CARBONYL COMPOUNDS AND CARBOHYDRATES
HYDROLYSIS OF POLYSACCHARIDES
-
-
Susceptible to both nucleophiles and electrophiles
Presence of C=O
TEST FOR ALDEHYDES AND KETONES
-
-
Reaction with 2,4-DNP (Dinitrophenylhydrazine)
Positive: Formation of yellow precipitate
IODOFORM TEST
-
Carbonyl compounds: Methyl ketones will give a positive result
Postive: Yellow precipitate (CHI3)
MOLISCH’S TEST for carbohydrates
-
TOLLEN’S TEST – for aldehydes
-
-
Test for easily oxidizable compounds (ex.
Aldehydes)
Positive: Silver mirror deposit
-
-
Polyhydroxyaldehydes (aldoses)
Polyhydroxyketones (ketoses)
-
Classifications:
Test for reducing sugars
Reagent: CuSO4, sodium citrate and sodium carbonate in a mildly basic solution
Positive test: Brick red precipitate
OSAZONE TEST
1. Simple - monosaccharides
2. Complex – disaccharides, polysaccharides
-
Hemiacetals/Hemiketals
-
Dehydration test to identify carbohydrates from non-carbohydrates Reagent: Molisch reagent (10% α-napthol in ethanol) and conc. H2SO4
Positive test: Purple ring at the interface of two layers for all carbohydrates.
BENEDICT’S TEST
CARBOHYDRATES
-
Starch Glucose
- Starch is a polymer of D-glucose units bound by glycosidic linkages.
Cellulose Glucose
- Breakage of the β-1,4-glycosidic bonds by acids leads to the hydrolysis of cellulose polymers, resulting in the sugar molecule glucose or oligosaccharides.
-
Intramolecular reaction: C = O group and one of the
–OH groups
Test for carbohydrates; time for the formation of osazone gives an idea for the identity of the sugar.
Reagent: phenylhydrazine-HCl/NaCH3COOH
Positive test: yellow crystals
ACYL COMPOUNDS, SOAPS AND DETERGENTS
SIMPLE SUGARS (monosaccharides)
-
Cannot be converted into smaller sugars by hydrolysis Glucose, fructose
Undergo nucleophilic substitution
Benzoic Acid - Soluble in hot water,