Advertisements
Advertisements
प्रश्न
Why dextro and laevorotatory isomers of Butan-2-ol are difficult to separate by fractional distillation?
Advertisements
उत्तर
Dextro and laevorotatory isomers of Butan-2-ol are enantiomers of each other and both have the same boiling point and hence they cannot be separated by fractional distillation.
APPEARS IN
संबंधित प्रश्न
p-Dichlorobenzene has higher m.p. and lower solubility than those of o- and m-isomers. Discuss.
Define racemic mixture.
Which of the following compounds has the highest boiling point?
How many structural isomers are possible for a compound with the molecular formula C3H7Cl?
Which of the following possesses the highest melting point?
Mg reacts with RBr best in ____________.
Which is the correct increasing order of boiling points of the following compounds?
1-Iodobutane, 1-Bromobutane, 1-Chlorobutane, Butane
Which is the correct increasing order of boiling points of the following compounds?
1-Bromoethane, 1-Bromopropane, 1-Bromobutane, Bromobenzene
Why is the boiling point of o-dichlorobenzene higher than p-dichlorobenzene, but the melting point of para-isomer is higher than ortho-isomer?
Write the structure of the following organic halogen compound.
4-tert-Butyl-3-iodoheptane
