The letter 'D' in D-glucose signifies
configuration at all chiral carbons
dextrorotatory
that it is a monosaccharide
configuration at a particular chiral carbon
Reaction of methyl bromide with aqueous sodium hydroxide involves
racemisation
SN 1 mechanism
retention of configuration
SN 2 mechanism
Benzaldehyde and acetone can be best distinguished using
Fehling's solution
Sodium hydroxide solution
2, 4-DNP
Tollen's reagent
D.
Tollen's reagent
With Fehling's solution, benzaldehyde as well as acetone do not react while with Tollen's reagent, benzaldehyde gives precipitate but acetone does not react. Hence, Tollen's reagent is used to distinguish them.
Phenol forms a tribromo derivative, 'X' is
bromine in benzene
bromine in water
potassium bromide solution
bromine in carbon tetrachloride at 0°C
One mole of an organic compound A with the formula C3H8O reacts completely With two moles of HI to form X and Y. When Y is boiled with aqueous alkali it forms Z. Z answers the iodoform test. The compound A is
propan-2-ol
propan-1-ol
ethoxyethane
methoxyethane
The correct sequence ofsteps involved in the mechanism of Cannizaro's reaction is
nucleophilic attack, transfer of H- and transfer of H+
transfer of H-, transfer of H+ and nucleophilic attack
transfer if H+, nucleophilic attack and transfer of H-
electrophilic attack by OH-, transfer of H+ and transfer of H-
The IUPAC name of
2-methyl-3-bromohexanal
3-bromo-2-methylbutanal
2-methyl-3-bromobutanal
3-bromo-2-methylpentanal
Which one of the following forms propane nitrile as the major product?
Ethyl bromide + alcoholic KCN
Propyl bromide + alcoholic KCN
Propyl bromide + alcoholic AgCN
Ethyl bromide + alcoholic AgCN