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By: Kendra & Ashley. General Structure Carbon double bonded to oxygen with two hydrocarbon groups (alkyl groups) Ketones never have a hydrogen atom attached.

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Presentation on theme: "By: Kendra & Ashley. General Structure Carbon double bonded to oxygen with two hydrocarbon groups (alkyl groups) Ketones never have a hydrogen atom attached."— Presentation transcript:

1 By: Kendra & Ashley

2 General Structure Carbon double bonded to oxygen with two hydrocarbon groups (alkyl groups) Ketones never have a hydrogen atom attached to the carbonyl group

3 IUPAC Names for Ketones the -e ending of the parent alkane is replaced with the -one suffix of the ketone family The location of the carbonyl carbon is indicated with a number. The longest carbon chain is numbered to give the carbonyl carbon the lowest possible number. The alkyl groups are listed alphabetically or in order of increasing size.

4 Common Names acetone acetophenone benzophenone

5 2-butanone2-chloro-4-methyl-3-pentanone 1-phenyl-1-butanone 4-methyl-2-cyclohexen-1-one Examples

6 3-methyl-2-butanone 3-bromocyclohexanone 4-hydroxy-3-methyl-2-butanone Examples

7 Benedict's test The Benedict's test differentiates aldehydes and ketones. Aldehydes can be oxidized by Cu2+ in the presence of a strong base to form carbonic acids. Ketones cannot be oxidized by this reaction. When the Cu2+ oxidizes the aldehydes it is reduced to Cu+, and forms the compound Cu2O, which is a reddish precipitate. That is how you know you have an aldehyde. If it doesn’t turn red, you know you have a ketone.

8 Tollen’s test The Tollen’s test, is a basic solution of Ag(NH3)+. The Silver (I) cation is reduced (gains one electron) at the same time the aldehyde is oxidized. This produces metallic silver (Ag0), which often forms a shiny “mirror” look. Thus Tollens’ reagent can be used to detect the presence of an aldehyde functional group – if a mirror forms then the compound tested is an aldehyde. If the test fails, then the compound is a ketone.

9 Hydrazine test Hydrazine test can be used to detect ketones. When treated with 2,4 - dinitrophenyl hydrazine, ketones are converted to their respective hydrazones, due to the presence of the carbonyl group, and an yellow or orange precipitate is observed. Hydrazones have a sharp melting point, and can be used to detect the original ketone.

10 Everyday Uses Carvone = spearmint flavouring Acetone = Nail polish remover, paint thinner, & cleaning solvents Demascone = berry flavouring Octanone = mushroom flavouring Benzophenone = perfume & sunscreen

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