Advertisements
Advertisements
Question
Dipole moment of phenol is smaller than that of methanol. Why?
Advertisements
Solution
In phenol, C – O bond is less polar due to electron-withdrawing effect of benzene ring, whereas in methanol C – O bond is more polar due to electron releasing effect of –CH3 group. Hence, the dipole moment of phenol (1.54 D) is smaller than that of methanol (1.71 D).
APPEARS IN
RELATED QUESTIONS
How do you convert the following:
Ethanol to Propan-2-ol
Give simple chemical test to distinguish between Ethanol and Phenol.
If ethanol dissolves in water, then which of the following would be observed:
Phenol is less acidic than ______.
Out of 2-chloroethanol and ethanol which is more acidic and why?
Suggest a reagent for conversion of ethanol to ethanoic acid.
Arrange water, ethanol and phenol in increasing order of acidity and give reason for your answer.
Match the items of column I with items of column II.
| Column I | Column II | |
| (i) | Methanol | (a) Conversion of phenol to o-hydroxysalicylic acid |
| (ii) | Kolbe’s reaction | (b) Ethyl alcohol |
| (iii) | Williamson’s synthesis | (c) Conversion of phenol to salicylaldehyde |
| (iv) | Conversion of 2° alcohol to ketone | (d) Wood spirit |
| (v) | Reimer-Tiemann reaction | (e) Heated copper at 573 K |
| (vi) | Fermentation | (f) Reaction of alkyl halide with sodium alkoxide |
Assertion: Ethanol is a weaker acid than phenol.
Reason: Sodium ethoxide may be prepared by the reaction of ethanol with aqueous \[\ce{NaOH}\].
Convert the following:
Propanenitrile to ethanol.
Tonics in general contain
Alcoholic fermentation is brought about by the action of
Which of the following is known as wood spirit?
If the starting material is 1-methyl-1,2-epoxy cyclopentane, of absolute configuration, decide which one compound correctly represents the product of its reaction with sodium methoxide in methanol.
How methanol is obtained from methanal.
Give IUPAC names of the following compounds:
\[\begin{array}{cc}
\ce{CH3 - CH - CH - CH - CH2-OH }\\
|\phantom{......}|\phantom{......}|\phantom{.......}\\
\ce{Cl}\phantom{....}\ce{CH3}\phantom{...}\ce{CH3}\phantom{.....}
\end{array}\]
3, 3-dimethyl-1-butene was subject to following reactions:
