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The 50 pages that link to Hydrogenation, each with the reason it gives.

• HydrogenRelated: Hydrogen’s ability to add across bonds changes oils and many industrial chemicals.

• Saturated fatRelated: Partial hydrogenation can reduce unsaturation while also producing industrial trans fats.

• KetoneRelated: Catalytic hydrogenation can reduce ketones to secondary alcohols.

• Oleic acidRelated: Hydrogenation can convert oleic acid’s double bond into a saturated chain.

• AcetaldehydeRelated: Catalytic hydrogenation reduces acetaldehyde to ethanol.

• Sugar alcoholRelated: Industrial hydrogenation reduces sugar carbonyl groups to make sugar alcohols.

• MentholRelated: Industrial routes make menthol by hydrogenating compounds such as thymol.

• Stearic acidRelated: Industrial processing can convert unsaturated fatty acids in oils toward saturated products, including stearic acid.

• Vegetable oilRelated: It can make liquid oils more solid; partial hydrogenation can create trans fats.

• EtheneRelated: Hydrogen converts ethene into ethane by saturating its double bond.

• HydroformylationRelated: Hydrogenation converts hydroformylation aldehydes into alcohols.

• MargarineRelated: Partial hydrogenation once made margarine firmer, but could create trans fats.

• Polyunsaturated fatty acidRelated: Food processing can reduce unsaturation and alter fat texture and stability.

• ShorteningRelated: It has been used to make liquid oils firmer for baking.

• Sunflower oilRelated: It can harden sunflower oil, though partial hydrogenation produces trans fats.

• CyclohexeneRelated: Hydrogenation converts cyclohexene into cyclohexane by saturating its double bond.

• AnthraquinoneRelated: Hydrogenation reduces anthraquinone derivatives in the industrial hydrogen peroxide cycle.

• Cottonseed oilRelated: It has been used to make cottonseed oil more solid for food products.

• Double bondRelated: Hydrogenation removes a carbon–carbon double bond by adding hydrogen atoms across it.

• Fatty alcoholRelated: Industrial fatty alcohol production can reduce fatty acids or their esters by hydrogenation.

• Saturated compoundRelated: Hydrogenation can convert unsaturated compounds into saturated ones.

• Geoffrey WilkinsonRelated: Wilkinson’s rhodium catalyst provided a selective route for hydrogenating alkenes.

• Peanut butterRelated: Some formulations use hardened oils to reduce separation and keep the spread firm.

• Cinnamic acidRelated: Hydrogenation converts cinnamic acid’s alkene into the saturated chain of hydrocinnamic acid.

• Group 10 elementRelated: Nickel and palladium catalysts enable industrial and laboratory hydrogenation.

• MaltitolRelated: It converts maltose’s carbonyl group into maltitol’s alcohol group.

• Stearyl alcoholRelated: Hydrogenation can convert unsaturated fatty feedstocks into saturated materials used to make fatty alcohols.

• ButyraldehydeRelated: Catalytic hydrogenation converts butyraldehyde's carbonyl group into an alcohol group.

• IsobutyleneRelated: Hydrogenation saturates isobutylene to form the branched alkane isobutane.

• LactitolRelated: This reaction converts lactose’s reactive carbonyl group into lactitol’s sugar alcohol structure.

• Lithium hydrideRelated: LiH can supply hydride in reduction chemistry, though it is not itself a conventional hydrogenation catalyst.

• PropyneRelated: Hydrogen adds across propyne’s triple bond to form alkenes or propane.

• 2-ButyneRelated: Adding hydrogen to 2-butyne can produce an alkene or, with further reduction, an alkane.

• PropionaldehydeRelated: Catalytic hydrogenation is one industrial route from propionaldehyde to 1-propanol.

• 1-ButyneRelated: Hydrogenation can reduce 1-butyne to butene or, with further reduction, butane.

• CycloheptaneRelated: Hydrogenation of cycloheptene produces cycloheptane.

• Open-chain compoundRelated: Hydrogenation can convert unsaturated open-chain compounds into saturated chains.

• Platinum groupRelated: Palladium and other group metals facilitate hydrogen addition in industrial and laboratory reactions.