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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? - Chemistry

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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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पाठ 11: Alcohols, Phenols and Ethers - Multiple Choice Questions (Type - I) [पृष्ठ १६०]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
पाठ 11 Alcohols, Phenols and Ethers
Multiple Choice Questions (Type - I) | Q 51 | पृष्ठ १६०

संबंधित प्रश्‍न

Write the mechanism of the following reaction:


Write the mechanism of the following reaction :


Give the equation of the following reaction:

Oxidation of propan-1-ol with alkaline KMnO4 solution.


Name the reagent used in the following reaction:

Oxidation of a primary alcohol to aldehyde.


Name the reagent used in the following reaction:

Benzyl alcohol to benzoic acid.


Lucas reagent is ____________.


Lucas test is used for the detection of _____________.


Which one of the following on oxidation gives a ketone?


\[\ce{CH3CH2OH}\] can be converted into \[\ce{CH3CHO}\] by ______.


Identify the secondary alcohols from the following set:

  1. \[\ce{CH3CH2CH(OH)CH3}\]
  2. \[\ce{(C2H5)3COH}\]



Alcohols react with active metals e.g. Na, K etc. to give corresponding alkoxides. Write down the decreasing order of reactivity of sodium metal towards primary, secondary and tertiary alcohols.


Ethers can be prepared by Williamson synthesis in which an alkyl halide is reacted with sodium alkoxide. Di-tert-butyl ether can’t be prepared by this method. Explain.


Which of the following alcohols will not undergo oxidation?


Write the mechanism of acid dehydration of ethanol to yield ethene.


Write the mechanism of acid dehydration of ethanol to yield ethene.


Write the mechanism of acid dehydration of ethanol to yield ethene.


Write the mechanism of acid 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.


Write the mechanism of acid-catalysed dehydration of ethanol to yield ethene


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