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प्रश्न
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
Butan-1-ol
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उत्तर
\[\ce{CH3CH2CH2CH2OH + HCl_{(conc.)} ->[ZnCl2] No reaction at room temperature}\]
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संबंधित प्रश्न
Give two reactions that show the acidic nature of phenol.
Explain how does the −OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
Phenols do not react with one of the following:
The ionization constant of phenol is higher than that of ethanol because ____________.
In CH3CH2OH, the bond that undergoes heterolytical change most readily is ____________.
Strength of acidity is in order:
Which of the following compounds is most acidic?
Which one of the following compounds has the most acid nature?
Mark the correct order of decreasing acid strength of the following compounds.
| (a) |  |
| (b) |  |
| (c) |  |
| (d) |  |
| (e) |  |
Assertion: o-Nitrophenol is less soluble in water than the m- and p-isomers.
Reason: m- and p- Nitrophenols exist as associated molecules.
Arrange the following in the increasing order of their property indicated:
4-Nitrobenzoic acid, benzoic acid, 3,4-Dinitrobenzoic acid, 4-Methoxy benzoic acid (Acid strength)
Which is the final product ‘A’ (major) in the given reaction?
For the pair phenol and cyclohexanol, answer the following:
Why is phenol more acidic than cyclohexanol?
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
2-Methylbutan-2-ol
Give the structure of the product you would expect when the following alcohol reacts with HBr.
Butan-1-ol
Give the structure of the product you would expect when the following alcohol reacts with SOCl2.
2-Methylbutan-2-ol
