Advertisements
Advertisements
Question
Why alkyl halides though polar are immiscible with water?
Advertisements
Solution
Alkyl halides are polar molecules, therefore, their molecules are held together by dipole-dipole attraction. The molecules of H2O are held together by H-bonds. Since the new forces of attraction between water and alkyl halide molecules are weaker than the force of attraction already existing between alkyl halide - alkyl halide molecules and water - water molecules therefore alkyl halides are immiscible (not soluble) in water. Alkyl halide are neither able to form H-bonds with water nor able to break the H-bonding network of water.
APPEARS IN
RELATED QUESTIONS
Give reasons : n-Butyl bromide has higher boiling point than t-butyl bromide.
Arrange the set of compounds in order of increasing boiling points.
Bromomethane, Bromoform, Chloromethane, Dibromomethane.
Explain why alkyl halides, though polar, are immiscible with water?
p-Dichlorobenzene has higher m.p. and lower solubility than those of o- and m-isomers. Discuss.
For the same alkyl group, an alkyl bromide has a higher boiling point than alkyl fluoride because:
Which of the following compounds has the highest boiling point?
Which of the following halide is 2°?
Which of the following is liquid at room temperature (b.p. is shown against it)?
Which of the following possesses the highest melting point?
Mg reacts with RBr best in ____________.
p-dichlorobenzene has a higher melting point than its o- and m-isomers because ____________.
Arrange the following compounds in the increasing order of their densities.
(a)

(b)

(c)

(d)

Arrange the following compounds in increasing order of their boiling points.
(a) \[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
\backslash\phantom{...........}\\
\ce{CH - CH - CH2Br}\\
/\phantom{.............}\\
\ce{CH3}\phantom{..................}
\end{array}\]
(b) \[\ce{CH3CH2CH2CH2Br}\]
(c) \[\begin{array}{cc}
\phantom{...}\ce{CH3}\\
\phantom{}|\\
\ce{H3C - C - CH3}\\
\phantom{}|\\
\phantom{..}\ce{Br}
\end{array}\]
Reaction of \[\ce{C6H5CH2Br}\] with aqueous sodium hydroxide follows ______.
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 following compounds in increasing order of their boiling points:
CH3CH2OH, CH3−CHO, CH3−COOH
Why is the boiling point of o-dichlorobenzene higher than p-dichlorobenzene, but the melting point of para-isomer is higher than ortho-isomer?
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
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



