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Published byClementine Dickerson Modified over 9 years ago
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Aldehydes and Ketones Functional group formula? C=O F.G. name? The carbonyl group
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Naming Aldehydes – how can you spot one? (C=O on the end of the chain i.e. C N o 1) end in ……al Ketones (C=O has C’s on both sides) end in ….one Position of C=O given as a number What is the largest chain where a number is not required? Butanone – 4 C’s Try 1,1,1-trifluoropentan-2-one 1-hydroxyhex-2-ene-4-one Watch out for benzaldehyde and phenylethanone
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Reduction of Aldehydes and Ketones to Alcohols Reagents NaBH 4 (sodium borohydride) – a source of hydride (H - ions) then dilute sulphuric acid Conditions Room temperature Another source of H - ? LiAlH 4
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Equation CH 3 CHO + 2[H] CH 3 CH 2 OH Draw a diagram showing how the reactants relate to the products Repeat the equation and diagram for propanone See questions page 17 of notes
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How does it happen? The mechanism shows this What factors do you consider when trying to work out a mechanism? Polarity of bonds Areas of positive or negative charge Characteristics of particles present in the reactants – NaBH 4 is a source of H -.
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Reduction mechanism – addition of hydrogen
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How does it happen? Conditions – are free radicals likely to be formed? KCN contains which particles? K + and CN - (dot/cross diagram?) What do acids do? Try to create a mechanism (consider ethanal). Check names of products and note that in all cases a 2-hydroxy compound is formed See q’s page 18
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Oxidation of Aldehydes Remember that ketones are not readily oxidised Extension note – ketones can be oxidised, but only under relatively severe conditions, where the carbon chain is broken. They are flammable ( burning= oxidation)
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Oxidation of Aldehydes Reagents K 2 Cr 2 O 7 / sulphuric acid K 2 Cr 2 O 7 = potassium dichromate Conditions H&R When do you heat and distil?
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Oxidation of Aldehydes Equation RCHO + [O] RCOOH Draw a diagram to illustrate this (not a mechanism) See Q,s page 20
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Tests for Aldehydes/ketones 2,4-dinitrophenylhydrazine Test for? Carbonyl group C=O Observation? Orange precipitate
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