1. When 1- phenyl ethane is oxidized with a strong oxidizing agent like KMnO4, it forms a benzoic acid ion.
2. When phthalic acid is treated with SoCl2 it chlorinates both carboxyl group to form ptthaloyl chloride.
3. When benzaldehyde is treated with semicarbazide to form benzaldehyde semicarbazone.
4. When benzene is mixed with benzoyl chloride in presence of Anhyd.AlCl3 to give benzophenone.
5. When 4-oxocyclohexanecarbeldehyde is treated with tollens reagent it gets oxidized to carboxylate anion as it is aldehyde it reduces tollens reagent.
6. When 2-formyl benzoic acid is treated with NaCN it produces 2-[1-hydroxycyanom
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1. When 1- phenyl ethane is oxidized with a strong oxidizing agent like KMnO4, it forms a benzoic acid ion.
2. When phthalic acid is treated with SoCl2 it chlorinates both carboxyl group to form ptthaloyl chloride.
3. When benzaldehyde is treated with semicarbazide to form benzaldehyde semicarbazone.
4. When benzene is mixed with benzoyl chloride in presence of Anhyd.AlCl3 to give benzophenone.
5. When 4-oxocyclohexanecarbeldehyde is treated with tollens reagent it gets oxidized to carboxylate anion as it is aldehyde it reduces tollens reagent.
6. When 2-formyl benzoic acid is treated with NaCN it produces 2-[1-hydroxycyanomethyl]benzoic acid.
7. When benzaldehyde and propanal mixed equally in presence of Dil.NaOH it forms 2-methyl-3-phenyl-prop-2-enal.
8. When Ethyl 3-oxobutanate is treated with sodium borohydride it converts oxo to hydroxyl.
9. When cyclohexanol is oxidized with CrO3 it forms cyclohexanone.
10. When methylenecyclohexane undergo hydroboration oxidation reaction it will form alcohol. Further treating with oxidizing agent PCC it converts into aldehyde.
When cyclohexylidenecyclohexane undergo ozonolysis it will form cyclohexanone.
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<p><strong>1. </strong>When 1- phenyl ethane is oxidized with a strong oxidizing agent like KMnO<sub>4</sub>, it forms a benzoic acid ion.<br><!-- [if !supportLineBreakNewLine]--></p><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749808997phpGRPSfA.jpeg" alt="" width="567" height="145" loading="lazy"></picture></div><div class="figure"><strong>2. </strong>When phthalic acid is treated with SoCl<sub>2</sub> it chlorinates both carboxyl group to form ptthaloyl chloride.</div><div class="figure"><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809039phpGUIbqc.jpeg" alt="" width="385" height="133" loading="lazy"></picture></div><div class="figure"><strong>3.</strong> When benzaldehyde is treated with semicarbazide to form benzaldehyde semicarbazone.</div><div class="figure"><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809134phpIJ1Z2b.jpeg" alt="" width="717" height="108" loading="lazy"></picture></div><div class="figure"><p><strong>4.</strong> When benzene is mixed with benzoyl chloride in presence of Anhyd.AlCl<sub>3</sub> to give benzophenone.</p><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809202phpBTYe6O.jpeg" alt="" width="633" height="139" loading="lazy"></picture></div><div class="figure"><p><strong>5.</strong> When 4-oxocyclohexanecarbeldehyde is treated with tollens reagent it gets oxidized to carboxylate anion as it is aldehyde it reduces tollens reagent.</p></div></div><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809252phpfIpNDa.jpeg" alt="" width="591" height="126" loading="lazy"></picture></div><div class="figure"><p><strong>6. </strong>When 2-formyl benzoic acid is treated with NaCN it produces 2-[1-hydroxycyanomethyl]benzoic acid.</p></div></div><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809300phpfMQ6cv.jpeg" alt="" width="555" height="192" loading="lazy"></picture></div><div class="figure"><strong>7. </strong>When benzaldehyde and propanal mixed equally in presence of Dil.NaOH it forms 2-methyl-3-phenyl-prop-2-enal.<br><!-- [if !supportLineBreakNewLine]--><br><!--[endif]--></div><div class="figure"><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809335php84Q1QG.jpeg" alt="" width="422" height="147" loading="lazy"></picture></div><div class="figure"><p><strong>8. </strong>When Ethyl 3-oxobutanate is treated with sodium borohydride it converts oxo to hydroxyl.</p><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809386phpje8XPP.jpeg" alt="" width="565" height="118" loading="lazy"></picture></div><div class="figure"><p><strong>9. </strong>When cyclohexanol is oxidized with CrO<sub>3</sub> it forms cyclohexanone.</p></div></div><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809423php0Q36yU.jpeg" alt="" width="403" height="103" loading="lazy"></picture></div><div class="figure"><p><strong>10. </strong>When methylenecyclohexane undergo hydroboration oxidation reaction it will form alcohol. Further treating with oxidizing agent PCC it converts into aldehyde.</p></div></div><div class="photo-widget-full"><div class="figure"><picture><source srcset="" media="(max-width: 500px)"><img src="https://images.shiksha.com/mediadata/images/1749809462php6oVN91.jpeg" alt="" width="409" height="213" loading="lazy"></picture></div><div class="figure"><p>When cyclohexylidenecyclohexane undergo ozonolysis it will form cyclohexanone.</p></div></div></div></div></div></div></div><div class="figure"> </div></div><p> </p></div><div class="figure"> </div></div><p> </p></div></div><p> </p><p><br><!--[endif]--></p>
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2. When phthalic acid is treated with SoCl2 it chlorinates both carboxyl group to form ptthaloyl chloride.
3. When benzaldehyde is treated with semicarbazide to form benzaldehyde semicarbazone.
