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To prepare propan-2-ol from methyl magnesium iodide, the chemical reagent required is:
A.\[C{H_3}CHO\]
B.\[HCHO\]
C.\[C{H_3}COC{H_3}\]
D.\[C{O_2}\]
Answer
402k+ views
Hint: We must have to know that the propan-2-ol, otherwise known as isopropyl alcohol, is a chemical compound having the formula \[{C_3}{H_8}O\]. Here the isopropyl group is attached with a hydroxyl group and there is a formation of secondary alcohol. And the alcohol carbon atom is linked with two different carbon atoms. The propan – 2- ol is mainly used for the preparation of solvents like dye solutions, soap, etc.
Complete answer:
When the acetaldehyde is reacting with methyl magnesium iodide, there is a formation of secondary alcohol which is propan – 2 – ol.
Here the methyl magnesium iodide is linked with carbonyl carbon and there is a formation of adduct. And due to the electronegativity difference, adducts have partial charges. And thus adduct is reacted with water and undergoes the hydrolysis, will get propan – 2 – ol.
Let’s see the reaction,
Hence, option (A) is correct.
When the formaldehyde is reacting with methyl magnesium iodide, (Grignard reagent), there is a formation of primary alcohol. But here, propan -2- ol is a secondary alcohol. Hence, the option (B) is incorrect.
When acetone is reacting with methyl magnesium iodide, there is a formation of 2 -methyl 2 propanol and will not get propan – 2 – ol. Hence, option (C) is incorrect.
When the carbon dioxide is reacting with methyl magnesium bromide, the product should be a carboxylic acid and not give propan – 2 – ol. Hence, the option (D) is incorrect.
Hence, option (A) is correct.
Note:
We need to know that the Grignard reagent is a chemical compound which is widely used as a reagent in organic synthesis. The general formula of Grignard reagent is, \[R - Mg - X\]. If the Grignard reagent is reacted with aldehyde or ketone, there is a formation of secondary alcohol and tertiary alcohol respectively. But, when the formaldehyde is reacting with Grignard reagent, there is a formation of primary alcohol.
Complete answer:
When the acetaldehyde is reacting with methyl magnesium iodide, there is a formation of secondary alcohol which is propan – 2 – ol.
Here the methyl magnesium iodide is linked with carbonyl carbon and there is a formation of adduct. And due to the electronegativity difference, adducts have partial charges. And thus adduct is reacted with water and undergoes the hydrolysis, will get propan – 2 – ol.
Let’s see the reaction,
![seo images](https://www.vedantu.com/question-sets/57dbe58d-cff2-4290-a680-2362951f09872742905675632781948.png)
Hence, option (A) is correct.
When the formaldehyde is reacting with methyl magnesium iodide, (Grignard reagent), there is a formation of primary alcohol. But here, propan -2- ol is a secondary alcohol. Hence, the option (B) is incorrect.
When acetone is reacting with methyl magnesium iodide, there is a formation of 2 -methyl 2 propanol and will not get propan – 2 – ol. Hence, option (C) is incorrect.
When the carbon dioxide is reacting with methyl magnesium bromide, the product should be a carboxylic acid and not give propan – 2 – ol. Hence, the option (D) is incorrect.
Hence, option (A) is correct.
Note:
We need to know that the Grignard reagent is a chemical compound which is widely used as a reagent in organic synthesis. The general formula of Grignard reagent is, \[R - Mg - X\]. If the Grignard reagent is reacted with aldehyde or ketone, there is a formation of secondary alcohol and tertiary alcohol respectively. But, when the formaldehyde is reacting with Grignard reagent, there is a formation of primary alcohol.
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