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Statements

Subject Item
dbr:Caesium_acetate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Caffeic_aldehyde
gold:hypernym
dbr:Aldehyde
Subject Item
dbr:Calciseptine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Calcium_hypochlorite
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Calostomal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cannizzaro_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Capnellene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Carbohydrate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Carbomethoxymethylenetriphenylphosphorane
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Carbon_monoxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cardiac_glycoside
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Amide_reduction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aminal
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dbr:Aldehyde
Subject Item
dbr:Amine_dehydrogenase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Amine_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Amine_oxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aminoaldehydes_and_aminoketones
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ammoxidation
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dbr:Aldehyde
Subject Item
dbr:Bearded_emperor_tamarin
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dbr:Aldehyde
Subject Item
dbr:Beer_chemistry
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Beer_fault
rdfs:seeAlso
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Subject Item
dbr:Benary_reaction
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Subject Item
dbr:Benedict's_reagent
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Subject Item
dbr:Potassium_cyanide
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dbr:Aldehyde
Subject Item
dbr:Potassium_permanganate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Potassium_peroxymonosulfate
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dbr:Aldehyde
Subject Item
dbr:Prins_reaction
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Subject Item
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Subject Item
dbr:Propane-1,3-dithiol
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Subject Item
dbr:Propiolaldehyde
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Subject Item
dbr:Propionaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Protocatechuic_aldehyde
gold:hypernym
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Subject Item
dbr:Ptaquiloside
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pummerer_rearrangement
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dbr:Aldehyde
Subject Item
dbr:Pyrazole
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Subject Item
dbr:Pyridine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pyridine-4-carbaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pyridinium_chlorochromate
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dbr:Aldehyde
Subject Item
dbr:Pyrrole
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dbr:Aldehyde
Subject Item
dbr:Pyrrolidine
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dbr:Aldehyde
Subject Item
dbr:Quinoline
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Subject Item
dbr:Quinoxaline
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Subject Item
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dbr:Aldehyde
Subject Item
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Subject Item
dbr:Roskamp_reaction
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Subject Item
dbr:Samarium(II)_bromide
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dbr:Aldehyde
Subject Item
dbr:Samarium(II)_iodide
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dbr:Aldehyde
Subject Item
dbr:Sandworm_(Dune)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Sarett_oxidation
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Subject Item
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dbr:Aldehyde
Subject Item
dbr:Schmidt_reaction
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Subject Item
dbr:Schwartz's_reagent
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Subject Item
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Subject Item
dbr:Elastic_fiber
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Electrosynthesis
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Subject Item
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Subject Item
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Subject Item
dbr:Engine
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Subject Item
dbr:Enzyme_inhibitor
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Subject Item
dbr:Epicuticular_wax
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Musth
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Lysyl_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Metal_carbonyl
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dbr:Aldehyde
Subject Item
dbr:Metal–organic_framework
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Methylenation
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Subject Item
dbr:Methylglyoxal_pathway
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dbr:Aldehyde
Subject Item
dbr:Methylglyoxal_synthase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Omega_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:One-pot_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Wood–Ljungdahl_pathway
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Takai_olefination
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Prodiginines
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Sigmatropic_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Corey-Gilman-Ganem_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
dbo:wikiPageRedirects
dbr:Aldehyde
Subject Item
dbr:Baudisch_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Beetle
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Benzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Benzene-1,2-dithiol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Benzylamine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Betti_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Biginelli_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bilane
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Biochemistry
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bis(2-ethylhexyl)_phthalate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bis(trimethylsilyl)sulfide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bischler–Napieralski_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bispidine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Borane_tert-butylamine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Borinic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bourgeonal
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dbr:Aldehyde
gold:hypernym
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Subject Item
dbr:Bouveault_aldehyde_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Decanal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Decarbonylation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Deoxyribose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Dess–Martin_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Dess–Martin_periodinane
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alfred_Wöhlk
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkan-1-ol_dehydrogenase_(acceptor)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkanesulfonate_monooxygenase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkenylglycerophosphocholine_hydrolase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkenylglycerophosphoethanolamine_hydrolase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkoxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkyl_nitrites
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkylimino-de-oxo-bisubstitution
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkyne
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alkynylation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Applejack_(drink)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Apricot
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Horner–Wadsworth–Emmons_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hugo_Schiff
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hydrazine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hydroformylation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hydroxylamine-O-sulfonic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hydroxylammonium_sulfate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hydroxymethylfurfural
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hyoscyamine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hypochlorous_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Johnson–Corey–Chaykovsky_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aldehyde_dehydrogenase_3_family,_member_A1
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Beta-Hydride_elimination
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:List_of_chemical_compounds_with_unusual_names
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lithium_aluminium_hydride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pentanal
