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How are aldehydes and ketones reduced to alcohols, and what reagents can be used for this reduction?

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Aldehydes are reduced to primary alcohols, and ketones to secondary alcohols, using sodium borohydride (NaBH₄), lithium aluminium hydride (LiAlH₄), or catalytic hydrogenation.

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  1. Aldehydes and ketones can be reduced to alcohols through catalytic or chemical reduction. Catalytic reduction involves using a metal catalyst, typically Raney nickel or platinum, under hydrogen gas (H₂) conditions. Alternatively, chemical reduction involves the use of reducing agents like sodium borohydride (NaBH₄) or lithium aluminum hydride (LiAlH₄). Sodium borohydride is milder and is commonly used for aldehyde and ketone reductions, while lithium aluminum hydride is a stronger reducing agent suitable for a wider range of carbonyl reductions, including those of carboxylic acids and esters. The reactions result in the addition of hydrogen, converting the carbonyl group to an alcohol.

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