The letter 'D' in D-glucose signifies
configuration at all chiral carbons
dextrorotatory
that it is a monosaccharide
configuration at a particular chiral carbon
D.
configuration at a particular chiral carbon
Letter 'D' before the name of monosaccharide reveals that the -OH group at the second carbon atom is towards the right e, it only shows the configuration 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
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