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
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
D.
methoxyethane
Molecular formula C3H8O (CnH2n+2O) suggests that the organic compound is either alcohol or ether.
Since, the compound on reaction with HI gives two different compounds, it must be an unsymmetrical ether, and its formula must be CH3OC2H5 (methoxyethane).
The reaction are as follows
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