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What would be the reactant and reagent u...

What would be the reactant and reagent used to obtain 2,4 - dimethylpentan-3-ol ?

A

Propanal and proyl magnesium bromide

B

3-Methybutanal and 2- methyl magnesium iodide

C

2,2-Dimethylpropanone and methyl magnesium iodide

D

2- Methylpropanal and isopropyl magnesium iodide

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The correct Answer is:
To obtain 2,4-dimethylpentan-3-ol, we need to identify the appropriate reactant and reagent. Here’s a step-by-step breakdown of the solution: ### Step 1: Identify the Target Compound The target compound is 2,4-dimethylpentan-3-ol. This indicates that we need a pentane backbone (5 carbon atoms) with two methyl groups on the 2nd and 4th carbon and an alcohol (-OH) group on the 3rd carbon. ### Step 2: Determine the Structure of the Reactant To synthesize this compound, we can start with a suitable ketone or aldehyde that can be converted into the desired alcohol. A good starting point is 2-methylpropan-2-ol, which has a structure that can be modified to yield the target compound. ### Step 3: Select the Grignard Reagent To introduce the required carbon chain and functional group, we can use a Grignard reagent. The Grignard reagent we will use is isopropyl magnesium iodide (C3H7MgI), which will add to the carbonyl compound. ### Step 4: Reaction Mechanism 1. **Formation of the Grignard Reagent**: Isopropyl magnesium iodide is formed from isopropyl bromide and magnesium in dry ether. 2. **Nucleophilic Addition**: The Grignard reagent will act as a nucleophile and attack the carbonyl carbon of the ketone (or aldehyde), leading to the formation of an alkoxide intermediate. 3. **Protonation**: Upon hydrolysis (adding water), the alkoxide will be converted to the corresponding alcohol, yielding 2,4-dimethylpentan-3-ol. ### Step 5: Final Product Confirmation After the reaction, we will confirm that the product formed is indeed 2,4-dimethylpentan-3-ol by checking the structure and ensuring that the methyl groups are on the correct carbon atoms and that the alcohol is on the 3rd carbon. ### Summary of Reactants and Reagents - **Reactant**: 2-methylpropan-2-ol (or a suitable ketone/aldehyde) - **Reagent**: Isopropyl magnesium iodide (C3H7MgI)

To obtain 2,4-dimethylpentan-3-ol, we need to identify the appropriate reactant and reagent. Here’s a step-by-step breakdown of the solution: ### Step 1: Identify the Target Compound The target compound is 2,4-dimethylpentan-3-ol. This indicates that we need a pentane backbone (5 carbon atoms) with two methyl groups on the 2nd and 4th carbon and an alcohol (-OH) group on the 3rd carbon. ### Step 2: Determine the Structure of the Reactant To synthesize this compound, we can start with a suitable ketone or aldehyde that can be converted into the desired alcohol. A good starting point is 2-methylpropan-2-ol, which has a structure that can be modified to yield the target compound. ...
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NCERT FINGERTIPS-ALCOHOLS,PHENOLS AND ETHERS-Alcohols And Phenols
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