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dbr:Aldehyde
gold:hypernym
dbr:Aldehyde
Subject Item
dbr:Pentatomidae
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Perilla_frutescens
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Perillaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Periodic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Perkin_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Permanganate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Peterson_olefination
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Petrenko-Kritschenko_piperidone_synthesis
dbo:wikiPageWikiLink
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Subject Item
dbr:Petroleum
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:OR10J5
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:OR52D1
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Semipinacol_rearrangement
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Prostaglandin_F_synthase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pseudoacid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pseudocalanus_newmani
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Zincke_aldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Α,β-Unsaturated_carbonyl_compound
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:(Chloromethylene)triphenylphosphorane
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:(S)-hydroxynitrile_lyase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:(Trimethylsilyl)methyllithium
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:(Z)-9-Tricosene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:-al
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:-ene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:-ose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1,1,2,2-Tetrachloroethane
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1,3,4-Oxadiazole
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1,3-Bisphosphoglyceric_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1,3-Dipolar_cycloaddition
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1,5-Diazacyclooctane
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1-Hexene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1-Octene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:1-deoxy-D-xylulose-5-phosphate_synthase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Collins_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Composition_of_electronic_cigarette_aerosol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Composition_of_heated_tobacco_product_emissions
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Conia-ene_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Coniine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Corey–Fuchs_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cornforth_reagent
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Criegee_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Anaerobic_digestion
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Anal_gland
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:McMurry_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Meerwein–Ponndorf–Verley_reduction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ruthenium_red
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ruthenium_tetroxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Safety_of_electronic_cigarettes
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Saffron
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Salazinic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Chemical_substance
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ester
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cho
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Geminal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Geminal_diol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Geminal_halide_hydrolysis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Low-density_polyethylene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Norrish_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oak_(wine)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Odor
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Orange_(fruit)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Rive_Gauche_(perfume)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Serine_hydroxymethyltransferase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Structural_isomer
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Unsaturated_hydrocarbon
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oxidation_of_primary_alcohols_to_carboxylic_acids
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pentose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pyranose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pyridoxine_5′-phosphate_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pyrococcus_furiosus
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pyrogallolarenes
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Quinine_total_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Chromic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Chromium(VI)_oxide_peroxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cis-3-Hexen-1-ol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Citronellal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Claisen_rearrangement
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Clathrus_ruber
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Clemmensen_reduction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cobalt_tetracarbonyl_hydride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Colin_Raston
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Electronic_cigarette
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Elias_James_Corey
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Endiandric_acid_C
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Enol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Epimerox
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Friedel–Crafts_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Fukuyama_reduction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Furfural
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Gamma-Hydroxybutyraldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ganem_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Georg_Wittig
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Gertrude_Maud_Robinson
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Gewald_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glossary_of_chemistry_terms
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glucose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glucuronolactone
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glyceraldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glycine_betaine_aldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glycolaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glyoxal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Glyoxylic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Gonyautoxin
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Gossypol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Molybdenum_disulfide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Monoamine_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Monosaccharide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Mucobromic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Muscarine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:N,N'-Dicyclohexylcarbodiimide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:N-Butyllithium
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:N-tert-Butylbenzenesulfinimidoyl_chloride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Concurrent_tandem_catalysis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Congener_(beverages)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Conjugated_microporous_polymer
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Coriander
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Creighton_process
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Criegee_intermediate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Crosslinking_of_DNA
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Thiazole
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Laboratory_flask
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lactarius_deterrimus
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lactol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lactoylglutathione_lyase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Marschalk_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Reducing_sugar
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Organic_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Organic_redox_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Organocopper_compound
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Organomanganese_chemistry
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Organosilicon_compound
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oseltamivir_total_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Otto_Roelen
