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प्रश्न
Why is the C – O – H bond angle in alcohols slightly less than the tetrahedral angle whereas the C – O – C bond angle in ether is slightly greater?
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उत्तर
The C – O – H bond angle in alcohols is slightly less than the tetrahedral angle (109.5°) because of larger repulsions between the lone pairs of electrons. For example in methanol C – O – H bond angle is 108.9°.
In ethers, the C – O – C bond angle is slightly greater than tetrahedral angle. For example in dimethyl ether C – O – C bond angle is 111.7°. The larger bond angle in ethers may be because of greater repulsions between bulkier alkyl groups as compared to one H in alcohols.
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संबंधित प्रश्न
Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.
Give the equation of the following reaction:
Treating phenol with chloroform in the presence of aqueous NaOH.
Write the mechanism of acid-catalysed dehydration of ethanol to yield ethene.
Name the reagent used in the following reaction:
Oxidation of a primary alcohol to aldehyde.
Write the mechanism (using curved arrow notation) of the following reaction :

In the reduction \[\ce{R - CHO + H2 -> RCH2OH}\] the catalyst used is:
By which of the following methods alcohol can be prepared in excellent yield?
Which of the following are used to convert RCHO into RCH2OH?
(i) H2/Pd
(ii) LiAlH4
(iii) NaBH4
(iv) Reaction with RMgX followed by hydrolysis
Dehydration of 2-butanol yields:
Which one of the following on oxidation gives a ketone?
Identify the secondary alcohols from the following set:
- \[\ce{CH3CH2CH(OH)CH3}\]
- \[\ce{(C2H5)3COH}\]


The process of converting alkyl halides into alcohols involves ______.
Suggest a reagent for the following conversion.

In Kolbe’s reaction, instead of phenol, phenoxide ion is treated with carbon dioxide. Why?
What is Lucas reagent?
Write the mechanism of acid-catalysed dehydration of ethanol to yield ethene.
Write the mechanism of acid dehydration of ethanol to yield ethene.
Write the mechanism of acid-catalysed dehydration of ethanol to yield ethene.
