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Hello everyone.
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Here is a series of reaction from the compound given there.
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So the compound given here is cyclohexanone.
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When this cyclohexanone carries out series of reaction, it has to yield products p1, p2 and p3.
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We have to find out about compound p3 in the sequence.
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So first of all, it has to be treated with n, a, o, and there is ethyl groam.
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So this is plus and this is.
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Minus so we know that in the presence of any o ethyl group in the presence of ch3 c double bond o and o ethyl group so we have to just undergo the carbonyl carbon has to attack the alpha place okay so the product obtained here see there is a hydrogen isn't it so as the hydrogen is alpha hydrogen is eliminated carbon gets the negative charge so we know that carbon carbon is positive so we have to just insert this carbonyl carbon at this place so the product obtained here will be the ring i am not touching oh h here so this is further connected to c double bond o and o ethyl group okay so this is the first product so let me call this as p1 in the sequence now this p1 has to undergo following series of change.
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So first of all, it has to undergo reduction with the lithium aluminum hydride.
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So when it is undergoing the reduction, my ketone is going to become alcohol.
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So i am going to have this to oh...