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ortho_ester
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Angelo_Angeli
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Anomer
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Arabinose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Arpège
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Benzoin_condensation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Benzylic_activation_and_stereocontrol_in_tricarbonyl(arene)chromium_complexes
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bergmann_degradation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Levuglandin
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lilial
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lindgren_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Liquid_smoke
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Luche_reduction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lucifer_yellow
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Luciferase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lupinine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Lyxose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Magic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Malondialdehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Malonic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Malononitrile
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Maltose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Manganese_dioxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Bodroux–Chichibabin_aldehyde_synthesis
dbo:wikiPageWikiLink
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Subject Item
dbr:Chiral_auxiliary
dbo:wikiPageWikiLink
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Subject Item
dbr:Chocolate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Cholesterol_total_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Chondrite
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Strecker_amino_acid_synthesis
dbo:wikiPageWikiLink
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Subject Item
dbr:Sugar
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Delépine_reaction
dbo:wikiPageWikiLink
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Subject Item
dbr:Fatty_aldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
gold:hypernym
dbr:Aldehyde
Subject Item
dbr:Favorskii_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Fehling's_solution
dbo:wikiPageWikiLink
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Subject Item
dbr:Friedrich_Asinger
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Fulvenes
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Functional_group
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hajos–Parrish–Eder–Sauer–Wiechert_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hammick_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Helma_Wennemers
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hemiacetal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Hemithioacetal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Henri_Robert
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ketone
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Krische_allylation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oxo_alcohol
dbo:wikiPageWikiLink
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Subject Item
dbr:Parmesan
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Phenolic_content_in_wine
dbo:wikiPageWikiLink
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Subject Item
dbr:Malate_synthase
dbo:wikiPageWikiLink
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Subject Item
dbr:Sterilization_(microbiology)
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Subject Item
dbr:Stink_bomb
dbo:wikiPageWikiLink
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Subject Item
dbr:Strecker_degradation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Sweetness
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Subject Item
dbr:Tanning_(leather)
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dbr:Aldehyde
Subject Item
dbr:Taste
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Transketolase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Marcel_Delépine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:McFadyen–Stevens_reaction
dbo:wikiPageWikiLink
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Subject Item
dbr:Meyers_synthesis
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Michael_reaction
dbo:wikiPageWikiLink
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Subject Item
dbr:Microfluidics
dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Zoophily
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Subject Item
dbr:Musgraveia_sulciventris
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Subject Item
dbr:Non-methane_volatile_organic_compound
dbo:wikiPageWikiLink
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Subject Item
dbr:2,4-Dinitroaniline
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:2,4-Dinitrophenylhydrazine
dbo:wikiPageWikiLink
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Subject Item
dbr:2-Carboxybenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:2-Chloro-6-fluorotoluene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:2-Iodoxybenzoic_acid
dbo:wikiPageWikiLink
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Subject Item
dbr:2-Mercaptoethanol
dbo:wikiPageWikiLink
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Subject Item
dbr:2-Methylundecanal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:2-Nonenal
dbo:wikiPageWikiLink
dbr:Aldehyde
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dbr:Aldehyde
Subject Item
dbr:2-Propylheptanol
dbo:wikiPageWikiLink
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Subject Item
dbr:Avobenzone
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Butyraldehyde
dbo:wikiPageWikiLink
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Subject Item
dbr:Bürgi–Dunitz_angle
dbo:wikiPageWikiLink
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Subject Item
dbr:Acyl_group
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Threose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Tin(II)_chloride
dbo:wikiPageWikiLink
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Subject Item
dbr:Titanium_tetrachloride
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Trehalose
dbo:wikiPageWikiLink
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Subject Item
dbr:Tributylphosphine
dbo:wikiPageWikiLink
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Subject Item
dbr:Tricresyl_phosphate
dbo:wikiPageWikiLink
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Subject Item
dbr:Trimethylamine_N-oxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Trimethylsilyl_chloride
dbo:wikiPageWikiLink
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Subject Item
dbr:Trimethylsilyl_cyanide
dbo:wikiPageWikiLink
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Subject Item
dbr:Vy_Maria_Dong
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Subject Item
dbr:Vyacheslav_Tishchenko
dbo:wikiPageWikiLink
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Subject Item
dbr:Walter_Reppe
dbo:wikiPageWikiLink
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Subject Item
dbr:Weinreb_ketone_synthesis
dbo:wikiPageWikiLink
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Subject Item
dbr:Wilhelm_Rudolph_Fittig
dbo:wikiPageWikiLink
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Subject Item
dbr:Wilkinson's_catalyst
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Dithiol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Doebner_reaction
dbo:wikiPageWikiLink
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Subject Item
dbr:Droplet-based_microfluidics
dbo:wikiPageWikiLink
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Subject Item
dbr:Drug_metabolism
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Fétizon_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Galactose_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Galantamine_total_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Galium_aparine
dbo:wikiPageWikiLink
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Subject Item
dbr:Corey–Gilman–Ganem_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
dbo:wikiPageRedirects
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Heliconius_charithonia
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ionic_liquid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Japp–Maitland_condensation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Laundry_detergent
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Leachate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Linear_alpha_olefin
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Locant
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Long-chain_acyl-(acyl-carrier-protein)_reductase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Orange_oil
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Nitrile_reduction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Nitroalkane_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Pinacol_coupling_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Willey_Glover_Denis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:3,3,4,4-Tetramethyltetrahydrofuran
