@a2zpractical991 SN1 Reaction Mechanism explained in the easiest way! 🔥 In this video, we will understand the SN1 Reaction Mechanism from Halogen Derivatives Class 12 Chemistry step by step. Learn carbocation formation, slow step, fast step, rate-determining step and SN1 reaction mechanism in a simple and exam-oriented way. This video is useful for Maharashtra Board HSC Class 12 Chemistry students and board exam preparation. 📚 Topic: SN1 Reaction Mechanism 📖 Chapter: Halogen Derivatives 🎓 Class: 12th Chemistry 🏫 Board: Maharashtra State Board HSC 📺 Channel: A2ZPracticals Watch the complete video and understand the SN1 mechanism in one shot. Like 👍 Share 📲 and Subscribe 🔔 to A2ZPracticals for Class 12 Chemistry and practical videos. #️⃣ Hashtags #SN1Reaction#SN1Mechanism#HalogenDerivatives#12thChemistry#Class12Chemistry#MaharashtraBoard#HSC2027#ChemistryMechanism#OrganicChemistry#BoardExam2027#A2ZPracticals 🏷️ YouTube Tags SN1 reaction mechanism, SN1 mechanism, SN1 reaction, SN1 reaction class 12, SN1 mechanism class 12 chemistry, halogen derivatives class 12, halogen derivatives Maharashtra board, 12th chemistry Maharashtra board, class 12 chemistry, SN1 reaction mechanism easy explanation, carbocation formation, rate determining step SN1, unimolecular nucleophilic substitution, nucleophilic substitution reaction, organic chemistry class 12, HSC chemistry 2027, Maharashtra board chemistry 2027, board exam chemistry, A2ZPracticals
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Video Summary
AI Generated
This video explains the chemical reaction mechanism of tert-butyl chloride using an aqueous nucleophile. It focuses on the step-by-step process of how the reactant transforms into the final product, emphasizing the role of carbocations and the kinetics of the reaction.
If we were to react to this
Who will react to this?
anewedge and child, the anewedge you will use
How should it be? Should it be aqueous anewedge?
How should it be? Aqueous. Okay?
As you take Aquous anewedge
Even then, do you know how the new edge will break?
What are you saying? Yes.
You know, this carbon plus will break in the carbon plus
And in what will chlorine break down? In minus.
The plus one together with the minus one
The one with minus, together with the one with plus. So you
Everyone knows what will happen to you, Nacl?
will come out. And the main product that you have
Listen to how the Suwan reaction mechanism works. Here's what happens with the child who is your rate operator.
The reaction occurs when the soul ascends to the higher realms during the process of the soul's journey through the draft of the afterlife. You had fallen into that state.
Because you've all read about concentration, reactants, and now look at yours
The reactant lying here, regarding which the reactant your pati sippet is handling, that one
It will precipitate only the tert-butyl chloride.
You'll say, sir, this OH is also going here
It's not going to happen here.
I will explain to you the mechanism of this thing in great detail.
Depends on tert-butyl chloride
tert-butyl chloride
Another point: how many steps is this reaction inside?
So this is a one-two step reaction.
But your second step is
How does it work?
The mechanism of the step is broken.
Constitutional Step 1
Deepak nuclear
Prested Butal Prested Chloride
Hypochlorite
What kind of a person is Kimmun?
And this slow step occurs, and it is also reversible.
When you heat this, chlorine comes out here.
So it becomes something like this
Your Til Copy
If chlorine is removed, one valency of carbon will be lost.
Though Umtu
If carbon's valency decreases by one, what will carbon form?
Karbo Katanis
So, what does your carbonyl compound become in the first step?
Now we will do the second task.
What should we do? Yes, sir, what should we do? Let's keep this number safe.
Poison Number Two, all attention gone
The carbocaine you took
Whose attack will it be on him now?
Yes, nucleophile
Okay? What will happen here with the nucleophile? There will be an attack.
Now listen carefully, child
These positives, these negatives, this planner structure
Here, two types of products can be created.
Look, Accent Two is what it is
There is an inverter configuration there.
Because Oni attacks from the front side.
Both back and front are possible here.
And this Prestep is yours, Fastep.
He will attack right here.
So you have something like a product here
What will happen when they come together?
It will be ready.
What did you see now?
Therefore, the rate of reaction depends on
Concentrate only
Above the tert-butyl chloride
Okay?
So in the first step
What can you write about the formation of carbocations?
Yes
Formation of
What can you write in the secant pass?
Attack of Nucleophiles and Carbocations
OK?
Now we see its
Yes
Let's take a look at the silent features.
What are its silent features?
Now everyone has gone, hasn't it?
I feel so lonely!
Zargale, I've got you covered—these are the star features you're looking for!
I need to download the Parthapata Starleum features.
What was it about the memory that was significant to you?
You can't speak, so let's go, all the children must know these things, next here what was it, oh
Heterolytic bond breaking had occurred, a step had taken place, and this was a reversible reaction, after which your
Who runs can do what was made of carburetor churning, the leger was made, now the child, that carburetor, carburetor churning, the calf, the ones who were there, what was it? The UCH's dough was kneaded, and that was just a tape, so that was the other one.
In the step, you have to write that nucleophilic attack occurred at the carbonyl carbon, and in the next step, you obtained the product.
See you in the next video