Raymond Wright Johnson has written:

'The velocity of hydrolysis of stereoisomeric hydrazones and oximes' -- subject(s): Hydrazines, Hydrazones, Hydrolysis, Oxides, Oximes

one of them has the OH group in its right hand butanother has it on the left hand. but i wanna know what is their name

Due to resonance between lone pair of electrons on the O- atom of the -OH group and C=O group the carboxyl carbon is less electrophilic than the carbonyl carbon in aldehyde or ketone. Therefore, nucleopihilic addition of hydroxylamine (NH2OH) to the C=O group of carboxylic acid does not occur and hence it does not form oximes.

Ismail Ekcan has written:

'Metal complexes of selected 5-Alkylamino-1,2-benzoquinone-2-oximes and their applicability in solvent extraction'

John Frank Marcoccia has written:

'An ab initio study on the protonation of simple aliphatic oximes in their ground and low-lying valence excited states'