In organic chemistry, we are learning multistep synthesis but I am having trouble with it. Please help with this problem.
Answer –
We are given, cyclohexane and from that we need to synthesis of 1-propylcyclohexanol.
First we need to treat this cyclohexane with Cl2 in light and formed chlorocyclohexane by free radical mechanism. When this chlorocyclohexane is reacted with base like NaOH then there is SN2 reaction and formed cyclohexanol. When this cyclohexanol treated with chromic acid in acid there is oxidation and formed cyclohexanone. When this cyclohexanone reacted with Grignard reagent in acid there is formed 1-propylcyclohexanol
Reaction –
In organic chemistry, we are learning multistep synthesis but I am having trouble with it. Please...
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Organic Chemistry Multisynthesis problem can someone please list the reagents and full multistep mechanism for this problem image attached HO
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I am having trouble solving these types of problems. Please help me understand by explaining and showing me the steps and methods needed to work this out. thank you.