Secondary nitroalkanes can be converted into ketones by using Y. Identify Y from the following
aqueous HCl
aqueous NaOH
KMnO4
CO
Alkyl cyanides undergo Stephen reduction to produce
aldehyde
secondary amine
primary amine
amide
Reaction of PCl3 and PhMgBr would give
bromobenzene
chlorobenzene
triphenylphosphine
dichlorobenzene
Ethylene glycol gives oxalic acid on oxidation with
acidified K2Cr2O7
acidified KMnO4
alkaline KMnO4
periodic acid
A Wittig reaction with an aldehyde gives
ketone compound
a long chain fatty acid
olefin compound
epoxide
C.
olefin compound
This is also a mean of preparing alkene where the position of the double bond is definite. In Wittig reaction, aldehyde (-CHO) and ketone react with methylene triphenyl phosphine
Maleic acid and fumaric acid are
position isomers
geometric isomers
enantiomers
functional isomers
Give the IUPAC name for
ethyl-4-oxoheptanoate
methyl-4-oxoheptanoate
ethyl-4-oxohexanoate
methyl-4-oxohexanoate