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Lithium aluminium hydride reduces an ester all the way… | StemPy Lab

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Lithium aluminium hydride reduces an ester all the way to alcohols. How many hydride ions does one ester group take in this reduction?

ChemistryMediumHigh School (11–12)Organic Compounds with Functional Groups › Aldehydes, Ketones and Carboxylic Acids

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Lithium aluminium hydride reduces an ester all the way to alcohols. How many hydride ions does one ester group take in this reduction?

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← Benzaldehyde is heated with ethanoic anhydride and sodium ethanoate. The product after acidification is Which one-step reaction increases the number of carbon atoms of a Grignard reagent by one? →

More onOrganic Compounds with Functional Groups › Aldehydes, Ketones and Carboxylic Acids

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