love these chapters completely in 11
Each of your chapters has been placed in a playlist. Please take a look at them, I beg you.
Because I'm very dedicated to you, I'll stay focused until your chemistry doesn't suffer anymore. Thanks, see you later.
Thank you, but Banajara has made a video, and when you watch the video in full, you'll realize it's meant for you.