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:3,4,5-Trimethoxybenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:3-Benzoxepin
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:3-Hydroxyisonicotinaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:3-Nitrobenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:4-Carboxybenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:4-Hydroxynonenal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:4-Methylbenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
gold:hypernym
dbr:Aldehyde
Subject Item
dbr:4-Nitrobenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:5-Hydroxy-2(5H)-furanone
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:6-APB
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:ALC-0315
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Acetal
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Acetaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Acetic_anhydride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Acetylene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aconitine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Acrolein
dbo:wikiPageWikiLink
dbr:Aldehyde
gold:hypernym
dbr:Aldehyde
Subject Item
dbr:Adephaga
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alanine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alcohol_(chemistry)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alcohols_(medicine)
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aldehyde_oxidase
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
n39:b_hammerhead_domain
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
dbo:wikiPageRedirects
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Aliivibrio_fischeri
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Aluminium_borohydride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aluminium_chloride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aluminium_hydride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Aluminium_triethoxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Amide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Amine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ammonium_cyanide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ammonium_dichromate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:D-Galacturonic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Dakin_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Darzens_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alpha-Haloketone
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alpha-ketol_rearrangement
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alpha-olefin
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Alpha_hydroxy_acid
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Subject Item
dbr:Ernst_Otto_Beckmann
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Erythrose
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ethane-1,2-dithiol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ethanol
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ethyl_methylphenylglycidate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ethylenediamine
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ethylvanillin
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ferrocene
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Fischer_indole_synthesis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Flavin_adenine_dinucleotide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Fleming–Tamao_oxidation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Flippin–Lodge_angle
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Formaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Formaldoxime
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Formic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Formyl_cyanide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Angeli–Rimini_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Banert_cascade
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Brook_rearrangement
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Nirmatrelvir
dbo:wikiPageWikiLink
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Subject Item
dbr:Nitro_compound
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Subject Item
dbr:Nitromethane
dbo:wikiPageWikiLink
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Subject Item
dbr:Nitrophenyl_pentadienal
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
gold:hypernym
dbr:Aldehyde
Subject Item
dbr:Nonribosomal_peptide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Nozaki–Hiyama–Kishi_reaction
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Osmium_tetroxide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oxalyl_chloride
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oxazoline
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Oxidized_cellulose
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dbr:Aldehyde
Subject Item
dbr:Oxo-Diels–Alder_reaction
dbo:wikiPageWikiLink
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Subject Item
dbr:Oxygen
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ozone
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ozonide
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Ozonolysis
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:P-Toluenesulfonic_acid
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:PR_toxin
dbo:wikiPageWikiLink
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Subject Item
dbr:Palladium(II)_acetate
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Subject Item
dbr:Palladium(II)_chloride
dbo:wikiPageWikiLink
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Subject Item
dbr:Para-Dimethylaminobenzaldehyde
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Passerini_reaction
dbo:wikiPageWikiLink
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Subject Item
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Subject Item
dbr:Carbohydrate_dehydrogenase
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Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Carbonyl_group
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Subject Item
dbr:Carbonyl_reduction
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Subject Item
dbr:Carbonylation
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Carboxylate_reductase
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Subject Item
dbr:Carboxylic_acid
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Subject Item
dbr:Carcerand
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Subject Item
dbr:Carcinogen
dbo:wikiPageWikiLink
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Subject Item
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dbr:Aldehyde
Subject Item
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Subject Item
dbr:Dialdose
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Subject Item
dbr:Diarylquinoline
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Subject Item
dbr:Dicarbonyl
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Subject Item
dbr:Diesel_exhaust
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Formyl
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dbo:wikiPageRedirects
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Subject Item
dbr:Formylation
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Glycol_cleavage
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Lemieux–Johnson_oxidation
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:ALD
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Iodine_compounds
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Subject Item
dbr:Iron(II)_phthalocyanine
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Subject Item
dbr:Iron(III)_nitrate
dbo:wikiPageWikiLink
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Subject Item
dbr:Isobutyraldehyde
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Subject Item
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Subject Item
dbr:Isoprene
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Subject Item
dbr:Isoquinoline
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Subject Item
dbr:Isovaleraldehyde
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Subject Item
dbr:Isovanillin
gold:hypernym
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Subject Item
dbr:Ivar_Karl_Ugi
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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アルデヒド Aldehid Aldehyde Aldehydy Альдегіди 알데하이드 Aldehido Aldehído Aldehyde Alkanal Aldeído Aldehyde Αλδεΰδες Aldeidi Aildéad Aldehyd ألدهيد Альдегиды Aldehydy Aldehido Aldéhyde
