In a set of the given reactions, acetic acid yielded a product C.Product C would be
CH3CH(OH)C6H5
CH3CH(OH)C2H5
CH3COC6H5
Reduction by LiAIH4 of hydrolysed product of an ester gives
two acids
two aldehydes
one molecule of alcohol and another of carboxylic acid
two alcohols
Consider the following transformationsThe molecular formula of C is
ICH2-COCH3
CHI3
CH3I
Self condensation of two moles of ethyl acetate in presence of sodium ethoxide yields
ethyl butyrate
acetoacetic ester
methyl acetoacetate
ethyl propionate
Which one of the following esters cannot undergo Claisen self-condensation ?
CH3CH2CH2CH2COOC2H5
C6H5COOC2H5
C6H5CH2COOC2H5
C6H11CH2COOC2H5
Sodium formate on heating yields
oxalic acid and H2
Sodium oxalate and H2
CO2 and NaOH
Sodium oxalate
Benzoic acid may be converted into ethyl benzoate by reaction with
sodium ethoxide
ethyl chloride
dry HCI, C2H5OH
ethanol
An ester is boiled with KOH. The product is cooled and acidified with conc HCI. A white crystalline acid separates. The ester is
methyl acetate
ethyl acetate
ethyl formate
ethyl benzoate
Among the following the strongest acid is
CH3COOH
CH2 CICH2COOH
CH2 CICOOH
CH3CH2COOH
Propionic acid with Br2 - P yields a dibromo product. Its structure would be
CH2 Br-CHBr-COOH
CH2Br-CH-COBr
