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
Arrange the set of compounds in order of increasing boiling points.
Bromomethane, Bromoform, Chloromethane, Dibromomethane.
Which of the following compounds has the highest boiling point?
Which of the following possesses the highest melting point?
Which is the correct increasing order of boiling points of the following compounds?
1-Iodobutane, 1-Bromobutane, 1-Chlorobutane, Butane
Out of o-and p-dibromobenzene which one has higher melting point and why?
Which of the following compounds will have the highest melting point and why?
| (I) | ![]() |
|
(II) |
![]() |
| (III) | ![]() |
Which out of the following is an intensive property?
Arrange the isomeric dichlorobenzene in the increasing order of their boiling point and melting points.
Write the structure of the following organic halogen compound.
4-tert-Butyl-3-iodoheptane
Write the structure of the following organic halogen compound:
4-tert-Butyl-3-iodoheptane