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醛(quán)(英語:aldehyde)是含有甲醯基的一類有機化合物。這種官能團具有結構通式:R-CHO,其中的羰基中心連接了一個氫原子與一個R基團。不帶有R的基團稱為醛基或甲醯基。醛與酮化合物的區别在於羰基所處的位置是在碳鏈骨架的末端或是在兩個碳原子之間。醛在有機化學中很常見,許多的香水都屬醛類。 In organic chemistry, an aldehyde (/ˈældɪhaɪd/) is an organic compound containing a functional group with the structure R−CH=O. The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group. Aldehydes are common and play important roles in the technology and biological spheres. 알데하이드(영어: aldehyde 앨더하이드[*] /ˈædəhˌaid/) 또는 알데히드(독일어: aldehyde)는 탄화수소기에 가 첨가된 화학물질의 총칭이다. 분자식은 RCHO이다. 알코올의 불충분한 산화에 의하여 생기며 자극적인 냄새가 나고 포르밀기의 특성상 산화되기 쉬워 은거울반응이나 펠링반응을 일으키며, 산화한 후에는 카르복시산이 된다. 환원제·향료·마취제 등에 쓰인다. Aldehydy (łac. alcohol dehydrogenatus = „alkohol odwodorniony”) – klasa organicznych związków chemicznych posiadających grupę aldehydową, czyli grupę karbonylową (C−O) połączoną z jednym (−CHO) lub dwoma (CH2O) atomami wodoru. Proste aldehydy, będące pochodnymi alkanów i zawierające w cząsteczce jedną grupę aldehydową to alkanale o wzorze ogólnym CnH2n+1CHO. الألدهيدات هي صنف من المركبات العضوية التي تحوي مجموعة وظيفية كربونيلية وهي مجموعة فعالة لها دور كبير في التفاعلات الكيميائية، فتكون الصيغة العامة للألدهيدات R-CHO، وبهذا يتميز عن الكيتونات التي تحوي بديلين. ويمثل R في الصيغة ذرة هيدروجين أو جذراً ألكيلياً وإذا أزلنا R من الصيغة العامة للألديهايد فإننا نحصل على مجموعة الفورميل (بالإنجليزية: formyl group)‏. تتم تسمية الالديهايدات الاليفاتيه حسب نظام الايوباك كما يأتي : 1_ يتم تحديد اسم أطول سلسلة كاربونية متصلة (مستمرة) تحتوي على مجموعة ألديهايد. Альдегі́ди — аліфатичні та ароматичні органічні хімічні сполуки, що містять альдегідну групу -COH. Альдегіди та кетони характеризуються тим, що містять однакову функціональну групу, яку називають карбонільною або оксигрупою. Альдегіди та кетони відрізняються за характером атомів, що оточують карбонільну групу: у альдегідів хоча б один з валентностей Карбону карбонільної групи витрачається на зв'язок з Гідрогеном. У кетонів обидві валентності карбонільної групи витрачаються на зв'язок з вуглеводневими залишками. Alkanal merujuk pada segolongan senyawa organik yang memiliki fungsional karbonil yang terikat pada rantai karbon di satu sisi dan atom hidrogen di sisi yang lain. Golongan ini dikenal pula sebagai golongan aldehida (aldehida juga merupakan nama gugus fungsional). Contoh senyawa yang paling dikenal dari golongan ini adalah metanal atau lebih populer dengan nama trivialnya formaldehida atau formalin. Aldehydy jsou organické sloučeniny, které obsahují aldehydickou funkční skupinu (-CHO) (pozor na záměnu s alkoholy -COH) na konci uhlovodíkového řetězce. Řadí se mezi karbonylové sloučeniny (spolu s ketony, které obsahují karbonylovou skupinu C=O uvnitř řetězce). Jak aldehydy tak ketony jsou v přírodě velmi běžné. Jde o vonné součásti rostlinných silic a také biochemických reakcí například glykolýzy. Využívají se v průmyslovém měřítku pro organické syntézy uhlíkatých skeletů. Un aldehid és un compost orgànic que conté un grup carbonil terminal, o sigui que el grup carbonil està enllaçat a un àtom d'hidrogen i a un altre àtom de carboni. La fórmula general que representa els compostos que presenten aquest grup funcional és R-CHO. El grup aldehid és electròfil a causa de la deficiència electrònica de l'àtom de carboni. Com en els altres grups funcionals que presenten un grup carbonil, els àtoms d'hidrogen situats en posició α són relativament àcids (en els aldehids pKa ~17) a causa de l'estabilització per ressonància de la base conjugada. Comhdhúile orgánacha iad na haildéid ina bhfuil an grúpa carbóinile −C(H)=O i gceann an tslabhra d'adaimh charbóin. Ó tá dhá nasc oscailte ag an ngrúpa carbóinile, ní mór ceann acu a dhúnadh le hadamh hidrigine H agus an ceann eile ceangailte den tslabhra. Mar sin, is féidir a rá gurb é (nó ) feidhmghrúpa na n-aildéad. Is iad an formaildéad nó an agus an t-aicéataildéad nó an t-eatánal an dá aildéad is simplí. (Mar is léir ón dá shampla seo, is é -ánal is deireadh d'ainmneacha córasacha na n-aildéad, ach bíonn ainmneacha traidisiúnta ar chuid mhór acu agus iad níos coitianta sa litríocht cheimiceach féin ná na hainmneacha córasacha.) Aldehido edo alkanal bat formilo talde bat duen konposatu organiko bat da. Formilo taldea talde funtzional bat da, R-CHO egiturarekin, karbonilo bat zentroan (karbono atomo bat lotura bikoitzarekin oxigeno atomo batekin) hidrogeno bati lotua eta batekin alboan. R talde hori edozein alkilo izan daiteke. R gabeko taldeari aldehido taldea edo formilo taldea izena ematen zaio. Aldehidoak zetonen ezberdinak dira, karboniloa bukaeran jartzen delako, eta ez bi karbono atomoen artean. Aldehidoak oso ohikoak dira kimika organikoan. Aldehido estas organika, alifata kemia kombinaĵo, en kiu la karbonilgrupo (C=O) ligiĝas al la ĉenfina karbonatomo, tio diferencigas de la ketonoj. La ĉenfina karbonila grupo estas tre reakciema. Pro tio aldehidoj tre taŭgas kiel bazmaterialoj por la sintezo de aliaj organikaj kombinaĵoj. La apuda bildo montras la ĝeneralan strukturan formulon de la aldehidoj; R en la plej simpla molekulo (formaldehido) estas H-atomo, cetere iu karbonhidrogeno. La aldehidoj estas sintezeblaj per oksidigo el alkoholoj. La aldehido sen R formas la aldehidan grupon. Aldehyde (aus neulateinisch alcoholus dehydrogenatus, „dehydrierter Alkohol“ oder „Alkohol, dem Wasserstoff entzogen wurde“) sind chemische Verbindungen mit der funktionellen Gruppe –CHO, die Aldehydgruppe oder auch Formylgruppe genannt wird. Die Carbonylgruppe der Aldehyde trägt im Unterschied zu den Ketonen einen Wasserstoff- und einen Kohlenstoffsubstituenten. Eine Ausnahme bildet der einfachste Aldehyd Methanal (Formaldehyd), der zwei Wasserstoffsubstituenten trägt. Aldehyde mit einem Alkylrest (also Alkan-Derivate) werden als Alkanale bezeichnet; deren homologe Reihe leitet sich nomenklatorisch entsprechend von der homologen Reihe der Alkane ab. Weiter existieren Mehrfachaldehyde – wie beispielsweise das Glyoxal, der einfachste Dialdehyd. アルデヒド (aldehyde) とは、分子内に、カルボニル炭素に水素原子が一つ置換した構造を有する有機化合物の総称である。カルボニル基とその炭素原子に結合した水素原子および任意の基(-R)から構成されるため、一般式は R-CHO で表される。任意の基(-R)を取り除いた部分をホルミル基(formyl group)、またはアルデヒド基という。アルデヒドとケトンとでは、前者は炭素骨格の終端となるが、ケトンは炭素骨格の中間点となる点で異なる。多くのアルデヒドは特有の臭気を持つ。 Οι αλδεΰδες είναι ένα υποσύνολο των οξυγονούχων οργανικών ενώσεων, που περιέχουν ως κύρια χαρακτηριστική ομάδα, μια τουλάχιστον «φορμυλομάδα» ή «αλδεϋδομάδα» (-CHO). Η φορμυλομάδα αποτελείται από ένα «καρβονύλιο» (C=O, δηλαδή άτομο άνθρακα συνδεμένο με διπλό δεσμό με ένα άτομο οξυγόνου) και ένα άτομο υδρογόνου. Ο γενικός τους τύπος είναι, λοιπόν, RCHO, όπου R μονοσθενής ανθρακούχα ομάδα (που κανονικά όμως δεν πρέπει περιέχει «ανώτερες» από το φορμύλιο χαρακτηριστικές ομάδες) ή υδρογόνο. Альдеги́ды (от лат. alcohol dehydrogenatus — спирт, лишённый водорода) — класс органических соединений, содержащих альдегидную группу (-CHO). ИЮПАК определяет альдегиды как вещества вида R-CHO, в которых карбонильная группа связана с одним атомом водорода и одной группой R. Un aldéhyde est un composé organique, faisant partie de la famille des composés carbonylés, dont l'un des atomes de carbone primaire (relié au plus à 1 atome de carbone) de la chaîne carbonée porte un groupement carbonyle. Un aldéhyde contient donc la séquence : (R représente une chaîne carbonée.) L'aldéhyde le plus simple (R réduit au seul atome H) est le formaldéhyde (ou méthanal), aussi appelé formol lorsqu'il est en solution aqueuse : Een aldehyde (ook wel alkanal) is: * een functionele groep, bestaande uit een carbonylgroep waaraan een waterstofatoom is gebonden. * een organische chemische verbinding met zo'n groep. Een aldehyde kan worden gemaakt door een primaire alcohol selectief te oxideren. Het eenvoudigste aldehyde is formaldehyde (H2C=O), dat in de vorm van een verdunde oplossing (formaline) als ontsmettings- en conserveringsmiddel wordt gebruikt (sterk water). Andere aldehyden zijn onder andere * Aceetaldehyde (ethanal, CH3-CHO) * Propanal * Butanal * Isobutyraldehyde (isobutanal) Le aldeidi sono composti organici di formula bruta CnH2nO che recano nella loro struttura il gruppo funzionale formile, indicato con -CHO. Il loro nome deriva da "alcol deidrogenato", che è una delle possibili modalità di preparazione. In natura vengono prodotte nei processi di fermentazione degli zuccheri. L'atomo di carbonio legato all'atomo di ossigeno ha ibridazione sp2, questo fa sì che sia al centro di un triangolo grossomodo equilatero sul cui piano giacciono l'ossigeno, l'idrogeno e l'atomo direttamente legato al gruppo carbonile. Los aldehídos son compuestos orgánicos caracterizados por poseer el grupo funcional -CHO (carbonilo).​ Un grupo carbonilo es el que se obtiene separando un átomo de hidrógeno del formaldehído. Como tal no tiene existencia libre, aunque puede considerarse que todos los aldehídos poseen un grupo terminal carbonilo. Los aldehídos se denominan como los alcoholes correspondientes, cambiando la terminación -ol por -al.​ Etimológicamente, la palabra aldehído proviene del latín científico alcohol dehydrogarium (alcohol deshidrogenado).​ En aldehyd är en organisk förening som innehåller en aldehydgrupp (även kallad formylgrupp). Denna grupp består av en kolatom med dubbelbindning till en syreatom och en väteatom. Gruppen betecknas vanligen -CHO. Den liknar, men är inte samma som ,-OH, som är en alkoholgrupp. Aldehyder bildas när primära alkoholer (försiktigt) oxideras, men oxideras oftast själva vidare till motsvarande karboxylsyra. Närbesläktade till aldehyderna är ketonerna, som bildas då sekundära alkoholer oxideras.Oxidation av tertiära alkoholer kan inte uppstå utan att kolskelettet avspjälkas. Em química, aldeído é uma função orgânica que se caracteriza pela presença em sua estrutura do grupamento carbonila (C=O) na extremidade da cadeia, caracterizando a presença de um grupo -CHO na extremidade do composto orgânico, denominado aldoxila, metanoila ou formila.
