Advertisements
Advertisements
Question
Explain why is \[\ce{O = C =O}\] nonpolar while \[\ce{R - O - R}\] is polar.
Advertisements
Solution
\[\ce{O = C =O}\] molecule is linear so that the polarities of two C – O bonds get cancelled and the molecule is linear.
Ethers have structures similar to water and have angular or bent structure. Therefore, the polarity of two R – O groups does not get cancelled and these have net dipole moment. Thus, \[\ce{R - O - R}\] is polar.


APPEARS IN
RELATED QUESTIONS
Write the structure of the compound whose IUPAC name is as follows:
2,3-Diethylphenol
Write the structure of the compound whose IUPAC name is as follows:
Cyclohexylmethanol
Write the structure of the compound whose IUPAC name is as follows:
3-Cyclohexylpentan-3-ol
Which one of the following are correctly arranged on the basis of the property indicated?
When phenol is treated with bromine water, white precipitate is obtained. Give the structure and the name of the compound formed.
Which of the following does not form phenol or peroxide?
Epoxides are
4 – chloro – 3, 5 – dimethyl phenol is called
Glycerol is used
Diethyl ether finds are in medicine as
Ether can be used
Wine (alcoholic beverages) contains
\[\begin{array}{cc}\phantom{......}\ce{OH}\\
\phantom{....}|\\\ce{CH3CH2 - C - CH3}\\
\phantom{....}|\\\phantom{.....}\ce{Ph}\end{array}\] cannot be prepared by ______.
Why is the C-O bond length in phenols less than that in methanol?
Total number of possible isomers (both structural as well as stereoisomers) of cyclic ethers of molecular formula C4H8O is ______.
