chemistry-class-12-unit-11-chapter-02-phenols-l-2-6-3tra2uw1w8q

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Phenols</B></primary></p>
<hr>
<main>
<div style='float: left; width:60%;font-size:22px;text-align:left'>
<ul>
<li>
<p><strong>Reimer-Tiemann reaction</strong></p>
</li>
<li>
<p>It is ortho formylation of phenol</p>
</li>
<li>
<p>It doesn’t requried anhydrous condition</p>
</li>
</ul>
</div>
<div style='float: right; width:40%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/8946c647-b715-4b5f-9385-cbe1279f8900/public" width="100%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/ae0f935b-372b-4eb0-09f2-902a1a6a8b00/public" width="100%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> <span style="color:blue">Phenols</span> $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Reimer-tiemann reaction</B></primary></p>
<p></B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/65d0a737-ef6e-45a1-80fb-d3f418076600/public" width="40%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ <span style="color:blue">Reimer-tiemann reaction</span> $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Mechanism of reimer-tiemann reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
</div>
<div style='float: right; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/1480c9e1-acd5-4981-2887-41b319130e00/public" width="40%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/da7c28fb-0221-483f-1a45-6c85badad300/public" width="40%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ <span style="color:blue">Mechanism of reimer-tiemann reaction</span> $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Mechanism of reimer-tiemann reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
</div>
<div style='float: right; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/e1458cbf-98b5-42f3-aae4-d6027a0a3700/public" width="40%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/65b34cf3-311f-4ece-45ea-9052f963f200/public" width="40%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ <span style="color:blue">Mechanism of reimer-tiemann reaction</span> $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Reimer-tiemann reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/e3e67d74-9ef7-4ff4-2fab-37caa8328200/public" width="35%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/7fab823d-cdba-46c9-6d13-263a1d8b1400/public" width="40%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ <span style="color:blue">Reimer-tiemann reaction</span> $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Kolbe’s reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<ul>
<li><strong>It is also known as Kolbe - Schmitt Reaction</strong></li>
</ul>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/43ca0447-e682-4764-6b4c-9b1347141800/public" width="35%" >
</div>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/7fd44579-79bc-424b-bec5-090cc6b70c00/public" width="40%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ <span style="color:blue">Kolbe's reaction</span> $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Oxidation</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<ul>
<li><strong>Oxidation</strong>: High $e^{-}$ density easily get oxidized in air to given pink colour.</li>
</ul>
</div>
<div style='float: left; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/4bd3deb8-01ef-4137-27c7-5aa0e2e20800/public" width="40%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/7df64ea2-9940-4d50-c3f1-9469a99dd700/public" width="50%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ <span style="color:blue">Oxidation</span> $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Gatterman’s aldehyde synthesis</B></primary></p>
<hr>
<main>
<div style='float: left; width:50%;font-size:22px;text-align:left'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/30fbf379-3524-4dcf-c974-62b2a7fcb400/public" width="100%" >
</div>
<div style='float: right; width:50%;font-size:22px;text-align:left'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/3b584939-cfb7-4639-7240-dc0e42cf3800/public" width="100%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ <span style="color:blue">Gatterman's aldehyde synthesis</span> $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Coupling reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<ul>
<li>This is the coupling reaction with diazonium salt (Azodye formation)</li>
</ul>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/7d60b757-23c7-4c5e-be3a-a289373ab000/public" width="80%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ <span style="color:blue">Coupling reaction</span> $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Phthalein test reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<ul>
<li><strong>Phthalein test reaction is a type of condensation reaction</strong></li>
</ul>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/b2cea50f-c8be-4d4f-65d4-5a1cf873d400/public" width="50%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/4c34499d-3405-44a2-4b9a-838ace9dab00/public" width="45%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ <span style="color:blue">Phthalein test reaction</span> $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Liebermann’s nitroso reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<ul>
<li><strong>Liebermann’s nitroso reaction is use to test for phenol</strong></li>
</ul>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/c7c3a5be-a385-4167-3cfc-ba8d09346f00/public" width="45%" >
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/ea3c6986-7074-4485-fd77-583e4c2da300/public" width="40%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ <span style="color:blue">Liebermann's nitroso reaction</span> $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Liebermann’s nitroso reaction</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/63851c86-c078-45ed-5b4c-5ce0d2531200/public" width="60%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ <span style="color:blue">Liebermann's nitroso reaction</span> $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Bakelite</B></primary></p>
<hr>
<main>
<div style='float: left; width:60%;font-size:22px;text-align:left'>
<ul>
<li>
<p>Bakelite is the synthesis of phenol-formaldehyde resin</p>
</li>
<li>
<p>Lederer Manasse</p>
</li>
</ul>
</div>
<div style='float: right; width:40%;'>

<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/09a495d1-90be-475b-d857-04c5e97a6500/public" width="100%" >
</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ <span style="color:blue">Bakelite</span> $\rightarrow$ Fries rearrangement $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Fries rearrangement</B></primary></p>
<hr>
<main>
<div style='float: left; width:50%;font-size:22px;text-align:left'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/678e4c43-c08c-4c8e-22a9-b04488c9dd00/public" width="100%" >
</div>
<div style='float: right; width:50%;font-size:22px;text-align:left'>

<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/2dac40a9-bdd3-436a-2eec-5790c7789400/public" width="100%" >
</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ <span style="color:blue">Fries rearrangement</span> $\rightarrow$ Mechanism of fries rearrangement </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Mechanism of fries rearrangement
</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;font-size:22px;text-align:left'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/ff9d2a85-19bf-4fba-6e9e-d480d0d92a00/public" width="35%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ <span style="color:blue">Mechanism of fries rearrangement</span> </footer>

<p><Success style="float:center;text-align:center;font-size:28px;"> <B>Phenols Lecture-2</B></Success></p>
<p><primary style="float:center;text-align:center;font-size:24px;"> <B>Mechanism of fries rearrangement</B></primary></p>
<hr>
<main>
<div style='float: left; width:100%;'>
<img src="https://imagedelivery.net/YfdZ0yYuJi8R0IouXWrMsA/6c6cd6f3-0911-4da5-310c-3942f5df6e00/public" width="50%" >

</div>
</main>
<hr>
<footer style="font-size:18px;"> Phenols $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Mechanism of reimer-tiemann reaction $\rightarrow$ Reimer-tiemann reaction $\rightarrow$ Kolbe's reaction $\rightarrow$ Oxidation $\rightarrow$ Gatterman's aldehyde synthesis $\rightarrow$ Coupling reaction $\rightarrow$ Phthalein test reaction $\rightarrow$ Liebermann's nitroso reaction $\rightarrow$ Bakelite $\rightarrow$ Fries rearrangement $\rightarrow$ <span style="color:blue">Mechanism of fries rearrangement</span> </footer>