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Aldehido estas organika, alifata kemia kombinaĵo, en kiu la karbonilgrupo (C=O) ligiĝas al la ĉenfina karbonatomo, tio diferencigas de la ketonoj. La ĉenfina karbonila grupo estas tre reakciema. Pro tio aldehidoj tre taŭgas kiel bazmaterialoj por la sintezo de aliaj organikaj kombinaĵoj. La apuda bildo montras la ĝeneralan strukturan formulon de la aldehidoj; R en la plej simpla molekulo (formaldehido) estas H-atomo, cetere iu karbonhidrogeno. La aldehidoj estas sintezeblaj per oksidigo el alkoholoj. La aldehido sen R formas la aldehidan grupon. Em química, aldeído é uma função orgânica que se caracteriza pela presença em sua estrutura do grupamento carbonila (C=O) na extremidade da cadeia, caracterizando a presença de um grupo -CHO na extremidade do composto orgânico, denominado aldoxila, metanoila ou formila. Aldehyde (aus neulateinisch alcoholus dehydrogenatus, „dehydrierter Alkohol“ oder „Alkohol, dem Wasserstoff entzogen wurde“) sind chemische Verbindungen mit der funktionellen Gruppe –CHO, die Aldehydgruppe oder auch Formylgruppe genannt wird. Die Carbonylgruppe der Aldehyde trägt im Unterschied zu den Ketonen einen Wasserstoff- und einen Kohlenstoffsubstituenten. Eine Ausnahme bildet der einfachste Aldehyd Methanal (Formaldehyd), der zwei Wasserstoffsubstituenten trägt. Aldehyde mit einem Alkylrest (also Alkan-Derivate) werden als Alkanale bezeichnet; deren homologe Reihe leitet sich nomenklatorisch entsprechend von der homologen Reihe der Alkane ab. Weiter existieren Mehrfachaldehyde – wie beispielsweise das Glyoxal, der einfachste Dialdehyd. Альдегі́ди — аліфатичні та ароматичні органічні хімічні сполуки, що містять альдегідну групу -COH. Альдегіди та кетони характеризуються тим, що містять однакову функціональну групу, яку називають карбонільною або оксигрупою. Альдегіди та кетони відрізняються за характером атомів, що оточують карбонільну групу: у альдегідів хоча б один з валентностей Карбону карбонільної групи витрачається на зв'язок з Гідрогеном. У кетонів обидві валентності карбонільної групи витрачаються на зв'язок з вуглеводневими залишками. Alkanal merujuk pada segolongan senyawa organik yang memiliki fungsional karbonil yang terikat pada rantai karbon di satu sisi dan atom hidrogen di sisi yang lain. Golongan ini dikenal pula sebagai golongan aldehida (aldehida juga merupakan nama gugus fungsional). Contoh senyawa yang paling dikenal dari golongan ini adalah metanal atau lebih populer dengan nama trivialnya formaldehida atau formalin. In organic chemistry, an aldehyde (/ˈældɪhaɪd/) is an organic compound containing a functional group with the structure R−CH=O. The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group. Aldehydes are common and play important roles in the technology and biological spheres. Un aldéhyde est un composé organique, faisant partie de la famille des composés carbonylés, dont l'un des atomes de carbone primaire (relié au plus à 1 atome de carbone) de la chaîne carbonée porte un groupement carbonyle. Un aldéhyde contient donc la séquence : (R représente une chaîne carbonée.) L'aldéhyde le plus simple (R réduit au seul atome H) est le formaldéhyde (ou méthanal), aussi appelé formol lorsqu'il est en solution aqueuse : Un aldéhyde dérive formellement d'un alcool primaire (oxydation) dont le groupement hydroxyde -OH est en bout de chaîne et se forme à la suite de l'enlèvement de deux atomes H d'où le nom « alcool déshydrogéné » ou aldéhyde. 醛(quán)(英語:aldehyde)是含有甲醯基的一類有機化合物。這種官能團具有結構通式:R-CHO,其中的羰基中心連接了一個氫原子與一個R基團。不帶有R的基團稱為醛基或甲醯基。醛與酮化合物的區别在於羰基所處的位置是在碳鏈骨架的末端或是在兩個碳原子之間。醛在有機化學中很常見,許多的香水都屬醛類。 Aldehido edo alkanal bat formilo talde bat duen konposatu organiko bat da. Formilo taldea talde funtzional bat da, R-CHO egiturarekin, karbonilo bat zentroan (karbono atomo bat lotura bikoitzarekin oxigeno atomo batekin) hidrogeno bati lotua eta batekin alboan. R talde hori edozein alkilo izan daiteke. R gabeko taldeari aldehido taldea edo formilo taldea izena ematen zaio. Aldehidoak zetonen ezberdinak dira, karboniloa bukaeran jartzen delako, eta ez bi karbono atomoen artean. Aldehidoak oso ohikoak dira kimika organikoan. Aldehidorik sinpleena R-ren lekuan hidrogeno atomoa duen formaldehidoa da. Een aldehyde (ook wel alkanal) is: * een functionele groep, bestaande uit een carbonylgroep waaraan een waterstofatoom is gebonden. * een organische chemische verbinding met zo'n groep. Een aldehyde kan worden gemaakt door een primaire alcohol selectief te oxideren. Het eenvoudigste aldehyde is formaldehyde (H2C=O), dat in de vorm van een verdunde oplossing (formaline) als ontsmettings- en conserveringsmiddel wordt gebruikt (sterk water). Andere aldehyden zijn onder andere * Aceetaldehyde (ethanal, CH3-CHO) * Propanal * Butanal * Isobutyraldehyde (isobutanal) De naamgeving van de aldehyden met 3 of meer koolstofatomen wordt als volgt gedefinieerd:naam alkaan (alkeen, alkyn) + 'al'.Voorbeeld: * propaan → propanal * propeen → propenal * butaan → butanal * but-2-een → but-2-en-1-al * but-2-yn → but-2-yn-1-al Aldehydy jsou organické sloučeniny, které obsahují aldehydickou funkční skupinu (-CHO) (pozor na záměnu s alkoholy -COH) na konci uhlovodíkového řetězce. Řadí se mezi karbonylové sloučeniny (spolu s ketony, které obsahují karbonylovou skupinu C=O uvnitř řetězce). Jak aldehydy tak ketony jsou v přírodě velmi běžné. Jde o vonné součásti rostlinných silic a také biochemických reakcí například glykolýzy. Využívají se v průmyslovém měřítku pro organické syntézy uhlíkatých skeletů. Los aldehídos son compuestos orgánicos caracterizados por poseer el grupo funcional -CHO (carbonilo).