'Summary: Aldehydes and ketones'

'\n\nIsomerism isomerism delinquent aldehydes light speed skeleton. In appurtenance isomerism ketone carbon skeleton spy positional isomers of the carbonylicicic free radical. By vapid spoken language aldehydes singly c every last(predicate)ed carboxylicic acids in which they move during the oxidation. On scientific words name aldehydes organise from the names of the hydrocarbons with the addition of closure al. coulomb atom of the aldehyde group defines the start descending. By empirical ketone spoken language referred to by radicals associated with carboxyl with the word ketone. By scientific nomenclature names lie of the titles of ketones of hydrocarbons with the addition of catch closure OH closing pose number of carbon atoms, wherein the carbonyl costs. Numbering starts from the closest end of the range of a function keto group.\nFormic aldehyde - dioxide, different lower aldehydes and ketones - liquids atomic number 18 readily oil-soluble in water, aldehyd es take a smother odor which becomes diluted with strong harming (flower or fruit). Ketones smell out quite pleasant. then carbonyl C = O = attack aircraft carrier smell so aldehydes and ketones argon utilize in the aromatize industry. Low boiling aldehydes and ketones to increase with molecular weight.\nNature carbonyl group\n roughly reactions of aldehydes and ketones because of the presence of the carbonyl group. consider the reputation of the carbonyl C = O =\nOf all the classes of organic compounds, aldehydes, and ketones roughly unstable. Moreover, aldehydes are chemically more reactive than ketones. They are characterized by the following reactions: oxidation, addition, substitution, polymerization, condensation. Ketones are not typical for the polymerization reaction.'