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1-Phenylethanol can be prepared by the reaction of benzaldehyde with
  • a)
    Methyl bromide
  • b)
    Ethyl iodide and magnesium
  • c)
    Methyl iodide and magnesium
  • d)
    Methyl bromide and aluminium bromide
Correct answer is option 'C'. Can you explain this answer?
Most Upvoted Answer
1-Phenylethanol can be prepared by the reaction of benzaldehyde witha)...
Preparation of 1-Phenylethanol using Benzaldehyde and Methyl Iodide with Magnesium

Introduction:
1-Phenylethanol is an organic compound with the formula C6H5CH2CH2OH. It is also known as α-phenylethanol or benzyl alcohol. This compound is used in various applications, including as a fragrance compound and as a precursor in the synthesis of other organic compounds.

Preparation:
1-Phenylethanol can be prepared by the reaction of benzaldehyde with methyl iodide and magnesium. This reaction is known as the Grignard reaction and is a commonly used method for the synthesis of alcohols.

Procedure:
The reaction proceeds in several steps as follows:

1. Formation of the Grignard reagent:
- Magnesium (Mg) is reacted with methyl iodide (CH3I) in anhydrous ether (diethyl ether) to form a Grignard reagent, which is a magnesium alkyl halide compound.
- The reaction can be represented by the following equation:
Mg + CH3I → MgI(CH3)

2. Addition of the Grignard reagent to benzaldehyde:
- The Grignard reagent, which is a nucleophile, reacts with benzaldehyde (C6H5CHO) in anhydrous ether as the solvent.
- The nucleophilic carbon of the Grignard reagent attacks the electrophilic carbon of the benzaldehyde, resulting in the formation of a new carbon-carbon bond.
- The reaction can be represented by the following equation:
MgI(CH3) + C6H5CHO → C6H5CH2MgI + CH3OH

3. Acid workup:
- The reaction mixture is then treated with a dilute acid, typically hydrochloric acid (HCl), to protonate the alkoxide intermediate and convert it into the desired alcohol.
- The acid workup also helps in the removal of any remaining Grignard reagent and by-products.
- The final step can be represented by the following equation:
C6H5CH2MgI + HCl → C6H5CH2OH + MgClI

Conclusion:
The reaction of benzaldehyde with methyl iodide and magnesium followed by acid workup allows for the synthesis of 1-Phenylethanol. This method is a practical and efficient way to prepare this compound in the laboratory. The Grignard reaction is a versatile tool in organic synthesis and finds wide applications in the preparation of various functional groups.
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1-Phenylethanol can be prepared by the reaction of benzaldehyde witha)...
C
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1-Phenylethanol can be prepared by the reaction of benzaldehyde witha)Methyl bromideb)Ethyl iodide and magnesiumc)Methyl iodide and magnesiumd)Methyl bromide and aluminium bromideCorrect answer is option 'C'. Can you explain this answer?
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1-Phenylethanol can be prepared by the reaction of benzaldehyde witha)Methyl bromideb)Ethyl iodide and magnesiumc)Methyl iodide and magnesiumd)Methyl bromide and aluminium bromideCorrect answer is option 'C'. Can you explain this answer? for JEE 2024 is part of JEE preparation. The Question and answers have been prepared according to the JEE exam syllabus. Information about 1-Phenylethanol can be prepared by the reaction of benzaldehyde witha)Methyl bromideb)Ethyl iodide and magnesiumc)Methyl iodide and magnesiumd)Methyl bromide and aluminium bromideCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for JEE 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for 1-Phenylethanol can be prepared by the reaction of benzaldehyde witha)Methyl bromideb)Ethyl iodide and magnesiumc)Methyl iodide and magnesiumd)Methyl bromide and aluminium bromideCorrect answer is option 'C'. Can you explain this answer?.
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