​ Un grupo carbonilo es el que se obtiene separando un átomo de hidrógeno del formaldehído. Como tal no tiene existencia libre, aunque puede considerarse que todos los aldehídos poseen un grupo terminal carbonilo. Los aldehídos se denominan como los alcoholes correspondientes, cambiando la terminación -ol por -al.​ Etimológicamente, la palabra aldehído proviene del latín científico alcohol dehydrogarium (alcohol deshidrogenado).​ Οι αλδεΰδες είναι ένα υποσύνολο των οξυγονούχων οργανικών ενώσεων, που περιέχουν ως κύρια χαρακτηριστική ομάδα, μια τουλάχιστον «φορμυλομάδα» ή «αλδεϋδομάδα» (-CHO). Η φορμυλομάδα αποτελείται από ένα «καρβονύλιο» (C=O, δηλαδή άτομο άνθρακα συνδεμένο με διπλό δεσμό με ένα άτομο οξυγόνου) και ένα άτομο υδρογόνου. Ο γενικός τους τύπος είναι, λοιπόν, RCHO, όπου R μονοσθενής ανθρακούχα ομάδα (που κανονικά όμως δεν πρέπει περιέχει «ανώτερες» από το φορμύλιο χαρακτηριστικές ομάδες) ή υδρογόνο. Ως χαρακτηριστική ομάδα, η φορμυλομάδα έπεται, ως προς το χαρακτηρισμό «κύρια χαρακτηριστική ομάδα», του με τύπο [(-COOH) και άλλων όξινων ομάδων, όπως για παράδειγμα της (-SO3H) (καθώς και των παραγώγων τους όπως εστέρες, άλατα, αμίδια και αλογονίδια)] καθώς και κυανομάδας (-C≡Ν) των νιτριλίων, της [(-Ν=C:) καθώς επίσης και ανάλογων ομάδων με φωσφόρο, αρσενικό και αντιμόνιο]. Προηγείται, όμως, όλων των υπόλοιπων χαρακτηριστικών ομάδων. Οι ενώσεις που περιέχουν αλδεϋδομάδες ως δευτερεύουσες χαρακτηριστικές ομάδες έχουν ορισμένες ιδιότητες των αλδεϋδών και ενίοτε συγκατατάσσονται στις αλδεΰδες, από ορισμένους συγγραφείς. Οι αλδεΰδες διαφέρουν, λοιπόν, από τις κετόνες ακριβώς στην παρουσία ενός ατόμου υδρογόνου, συνδεομένου με το καρβονύλιό τους. Στις αλδεΰδες ένα (1) καρβονύλιο βρίσκεται αναγκαστικά στο τέλος της κύριας ανθρακικής αλυσίδας της ένωσης. Οι αλδεΰδες, αν και είναι περισσότερο δραστικές, έχουν παραπλήσιες χημικές ιδιότητες με τις κετόνες με ενδιαφέρουσες και ποικίλες χρήσεις στη βιομηχανία, αποτελώντας χημικά ενδιάμεσα που με διάφορες χημικές αντιδράσεις μετατρέπονται σε άλλες ενώσεις, χρήσιμες στη παραγωγή διαφόρων προϊόντων όπως αρωμάτων, πλαστικών, απορρυπαντικών και φαρμακευτικών προϊόντων. Επίσης, πολλές βιοχημικές ενώσεις περιέχουν αλδεϋδικές ομάδες (ομάδες αλδεϋδών), όπως τα σάκχαρα (συγκεκριμένα οι αλδόζες) και κάποιες στεροειδείς ορμόνες. Альдеги́ды (от лат. alcohol dehydrogenatus — спирт, лишённый водорода) — класс органических соединений, содержащих альдегидную группу (-CHO). ИЮПАК определяет альдегиды как вещества вида R-CHO, в которых карбонильная группа связана с одним атомом водорода и одной группой R. Le aldeidi sono composti organici di formula bruta CnH2nO che recano nella loro struttura il gruppo funzionale formile, indicato con -CHO. Il loro nome deriva da "alcol deidrogenato", che è una delle possibili modalità di preparazione. In natura vengono prodotte nei processi di fermentazione degli zuccheri. Il gruppo funzionale bivalente C=O viene detto carbonile (o "gruppo carbonilico") ed è comune ad aldeidi (R-CHO) e chetoni R-CO-R', dove R o R' sono gruppi alchilici o arilici. Nelle aldeidi il carbonile è legato ad almeno un atomo di idrogeno e ad un radicale alchilico o arilico. Nella formaldeide, che è la prima rappresentante e quindi l'aldeide più semplice è legato a due atomi di idrogeno. Questo fa sì che essa si differenzi da tutte le altre per alcune proprietà: la mancanza di un idrogeno in alfa al carbonile toglie ogni canale di reazione legato all'enolizzazione; la facile ossidabilità fino a CO2, mentre le altre si fermano allo stadio dell'acido carbossilico corrispondente R-COOH, per ossidazione in condizioni non spinte; il carattere maggiormente elettrofilo del suo carbonile. L'atomo di carbonio legato all'atomo di ossigeno ha ibridazione sp2, questo fa sì che sia al centro di un triangolo grossomodo equilatero sul cui piano giacciono l'ossigeno, l'idrogeno e l'atomo direttamente legato al gruppo carbonile. Il composto più semplice della serie è il metanale, o formaldeide, (HCHO) che viene usata come mezzo di conservazione e come battericida. Per le tipiche reazioni delle aldeidi, vedi la voce reazioni di aldeidi e chetoni. アルデヒド (aldehyde) とは、分子内に、カルボニル炭素に水素原子が一つ置換した構造を有する有機化合物の総称である。