Question
The end product in the below-mentioned reaction is:
Acetone
Methane
Acetaldehyde
Ethyl alcohol
Step 1: Methyl bromide () reacts with to undergo nucleophilic substitution (), yielding methyl cyanide or acetonitrile (Compound A) as the major product. Step 2: Acetonitrile () on complete acidic hydrolysis () gives acetic acid or ethanoic acid (Compound B). Step 3: Acetic acid () is reduced by the strong reducing agent lithium aluminium hydride () in the presence of ether to form ethyl alcohol or ethanol (Compound C). Thus, the final product C is ethyl alcohol.
This question aligns with the NEET CHEMISTRY syllabus, specifically targeting concepts from Alcohols, Phenols and Ethers. Mastering this topic is crucial for scoring well in the upcoming medical entrance examinations. Solving conceptually related problems will help you understand the nuances of these concepts and improve your problem-solving speed.
More Alcohols, Phenols and Ethers Questions
When phenol is treated with CHCl₃ and NaOH, the product formed is:
Which of the following statement is correct for the stability of ions of ethyl alcohol and phenol:
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Which of the following can be used as the halide component for Friedel-Crafts reaction?
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The most reactive compound among the following toward electrophilic aromatic substitution reaction is:
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Among the following four compounds: (a) Phenol (b) Methyl phenol (c) meta-nitrophenol (d) para-nitrophenol The acidity order is:
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