Best reagent set to convert an acid chloride into an aldehyde without over-reduction A NaBH₄, alcohol B LiAlH₄, ether C
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Chapter 18: Aldehydes, Carboxylic Acids and Related Compounds (Set-4)
Best reagent for converting an acid chloride to an aldehyde A Hot KMnO₄ B NaBH₄ reduction C Rosenmund reduction D
Continue readingChapter 18: Aldehydes, Carboxylic Acids and Related Compounds (Set-3)
When propanal is treated with Tollens’ reagent, the organic product formed is mainly A Propanoic acid B 1-Propanol C Propanoate
Continue readingChapter 18: Aldehydes, Carboxylic Acids and Related Compounds (Set-2)
Which reagent converts an aldehyde to a primary alcohol under mild conditions A Hot KMnO₄ oxidation B Conc. H₂SO₄ dehydration
Continue readingChapter 18: Aldehydes, Carboxylic Acids and Related Compounds (Set-1)
Which method commonly converts a primary alcohol into an aldehyde under controlled oxidation? A PCC oxidation B KMnO₄, hot C
Continue readingChapter 17: Alcohols, Phenols and Ethers (Set-5)
Acid hydration of 3,3-dimethyl-1-butene can give rearranged alcohol mainly due to A Radical chain transfer B Carbocation rearrangement C Concerted
Continue readingChapter 17: Alcohols, Phenols and Ethers (Set-4)
Hydration of 2-methylpropene under acidic conditions mainly forms which alcohol A Acetone major B Isobutanol major C tert-Butanol major D
Continue readingChapter 17: Alcohols, Phenols and Ethers (Set-3)
Acid-catalyzed hydration of propene mainly forms which alcohol A 1-propanol mainly B Propanal mainly C 2-propanol mainly D Propanone mainly
Continue readingChapter 17: Alcohols, Phenols and Ethers (Set-2)
Which reagent converts an alkene directly into an alcohol by adding water under acidic conditions A SOCl2 reagent B NaBH4
Continue readingChapter 17: Alcohols, Phenols and Ethers (Set-1)
When propene is hydrated under acidic conditions, which functional group is formed in the major organic product? A A. Primary
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