カルボニル基とその炭素原子に結合した水素原子および任意の基(-R)から構成されるため、一般式は R-CHO で表される。任意の基(-R)を取り除いた部分をホルミル基(formyl group)、またはアルデヒド基という。アルデヒドとケトンとでは、前者は炭素骨格の終端となるが、ケトンは炭素骨格の中間点となる点で異なる。多くのアルデヒドは特有の臭気を持つ。 Un aldehid és un compost orgànic que conté un grup carbonil terminal, o sigui que el grup carbonil està enllaçat a un àtom d'hidrogen i a un altre àtom de carboni. La fórmula general que representa els compostos que presenten aquest grup funcional és R-CHO. El grup aldehid és electròfil a causa de la deficiència electrònica de l'àtom de carboni. Com en els altres grups funcionals que presenten un grup carbonil, els àtoms d'hidrogen situats en posició α són relativament àcids (en els aldehids pKa ~17) a causa de l'estabilització per ressonància de la base conjugada. Comhdhúile orgánacha iad na haildéid ina bhfuil an grúpa carbóinile −C(H)=O i gceann an tslabhra d'adaimh charbóin. Ó tá dhá nasc oscailte ag an ngrúpa carbóinile, ní mór ceann acu a dhúnadh le hadamh hidrigine H agus an ceann eile ceangailte den tslabhra. Mar sin, is féidir a rá gurb é (nó ) feidhmghrúpa na n-aildéad. Is iad an formaildéad nó an agus an t-aicéataildéad nó an t-eatánal an dá aildéad is simplí. (Mar is léir ón dá shampla seo, is é -ánal is deireadh d'ainmneacha córasacha na n-aildéad, ach bíonn ainmneacha traidisiúnta ar chuid mhór acu agus iad níos coitianta sa litríocht cheimiceach féin ná na hainmneacha córasacha.) Is í an difríocht idir na haildéid agus na céatóin ná go bhfuil an grúpa carbóinile i lár an tslabhra carbóin sna céatóin: cuir i gcomparáid an (an própánal) agus an t-aicéatón (an própánón) , ar isiméirí iad. Bíonn aildéid coitianta go maith sa cheimic orgánach, agus is aildéid iad a lán cumhrán. Is aildéad í an fhanailin a thugann an blas agus an boladh sainiúil don fhanaile, agus is é an cainéaldéad is cúis le blas agus boladh an chainéil. En aldehyd är en organisk förening som innehåller en aldehydgrupp (även kallad formylgrupp). Denna grupp består av en kolatom med dubbelbindning till en syreatom och en väteatom. Gruppen betecknas vanligen -CHO. Den liknar, men är inte samma som ,-OH, som är en alkoholgrupp. Aldehyder bildas när primära alkoholer (försiktigt) oxideras, men oxideras oftast själva vidare till motsvarande karboxylsyra. Närbesläktade till aldehyderna är ketonerna, som bildas då sekundära alkoholer oxideras.Oxidation av tertiära alkoholer kan inte uppstå utan att kolskelettet avspjälkas. 알데하이드(영어: aldehyde 앨더하이드[*] /ˈædəhˌaid/) 또는 알데히드(독일어: aldehyde)는 탄화수소기에 가 첨가된 화학물질의 총칭이다. 분자식은 RCHO이다. 알코올의 불충분한 산화에 의하여 생기며 자극적인 냄새가 나고 포르밀기의 특성상 산화되기 쉬워 은거울반응이나 펠링반응을 일으키며, 산화한 후에는 카르복시산이 된다. 환원제·향료·마취제 등에 쓰인다. الألدهيدات هي صنف من المركبات العضوية التي تحوي مجموعة وظيفية كربونيلية وهي مجموعة فعالة لها دور كبير في التفاعلات الكيميائية، فتكون الصيغة العامة للألدهيدات R-CHO، وبهذا يتميز عن الكيتونات التي تحوي بديلين. ويمثل R في الصيغة ذرة هيدروجين أو جذراً ألكيلياً وإذا أزلنا R من الصيغة العامة للألديهايد فإننا نحصل على مجموعة الفورميل (بالإنجليزية: formyl group)‏. تتم تسمية الالديهايدات الاليفاتيه حسب نظام الايوباك كما يأتي : 1_ يتم تحديد اسم أطول سلسلة كاربونية متصلة (مستمرة) تحتوي على مجموعة ألديهايد. 2_ ترقم السلسلة بحيث تكون ذرة الكاربون في مجموعة الالديهايد رقم 1، وليس هناك داع لتحديد مكانها عند التسمية. Aldehydy (łac. alcohol dehydrogenatus = „alkohol odwodorniony”) – klasa organicznych związków chemicznych posiadających grupę aldehydową, czyli grupę karbonylową (C−O) połączoną z jednym (−CHO) lub dwoma (CH2O) atomami wodoru. Proste aldehydy, będące pochodnymi alkanów i zawierające w cząsteczce jedną grupę aldehydową to alkanale o wzorze ogólnym CnH2n+1CHO. Pokrewną klasę związków stanowią ketony (R2CO), nieposiadające atomu wodoru przy grupie karbonylowej. Ketony i aldehydy mają zbliżone właściwości chemiczne, przy czym aldehydy są z reguły bardziej reaktywne. Istnieje też szereg reakcji charakterystycznych jedynie dla aldehydów.
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageRedirects
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dbr:Dicobalt_octacarbonyl
dbo:wikiPageWikiLink
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Subject Item
dbr:Diethyl_azodicarboxylate
dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Diethylphosphite
dbo:wikiPageWikiLink
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Subject Item
dbr:Diformylcresol
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Aldehyde
Subject Item
dbr:Diisopinocampheylborane
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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gold:hypernym
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dbo:wikiPageWikiLink
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dbo:wikiPageWikiLink
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gold:hypernym
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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wikipedia-en:Aldehyde
foaf:primaryTopic
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